Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1479 |
|---|---|
| ensemblid | ENSG00000176102.13 |
| hgncid | 2485 |
| symbol | CSTF3 |
| name | cleavage stimulation factor subunit 3 |
| refseq_nuc | NM_001326.3 |
| refseq_prot | NP_001317.1 |
| ensembl_nuc | ENST00000323959.9 |
| ensembl_prot | ENSP00000315791.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 33084584 |
| end | 33161480 |
| strand | - |
| ver | v1.2 |
| region | chr11:33084584-33161480 |
| region5000 | chr11:33079584-33166480 |
| regionname0 | CSTF3_chr11_33084584_33161480 |
| regionname5000 | CSTF3_chr11_33079584_33166480 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 717 | 360 | 90 | 56 | 170 | 14 | 28 | 132 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2154 | 353 | 90 | 49 | 170 | 14 | 28 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| c0002 | 0/0 | 2154 | 4 | 0 | 4 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| c0003 | 0/0 | 2154 | 3 | 0 | 3 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 659 | 149 | 68 | 16 | 49 | 6 | 9 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| t0002 | 0/0 | 659 | 111 | 10 | 22 | 64 | 2 | 13 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| t0003 | 0/1 | 659 | 91 | 12 | 17 | 50 | 6 | 5 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| t0004 | 0/0 | 659 | 6 | 0 | 0 | 6 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| t0005 | 0/0 | 659 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| t0006 | 0/0 | 659 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| t0007 | 0/0 | 659 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0005 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0010 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2154 | 353 | 90 | 49 | 170 | 14 | 28 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0002 | 0/0 | 2154 | 4 | 0 | 4 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0003 | 0/0 | 2154 | 3 | 0 | 3 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2812 | 149 | 68 | 16 | 49 | 6 | 9 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0001t0002 | 0/0 | 2812 | 104 | 10 | 15 | 64 | 2 | 13 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0001t0003 | 0/1 | 2812 | 91 | 12 | 17 | 50 | 6 | 5 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0001t0004 | 0/0 | 2812 | 6 | 0 | 0 | 6 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0001t0005 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0001t0006 | 0/0 | 2812 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0001t0007 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0002t0002 | 0/0 | 2812 | 4 | 0 | 4 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| a0001c0003t0002 | 0/0 | 2812 | 3 | 0 | 3 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | copy fasta | chr11 | 33079584 | 33166480 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0010 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0005 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0002t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0003t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0003t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0128 | EUR | GBR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | GBR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | FIN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | FIN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0132 | EUR | FIN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0014 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0014 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0193 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0017 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0064 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0167 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0017 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0118 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | CDX | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CDX | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CDX | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | CDX | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0024 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0174 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0134 | EUR | TSI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | GIH | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | GIH | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | USA | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | USA | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | USA | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | USA | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0126 | REF | REF | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0010 | REF | REF | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:33090595
|
A | G | 1 | a0001c0002 | 4 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
synonymous_variant | LOW | c.1578T>C | p.Asp526Asp | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/21 | 1733/2812 | 1578/2154 | 526/717 | chr11 | 33090595 | ||
| chr11:33099620
|
G | A | 1 | a0001c0003 | 3 | HG01070.hp1 HG01071.hp2 HG02300.hp1 |
synonymous_variant | LOW | c.924C>T | p.Leu308Leu | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 11/21 | 1079/2812 | 924/2154 | 308/717 | chr11 | 33099620 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:33084710
|
A | G | 1 | a0001c0001t0006 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 21/21 | 377 | chr11 | 33084710 | |||||
| chr11:33085070
|
C | T | 2 | a0001c0001t0003a0001c0001t0006 | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*17G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 21/21 | 17 | chr11 | 33085070 | |||||
| chr11:33161377
|
A | G | 1 | a0001c0001t0007 | 1 | HG01433.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/21 | 52 | chr11 | 33161377 | |||||
| chr11:33161395
|
A | G | 1 | a0001c0001t0004 | 6 | HG00423.hp1 HG02135.hp1 NA18945.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-70T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/21 | 70 | chr11 | 33161395 | |||||
| chr11:33161422
|
C | G | 1 | a0001c0001t0005 | 1 | NA18942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-97G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/21 | 97 | chr11 | 33161422 | |||||
| chr11:33161471
|
A | G | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(3): Show | 204 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-146T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/21 | chr11 | 33161471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:33085320
|
CAT | C | 15 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0202others(12): Show | 15 | HG00280.hp1 HG00733.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1952-33_1952-32del others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 20/20 | chr11 | 33085320 | ||||||
| chr11:33085362
|
C | CTTTATAG | 202 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(199): Show | 225 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1952-74_1952-73ins others(7): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 20/20 | chr11 | 33085362 | ||||||
| chr11:33085556
|
T | C | 226 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(223): Show | 249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1951+157A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 20/20 | chr11 | 33085556 | ||||||
| chr11:33085660
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1951+53G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 20/20 | chr11 | 33085660 | ||||||
| chr11:33086018
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1796-29C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086018 | ||||||
| chr11:33086146
|
C | CAG | 235 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0195others(232): Show | 259 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1796-159_1796-158d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086146 | ||||||
| chr11:33086287
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1796-298A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086287 | ||||||
| chr11:33086304
|
A | G | 1 | a0001c0001t0006g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1796-315T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086304 | ||||||
| chr11:33086442
|
C | CT | 124 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(121): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1796-454dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086442 | ||||||
| chr11:33086442
|
C | CTT | 88 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(85): Show | 94 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1796-455_1796-454d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086442 | ||||||
| chr11:33086442
|
C | CTTT | 6 | a0001c0001t0002g0018a0001c0001t0002g0029a0001c0001t0002g0063others(3): Show | 7 | HG00597.hp1 HG01261.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1796-456_1796-454d others(5): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086442 | ||||||
| chr11:33086468
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1796-479C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086468 | ||||||
| chr11:33086524
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1795+464C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086524 | ||||||
| chr11:33086571
|
G | A | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1795+417C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086571 | ||||||
| chr11:33086623
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1795+365T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086623 | ||||||
| chr11:33086700
|
A | T | 1 | a0001c0001t0003g0188 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1795+288T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086700 | ||||||
| chr11:33086704
|
C | T | 1 | a0001c0001t0003g0116 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1795+284G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086704 | ||||||
| chr11:33086720
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1795+268T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086720 | ||||||
| chr11:33087955
|
C | T | 90 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0106others(87): Show | 106 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1642-814G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33087955 | ||||||
| chr11:33088213
|
C | CTT | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1642-1073_1642-107 others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088213 | ||||||
| chr11:33088219
|
A | G | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1642-1078T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088219 | ||||||
| chr11:33088289
|
C | CT | 43 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(40): Show | 43 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1642-1149dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088289 | ||||||
| chr11:33088429
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1642-1288G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088429 | ||||||
| chr11:33088564
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1642-1423C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088564 | ||||||
| chr11:33088583
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1642-1442T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088583 | ||||||
| chr11:33088680
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1642-1539T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088680 | ||||||
| chr11:33088714
|
G | T | 1 | a0001c0001t0003g0122 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1642-1573C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088714 | ||||||
| chr11:33088731
|
C | T | 90 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0106others(87): Show | 106 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1642-1590G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088731 | ||||||
| chr11:33088772
|
A | G | 5 | a0001c0001t0002g0054a0001c0001t0002g0059a0001c0001t0002g0061others(2): Show | 5 | HG02165.hp1 NA18978.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1642-1631T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088772 | ||||||
| chr11:33088881
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1641+1651C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088881 | ||||||
| chr11:33089276
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1641+1256C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089276 | ||||||
| chr11:33089344
|
C | CA | 88 | a0001c0001t0002g0006a0001c0001t0002g0047a0001c0001t0002g0103others(85): Show | 106 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1641+1187dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089344 | ||||||
| chr11:33089344
|
CA | C | 52 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0195others(49): Show | 53 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1641+1187delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089344 | ||||||
| chr11:33089386
|
A | G | 2 | a0001c0001t0002g0110a0001c0001t0002g0159 | 2 | NA18967.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1641+1146T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089386 | ||||||
| chr11:33089697
|
T | C | 2 | a0001c0001t0002g0054a0001c0001t0002g0061 | 2 | NA18978.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1641+835A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089697 | ||||||
| chr11:33089828
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1641+704A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089828 | ||||||
| chr11:33089894
|
G | C | 1 | a0001c0001t0002g0076 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1641+638C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089894 | ||||||
| chr11:33089941
|
A | G | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1641+591T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089941 | ||||||
| chr11:33090035
|
A | G | 92 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0106others(89): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1641+497T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33090035 | ||||||
| chr11:33090275
|
T | G | 1 | a0001c0001t0002g0103 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1641+257A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33090275 | ||||||
| chr11:33090491
|
GA | G | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1641+40delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33090491 | ||||||
| chr11:33090855
|
A | AT | 42 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0019others(39): Show | 51 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1446-129dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33090855 | ||||||
| chr11:33091267
|
A | G | 1 | a0001c0001t0002g0012 | 2 | NA18965.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1446-540T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091267 | ||||||
| chr11:33091357
|
A | C | 177 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(174): Show | 199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1446-630T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091357 | ||||||
| chr11:33091376
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1446-649A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091376 | ||||||
| chr11:33091564
|
C | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1445+707G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091564 | ||||||
| chr11:33091576
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0044 | 3 | NA18965.hp2 NA18986.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1445+695C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091576 | ||||||
| chr11:33091609
|
T | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1445+662A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091609 | ||||||
| chr11:33091610
|
G | A | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1445+661C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091610 | ||||||
| chr11:33091758
|
G | T | 4 | a0001c0001t0002g0103a0001c0001t0002g0129a0001c0001t0002g0130others(1): Show | 4 | HG03688.hp2 NA18979.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1445+513C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091758 | ||||||
| chr11:33091832
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1445+439G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091832 | ||||||
| chr11:33091953
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0173 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1445+318G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091953 | ||||||
| chr11:33092066
|
T | G | 2 | a0001c0001t0002g0162a0001c0001t0002g0173 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1445+205A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092066 | ||||||
| chr11:33092084
|
CTG | C | 3 | a0001c0001t0001g0263a0001c0001t0001g0310a0001c0001t0001g0316 | 3 | HG01069.hp1 HG03239.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1445+185_1445+186d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092084 | ||||||
| chr11:33092107
|
T | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1445+164A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092107 | ||||||
| chr11:33092156
|
G | A | 20 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0199others(17): Show | 20 | HG00642.hp2 HG01109.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1445+115C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092156 | ||||||
| chr11:33092211
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1445+60T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092211 | ||||||
| chr11:33092364
|
A | AT | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(175): Show | 201 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1376-25dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092364 | ||||||
| chr11:33092371
|
T | A | 1 | a0001c0001t0001g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1376-31A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092371 | ||||||
| chr11:33092403
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0315 | 3 | HG00735.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1376-63A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092403 | ||||||
| chr11:33092596
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1376-256A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092596 | ||||||
| chr11:33092612
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1376-272A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092612 | ||||||
| chr11:33093011
|
T | A | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1376-671A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33093011 | ||||||
| chr11:33093244
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1376-904T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33093244 | ||||||
| chr11:33093869
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0089 | 2 | HG00423.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1376-1529C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33093869 | ||||||
| chr11:33093926
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1376-1586A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33093926 | ||||||
| chr11:33094298
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1376-1958A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094298 | ||||||
| chr11:33094355
|
A | G | 4 | a0001c0001t0003g0028a0001c0001t0003g0123a0001c0001t0003g0131others(1): Show | 4 | HG02080.hp1 NA18939.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375+1951T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094355 | ||||||
| chr11:33094415
|
C | T | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1375+1891G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094415 | ||||||
| chr11:33094508
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0311a0001c0001t0001g0312others(3): Show | 7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1375+1798C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094508 | ||||||
| chr11:33094706
|
C | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 7 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1375+1600G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094706 | ||||||
| chr11:33094841
|
ATTTC | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1375+1461_1375+146 others(8): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094841 | ||||||
| chr11:33095196
|
G | A | 1 | a0001c0001t0003g0188 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1375+1110C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095196 | ||||||
| chr11:33095414
|
C | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1375+892G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095414 | ||||||
| chr11:33095444
|
A | G | 92 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0106others(89): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1375+862T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095444 | ||||||
| chr11:33095587
|
C | T | 2 | a0001c0001t0002g0087a0001c0001t0002g0098 | 2 | NA18951.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1375+719G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095587 | ||||||
| chr11:33095597
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1375+709C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095597 | ||||||
| chr11:33095622
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1375+684G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095622 | ||||||
| chr11:33095648
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1375+658A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095648 | ||||||
| chr11:33095678
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1375+628C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095678 | ||||||
| chr11:33095814
|
T | C | 236 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0195others(233): Show | 260 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1375+492A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095814 | ||||||
| chr11:33095819
|
C | CA | 93 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0085others(90): Show | 112 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1375+486dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | ||||||
| chr11:33095819
|
C | CAA | 82 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(79): Show | 86 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1375+485_1375+486d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | ||||||
| chr11:33095819
|
C | CAAAT | 41 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0019others(38): Show | 49 | HG00438.hp1 HG00733.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1375+483_1375+486d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | ||||||
| chr11:33095819
|
C | CAAATAAA others(1): Show |
25 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0197others(22): Show | 25 | HG00280.hp1 HG00642.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1375+479_1375+486d others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | ||||||
| chr11:33095819
|
C | CAAATAAA others(5): Show |
2 | a0001c0001t0001g0200a0001c0001t0001g0225 | 2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1375+475_1375+486d others(14): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | ||||||
| chr11:33095819
|
CAAATAAA others(5): Show |
C | 2 | a0001c0001t0001g0300a0001c0001t0001g0304 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1375+475_1375+486d others(14): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | ||||||
| chr11:33095823
|
T | A | 176 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(173): Show | 199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1375+483A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095823 | ||||||
| chr11:33095827
|
T | A | 78 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0018others(75): Show | 82 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1375+479A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095827 | ||||||
| chr11:33095831
|
T | A | 23 | a0001c0001t0002g0029a0001c0001t0002g0031a0001c0001t0002g0033others(20): Show | 24 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1375+475A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095831 | ||||||
| chr11:33095835
|
T | A | 7 | a0001c0001t0002g0029a0001c0001t0002g0056a0001c0001t0002g0079others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375+471A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095835 | ||||||
| chr11:33095844
|
A | G | 1 | a0001c0001t0003g0132 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1375+462T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095844 | ||||||
| chr11:33095863
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1375+443T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095863 | ||||||
| chr11:33095964
|
T | TTTTG | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1375+338_1375+341d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095964 | ||||||
| chr11:33096436
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1273-28A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096436 | ||||||
| chr11:33096441
|
A | G | 1 | a0001c0001t0003g0125 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1273-33T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096441 | ||||||
| chr11:33096530
|
A | G | 3 | a0001c0001t0002g0012a0001c0001t0002g0044a0001c0001t0002g0076 | 4 | NA18965.hp2 NA18966.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273-122T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096530 | ||||||
| chr11:33096591
|
G | T | 233 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0195others(230): Show | 257 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.1273-183C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096591 | ||||||
| chr11:33096728
|
A | G | 81 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0007others(78): Show | 96 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1272+107T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096728 | ||||||
| chr11:33096983
|
GC | G | 92 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0106others(89): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
splice_region_variant&intron_variant | LOW | c.1129-6delG | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33096983 | ||||||
| chr11:33097098
|
C | G | 1 | a0001c0001t0003g0121 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1129-120G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097098 | ||||||
| chr11:33097146
|
A | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0311a0001c0001t0001g0312others(2): Show | 6 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129-168T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097146 | ||||||
| chr11:33097152
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1129-174A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097152 | ||||||
| chr11:33097271
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1129-293A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097271 | ||||||
| chr11:33097342
|
G | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1129-364C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097342 | ||||||
| chr11:33097362
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1129-384C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097362 | ||||||
| chr11:33097376
|
G | GT | 6 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(3): Show | 6 | HG02717.hp2 HG03041.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-399dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097376 | ||||||
| chr11:33097416
|
C | G | 2 | a0001c0001t0002g0054a0001c0001t0002g0061 | 2 | NA18978.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1129-438G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097416 | ||||||
| chr11:33097453
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1129-475A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097453 | ||||||
| chr11:33097558
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1129-580C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097558 | ||||||
| chr11:33097580
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1129-602C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097580 | ||||||
| chr11:33097659
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1129-681C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097659 | ||||||
| chr11:33097731
|
G | A | 321 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(318): Show | 357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.1129-753C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097731 | ||||||
| chr11:33097794
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0030a0001c0001t0002g0090 | 3 | NA18946.hp1 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1129-816C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097794 | ||||||
| chr11:33098044
|
T | G | 8 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0112others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1128+646A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098044 | ||||||
| chr11:33098090
|
T | G | 1 | a0001c0001t0002g0043 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1128+600A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098090 | ||||||
| chr11:33098241
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1128+449C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098241 | ||||||
| chr11:33098264
|
T | G | 1 | a0001c0001t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1128+426A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098264 | ||||||
| chr11:33098468
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1128+222C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098468 | ||||||
| chr11:33098492
|
G | T | 1 | a0001c0001t0001g0200 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1128+198C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098492 | ||||||
| chr11:33099298
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.937-148G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 11/20 | chr11 | 33099298 | ||||||
| chr11:33100036
|
C | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.827-319G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100036 | ||||||
| chr11:33100059
|
T | C | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.827-342A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100059 | ||||||
| chr11:33100123
|
A | G | 181 | a0001c0001t0001g0318a0001c0001t0002g0005a0001c0001t0002g0006others(178): Show | 204 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.827-406T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100123 | ||||||
| chr11:33100166
|
C | T | 1 | a0001c0002t0002g0008 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.827-449G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100166 | ||||||
| chr11:33100280
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.827-563C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100280 | ||||||
| chr11:33100354
|
C | CA | 172 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(169): Show | 194 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.827-638dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100354 | ||||||
| chr11:33100354
|
C | CAA | 7 | a0001c0001t0002g0018a0001c0001t0002g0070a0001c0001t0002g0078others(4): Show | 8 | HG01346.hp2 HG01496.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-639_827-638dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100354 | ||||||
| chr11:33100354
|
CA | C | 39 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(36): Show | 39 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.827-638delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100354 | ||||||
| chr11:33100860
|
T | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.827-1143A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100860 | ||||||
| chr11:33101421
|
G | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.826+756C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101421 | ||||||
| chr11:33101590
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.826+587C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101590 | ||||||
| chr11:33101632
|
A | T | 1 | a0001c0001t0002g0037 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.826+545T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101632 | ||||||
| chr11:33101636
|
C | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.826+541G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101636 | ||||||
| chr11:33101792
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.826+385A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101792 | ||||||
| chr11:33102348
|
C | G | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.664-9G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102348 | ||||||
| chr11:33102396
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.664-57G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102396 | ||||||
| chr11:33102522
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.664-183G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102522 | ||||||
| chr11:33102523
|
A | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.664-184T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102523 | ||||||
| chr11:33102902
|
A | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.663+205T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102902 | ||||||
| chr11:33102911
|
T | C | 3 | a0001c0001t0003g0148a0001c0001t0003g0179a0001c0001t0003g0187 | 3 | HG01346.hp2 NA18966.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.663+196A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102911 | ||||||
| chr11:33103216
|
G | T | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | NA18954.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.586-32C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103216 | ||||||
| chr11:33103500
|
G | A | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.586-316C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103500 | ||||||
| chr11:33103643
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.586-459C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103643 | ||||||
| chr11:33103669
|
T | C | 227 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(224): Show | 250 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.586-485A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103669 | ||||||
| chr11:33103757
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.586-573C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103757 | ||||||
| chr11:33104424
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.585+1143T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104424 | ||||||
| chr11:33104441
|
A | G | 1 | a0001c0001t0002g0076 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.585+1126T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104441 | ||||||
| chr11:33104458
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.585+1109G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104458 | ||||||
| chr11:33104538
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0296 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.585+1029C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104538 | ||||||
| chr11:33104543
|
G | A | 4 | a0001c0001t0003g0028a0001c0001t0003g0123a0001c0001t0003g0131others(1): Show | 4 | HG02080.hp1 NA18939.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+1024C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104543 | ||||||
| chr11:33104697
|
T | A | 1 | a0001c0001t0002g0044 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.585+870A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104697 | ||||||
| chr11:33104858
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.585+709C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104858 | ||||||
| chr11:33104878
|
T | C | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.585+689A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104878 | ||||||
| chr11:33104937
|
C | T | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.585+630G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104937 | ||||||
| chr11:33105272
|
C | A | 1 | a0001c0001t0001g0269 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.585+295G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33105272 | ||||||
| chr11:33105364
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.585+203T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33105364 | ||||||
| chr11:33106652
|
A | G | 2 | a0001c0001t0002g0162a0001c0001t0002g0173 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.357-588T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33106652 | ||||||
| chr11:33106710
|
G | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.357-646C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33106710 | ||||||
| chr11:33106778
|
CTTTATAT others(3): Show |
C | 1 | a0001c0001t0001g0317 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.357-724_357-715del others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33106778 | ||||||
| chr11:33107183
|
G | T | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.356+720C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33107183 | ||||||
| chr11:33107206
|
A | T | 1 | a0001c0001t0002g0060 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.356+697T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33107206 | ||||||
| chr11:33107296
|
C | T | 81 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0007others(78): Show | 96 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.356+607G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33107296 | ||||||
| chr11:33107634
|
G | GACA | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.356+266_356+268dup others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33107634 | ||||||
| chr11:33108199
|
C | T | 2 | a0001c0002t0002g0008a0001c0002t0002g0118 | 4 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+187G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 4/20 | chr11 | 33108199 | ||||||
| chr11:33108451
|
C | T | 80 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0007others(77): Show | 95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.226-33G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33108451 | ||||||
| chr11:33108986
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.226-568C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33108986 | ||||||
| chr11:33109251
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.226-833G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109251 | ||||||
| chr11:33109342
|
G | C | 1 | a0001c0001t0003g0142 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.226-924C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109342 | ||||||
| chr11:33109495
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0222 | 2 | HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.226-1077C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109495 | ||||||
| chr11:33109592
|
G | C | 1 | a0001c0001t0003g0122 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.226-1174C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109592 | ||||||
| chr11:33109607
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.226-1189T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109607 | ||||||
| chr11:33109666
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-1248A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109666 | ||||||
| chr11:33109685
|
C | T | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0079others(1): Show | 4 | NA18945.hp1 NA18955.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-1267G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109685 | ||||||
| chr11:33109754
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-1336T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109754 | ||||||
| chr11:33110004
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(1): Show | 4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-1586C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110004 | ||||||
| chr11:33110152
|
G | C | 1 | a0001c0001t0002g0073 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.226-1734C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110152 | ||||||
| chr11:33110461
|
T | C | 2 | a0001c0001t0001g0285a0001c0001t0001g0310 | 2 | HG01167.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.226-2043A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110461 | ||||||
| chr11:33110505
|
G | A | 1 | a0001c0001t0003g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.226-2087C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110505 | ||||||
| chr11:33110554
|
T | A | 1 | a0001c0001t0001g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.226-2136A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110554 | ||||||
| chr11:33110648
|
T | G | 1 | a0001c0001t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.226-2230A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110648 | ||||||
| chr11:33110751
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.226-2333T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110751 | ||||||
| chr11:33110881
|
T | TA | 11 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0235others(8): Show | 15 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-2464dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110881 | ||||||
| chr11:33110953
|
G | A | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-2535C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110953 | ||||||
| chr11:33111004
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(1): Show | 4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-2586C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111004 | ||||||
| chr11:33111138
|
G | A | 2 | a0001c0001t0003g0149a0001c0001t0003g0150 | 2 | HG00408.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.226-2720C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111138 | ||||||
| chr11:33111285
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-2867C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111285 | ||||||
| chr11:33111292
|
T | G | 1 | a0001c0001t0001g0274 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.226-2874A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111292 | ||||||
| chr11:33111318
|
T | C | 93 | a0001c0001t0001g0271a0001c0001t0002g0006a0001c0001t0002g0103others(90): Show | 111 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.226-2900A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111318 | ||||||
| chr11:33111366
|
G | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG02258.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.226-2948C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111366 | ||||||
| chr11:33111755
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0308 | 2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.226-3337A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111755 | ||||||
| chr11:33111975
|
C | A | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-3557G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111975 | ||||||
| chr11:33112011
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-3593A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112011 | ||||||
| chr11:33112083
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.226-3665C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112083 | ||||||
| chr11:33112255
|
G | GA | 7 | a0001c0001t0001g0196a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 7 | HG02027.hp2 HG02258.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-3838dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112255 | ||||||
| chr11:33112376
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.226-3958A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112376 | ||||||
| chr11:33112502
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.226-4084A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112502 | ||||||
| chr11:33112704
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226-4286C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112704 | ||||||
| chr11:33112713
|
A | C | 1 | a0001c0001t0002g0023 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.226-4295T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112713 | ||||||
| chr11:33112733
|
A | G | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226-4315T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112733 | ||||||
| chr11:33112928
|
A | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-4510T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112928 | ||||||
| chr11:33112942
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-4524A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112942 | ||||||
| chr11:33112970
|
G | A | 1 | a0001c0001t0003g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.226-4552C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112970 | ||||||
| chr11:33113000
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0315 | 3 | HG00735.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.226-4582C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113000 | ||||||
| chr11:33113076
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-4658C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113076 | ||||||
| chr11:33113176
|
A | G | 13 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(10): Show | 13 | HG02027.hp1 HG02040.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.226-4758T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113176 | ||||||
| chr11:33113206
|
A | AAAAT | 38 | a0001c0001t0001g0020a0001c0001t0001g0194a0001c0001t0001g0195others(35): Show | 42 | HG00642.hp2 HG00673.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.226-4792_226-4789d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | ||||||
| chr11:33113206
|
A | AAAATAAA others(1): Show |
5 | a0001c0001t0001g0199a0001c0001t0001g0273a0001c0001t0001g0319others(2): Show | 5 | HG02717.hp2 HG03041.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-4796_226-4789d others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | ||||||
| chr11:33113206
|
A | AAAATAAA others(5): Show |
4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0318others(1): Show | 4 | HG02647.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-4800_226-4789d others(14): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | ||||||
| chr11:33113206
|
AAAAT | A | 84 | a0001c0001t0002g0040a0001c0001t0002g0059a0001c0001t0002g0103others(81): Show | 99 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.226-4792_226-4789d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | ||||||
| chr11:33113206
|
AAAATAAA others(1): Show |
A | 85 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0002g0005others(82): Show | 89 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.226-4796_226-4789d others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | ||||||
| chr11:33113247
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.226-4829C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113247 | ||||||
| chr11:33113388
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.226-4970A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113388 | ||||||
| chr11:33113399
|
C | T | 7 | a0001c0001t0002g0013a0001c0001t0002g0035a0001c0001t0002g0043others(4): Show | 8 | NA18964.hp1 NA18970.hp2 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.226-4981G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113399 | ||||||
| chr11:33113453
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0173 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.226-5035G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113453 | ||||||
| chr11:33113511
|
T | C | 3 | a0001c0001t0001g0258a0001c0001t0001g0296a0001c0001t0001g0317 | 3 | HG02809.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.226-5093A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113511 | ||||||
| chr11:33113561
|
C | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0200a0001c0001t0001g0212others(1): Show | 4 | HG02896.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-5143G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113561 | ||||||
| chr11:33113774
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.226-5356C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113774 | ||||||
| chr11:33113995
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0316 | 2 | HG01069.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.226-5577G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113995 | ||||||
| chr11:33114367
|
T | C | 2 | a0001c0001t0002g0073a0001c0001t0002g0078 | 2 | NA18972.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.226-5949A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114367 | ||||||
| chr11:33114458
|
G | GA | 83 | a0001c0001t0002g0041a0001c0001t0002g0087a0001c0001t0002g0090others(80): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.226-6041dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114458 | ||||||
| chr11:33114463
|
A | AAAAATCC others(4): Show |
1 | a0001c0001t0002g0110 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.226-6046_226-6045i others(13): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114463 | ||||||
| chr11:33114521
|
T | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG00280.hp1 HG00733.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.226-6103A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114521 | ||||||
| chr11:33114570
|
G | T | 1 | a0001c0001t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.226-6152C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114570 | ||||||
| chr11:33114621
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-6203G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114621 | ||||||
| chr11:33114788
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-6370T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114788 | ||||||
| chr11:33114788
|
A | T | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(175): Show | 200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.226-6370T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114788 | ||||||
| chr11:33114891
|
T | C | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-6473A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114891 | ||||||
| chr11:33114945
|
C | A | 1 | a0001c0001t0001g0278 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.226-6527G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114945 | ||||||
| chr11:33115012
|
G | A | 4 | a0001c0001t0003g0028a0001c0001t0003g0123a0001c0001t0003g0131others(1): Show | 4 | HG02080.hp1 NA18939.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-6594C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115012 | ||||||
| chr11:33115085
|
C | T | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-6667G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115085 | ||||||
| chr11:33115115
|
C | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-6697G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115115 | ||||||
| chr11:33115233
|
A | C | 1 | a0001c0001t0001g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.226-6815T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115233 | ||||||
| chr11:33115237
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0242 | 2 | NA18946.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.226-6819A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115237 | ||||||
| chr11:33115470
|
T | C | 1 | a0001c0001t0003g0143 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.226-7052A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115470 | ||||||
| chr11:33115587
|
GTGACAAA others(4): Show |
G | 235 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0195others(232): Show | 259 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.226-7180_226-7170d others(13): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115587 | ||||||
| chr11:33115599
|
T | G | 235 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0195others(232): Show | 259 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.226-7181A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115599 | ||||||
| chr11:33115600
|
A | C | 235 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0195others(232): Show | 259 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.226-7182T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115600 | ||||||
| chr11:33115691
|
C | A | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.226-7273G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115691 | ||||||
| chr11:33116133
|
T | A | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.226-7715A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116133 | ||||||
| chr11:33116754
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.226-8336C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116754 | ||||||
| chr11:33116814
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.226-8396C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116814 | ||||||
| chr11:33116874
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-8456A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116874 | ||||||
| chr11:33116920
|
C | CT | 8 | a0001c0001t0002g0039a0001c0001t0002g0063a0001c0001t0002g0069others(5): Show | 8 | HG00597.hp1 HG00733.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-8503dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116920 | ||||||
| chr11:33117635
|
A | T | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-9217T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117635 | ||||||
| chr11:33117662
|
A | AAT | 216 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(213): Show | 238 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.226-9246_226-9245d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117662 | ||||||
| chr11:33117662
|
A | AATAT | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-9248_226-9245d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117662 | ||||||
| chr11:33117722
|
T | C | 3 | a0001c0001t0001g0258a0001c0001t0001g0296a0001c0001t0001g0317 | 3 | HG02809.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.226-9304A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117722 | ||||||
| chr11:33117804
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.226-9386G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117804 | ||||||
| chr11:33117873
|
G | A | 218 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(215): Show | 241 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.226-9455C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117873 | ||||||
| chr11:33117884
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.226-9466G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117884 | ||||||
| chr11:33118081
|
AT | A | 17 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0203others(14): Show | 18 | HG01069.hp1 HG01243.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.226-9664delA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118081 | ||||||
| chr11:33118099
|
T | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-9681A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118099 | ||||||
| chr11:33118474
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.226-10056A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118474 | ||||||
| chr11:33118476
|
G | T | 215 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(212): Show | 238 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.226-10058C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118476 | ||||||
| chr11:33118587
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0271 | 3 | HG01515.hp2 HG02683.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.226-10169T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118587 | ||||||
| chr11:33118625
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.226-10207A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118625 | ||||||
| chr11:33118683
|
A | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-10265T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118683 | ||||||
| chr11:33118747
|
TA | T | 176 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(173): Show | 199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.226-10330delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118747 | ||||||
| chr11:33118760
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.226-10342G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118760 | ||||||
| chr11:33119058
|
C | CT | 85 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(82): Show | 89 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.226-10641dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33119058 | ||||||
| chr11:33119120
|
T | G | 1 | a0001c0001t0003g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.226-10702A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33119120 | ||||||
| chr11:33119472
|
A | AT | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-11055dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33119472 | ||||||
| chr11:33119474
|
C | A | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-11056G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33119474 | ||||||
| chr11:33120136
|
T | G | 1 | a0001c0001t0001g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-11718A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120136 | ||||||
| chr11:33120328
|
G | C | 1 | a0001c0001t0001g0276 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11910C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120328 | ||||||
| chr11:33120330
|
G | T | 1 | a0001c0001t0001g0276 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11912C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120330 | ||||||
| chr11:33120332
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11914A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120332 | ||||||
| chr11:33120333
|
T | A | 1 | a0001c0001t0001g0276 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11915A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120333 | ||||||
| chr11:33120334
|
A | T | 1 | a0001c0001t0001g0276 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11916T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120334 | ||||||
| chr11:33120338
|
T | G | 1 | a0001c0001t0001g0276 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11920A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120338 | ||||||
| chr11:33120509
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-12091G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120509 | ||||||
| chr11:33120649
|
A | T | 1 | a0001c0001t0001g0250 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.226-12231T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120649 | ||||||
| chr11:33120815
|
T | C | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-12397A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120815 | ||||||
| chr11:33120893
|
A | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-12475T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120893 | ||||||
| chr11:33120895
|
T | C | 218 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(215): Show | 241 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.226-12477A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120895 | ||||||
| chr11:33121028
|
G | T | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-12610C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121028 | ||||||
| chr11:33121031
|
C | T | 1 | a0001c0001t0003g0145 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.226-12613G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121031 | ||||||
| chr11:33121076
|
C | G | 4 | a0001c0001t0002g0048a0001c0001t0002g0083a0001c0001t0002g0084others(1): Show | 4 | HG02040.hp1 HG02132.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-12658G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121076 | ||||||
| chr11:33121155
|
T | G | 2 | a0001c0001t0002g0073a0001c0001t0002g0078 | 2 | NA18972.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.226-12737A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121155 | ||||||
| chr11:33121252
|
C | T | 1 | a0001c0001t0002g0058 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.226-12834G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121252 | ||||||
| chr11:33121559
|
G | A | 1 | a0001c0001t0003g0126 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.226-13141C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121559 | ||||||
| chr11:33121580
|
G | A | 235 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0195others(232): Show | 259 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.226-13162C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121580 | ||||||
| chr11:33122175
|
A | T | 1 | a0001c0001t0002g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.226-13757T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122175 | ||||||
| chr11:33122441
|
T | C | 13 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(10): Show | 13 | HG02027.hp1 HG02040.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.226-14023A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122441 | ||||||
| chr11:33122671
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226-14253A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122671 | ||||||
| chr11:33122785
|
A | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-14367T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122785 | ||||||
| chr11:33122864
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.226-14446G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122864 | ||||||
| chr11:33122914
|
C | CA | 15 | a0001c0001t0001g0209a0001c0001t0001g0222a0001c0001t0001g0228others(12): Show | 15 | HG00438.hp1 HG00544.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-14497dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122914 | ||||||
| chr11:33122914
|
CA | C | 84 | a0001c0001t0001g0212a0001c0001t0001g0274a0001c0001t0002g0005others(81): Show | 94 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.226-14497delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122914 | ||||||
| chr11:33122914
|
CAA | C | 88 | a0001c0001t0002g0006a0001c0001t0002g0040a0001c0001t0002g0049others(85): Show | 100 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.226-14498_226-1449 others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122914 | ||||||
| chr11:33122930
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.226-14512T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122930 | ||||||
| chr11:33122931
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.226-14513T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122931 | ||||||
| chr11:33123029
|
A | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0074 | 2 | HG00438.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.226-14611T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123029 | ||||||
| chr11:33123150
|
T | C | 1 | a0001c0001t0004g0191 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.226-14732A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123150 | ||||||
| chr11:33123640
|
C | T | 5 | a0001c0001t0002g0027a0001c0001t0002g0030a0001c0001t0002g0075others(2): Show | 5 | HG00423.hp2 NA18946.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-15222G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123640 | ||||||
| chr11:33123692
|
T | TA | 10 | a0001c0001t0001g0275a0001c0001t0002g0023a0001c0001t0002g0029others(7): Show | 10 | HG00741.hp1 HG01109.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.226-15275dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123692 | ||||||
| chr11:33123723
|
A | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-15305T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123723 | ||||||
| chr11:33123850
|
T | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-15432A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123850 | ||||||
| chr11:33124081
|
C | A | 1 | a0001c0001t0001g0314 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.226-15663G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124081 | ||||||
| chr11:33124082
|
A | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-15664T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124082 | ||||||
| chr11:33124139
|
T | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0074 | 3 | HG00438.hp2 HG02015.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.226-15721A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124139 | ||||||
| chr11:33124194
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.226-15776T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124194 | ||||||
| chr11:33124231
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0007g0193 | 2 | HG01433.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.226-15813T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124231 | ||||||
| chr11:33124351
|
C | G | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226-15933G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124351 | ||||||
| chr11:33124474
|
C | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-16056G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124474 | ||||||
| chr11:33124593
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-16175C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124593 | ||||||
| chr11:33124698
|
T | G | 81 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0007others(78): Show | 96 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.226-16280A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124698 | ||||||
| chr11:33124868
|
C | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.226-16450G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124868 | ||||||
| chr11:33125080
|
C | G | 4 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(1): Show | 4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+16587G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125080 | ||||||
| chr11:33125387
|
ACT | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0030a0001c0001t0002g0090 | 3 | NA18946.hp1 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.225+16278_225+1627 others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125387 | ||||||
| chr11:33125556
|
C | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+16111G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125556 | ||||||
| chr11:33125705
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.225+15962A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125705 | ||||||
| chr11:33125717
|
C | T | 1 | a0001c0001t0004g0190 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.225+15950G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125717 | ||||||
| chr11:33125755
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+15912C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125755 | ||||||
| chr11:33125848
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.225+15819C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125848 | ||||||
| chr11:33126018
|
C | T | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.225+15649G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126018 | ||||||
| chr11:33126061
|
A | G | 3 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0317 | 3 | HG02647.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.225+15606T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126061 | ||||||
| chr11:33126182
|
A | G | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+15485T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126182 | ||||||
| chr11:33126249
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0242 | 2 | NA18946.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.225+15418G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126249 | ||||||
| chr11:33126303
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+15364G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126303 | ||||||
| chr11:33126398
|
G | A | 10 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0112others(7): Show | 11 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.225+15269C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126398 | ||||||
| chr11:33126407
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.225+15260C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126407 | ||||||
| chr11:33126409
|
G | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+15258C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126409 | ||||||
| chr11:33126413
|
G | A | 1 | a0001c0001t0003g0126 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.225+15254C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126413 | ||||||
| chr11:33126425
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.225+15242C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126425 | ||||||
| chr11:33126480
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.225+15187A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126480 | ||||||
| chr11:33126825
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+14842A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126825 | ||||||
| chr11:33127012
|
T | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+14655A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127012 | ||||||
| chr11:33127025
|
A | C | 2 | a0001c0001t0003g0144a0001c0001t0003g0180 | 2 | HG01175.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.225+14642T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127025 | ||||||
| chr11:33127148
|
T | G | 321 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(318): Show | 357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.225+14519A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127148 | ||||||
| chr11:33127187
|
A | T | 31 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(28): Show | 31 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.225+14480T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127187 | ||||||
| chr11:33127229
|
T | A | 1 | a0001c0001t0002g0090 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.225+14438A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127229 | ||||||
| chr11:33127301
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0030a0001c0001t0002g0090 | 3 | NA18946.hp1 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.225+14366T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127301 | ||||||
| chr11:33127639
|
T | C | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(175): Show | 200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.225+14028A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127639 | ||||||
| chr11:33127742
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0273a0001c0001t0001g0298others(2): Show | 7 | NA18955.hp2 NA18960.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+13925C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127742 | ||||||
| chr11:33127786
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0311a0001c0001t0001g0312others(2): Show | 6 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+13881G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127786 | ||||||
| chr11:33128001
|
T | C | 1 | a0001c0001t0003g0116 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.225+13666A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128001 | ||||||
| chr11:33128076
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+13591C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128076 | ||||||
| chr11:33128201
|
A | C | 1 | a0001c0001t0002g0018 | 2 | HG01496.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.225+13466T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128201 | ||||||
| chr11:33128412
|
T | C | 1 | a0001c0001t0003g0168 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.225+13255A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128412 | ||||||
| chr11:33128707
|
T | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+12960A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128707 | ||||||
| chr11:33128849
|
C | T | 4 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0154others(1): Show | 4 | NA18957.hp2 NA18962.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+12818G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128849 | ||||||
| chr11:33129012
|
T | C | 1 | a0001c0001t0003g0116 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.225+12655A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129012 | ||||||
| chr11:33129057
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.225+12610C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129057 | ||||||
| chr11:33129138
|
C | T | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(175): Show | 200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.225+12529G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129138 | ||||||
| chr11:33129192
|
A | G | 1 | a0001c0001t0002g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.225+12475T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129192 | ||||||
| chr11:33129376
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+12291C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129376 | ||||||
| chr11:33129394
|
C | CT | 11 | a0001c0001t0001g0222a0001c0001t0001g0269a0001c0001t0001g0273others(8): Show | 11 | HG01099.hp2 HG01943.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.225+12272dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129394 | ||||||
| chr11:33129394
|
C | CTT | 7 | a0001c0001t0001g0196a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 7 | HG02258.hp2 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+12271_225+1227 others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129394 | ||||||
| chr11:33129655
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.225+12012T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129655 | ||||||
| chr11:33129958
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.225+11709C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129958 | ||||||
| chr11:33130108
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.225+11559C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33130108 | ||||||
| chr11:33130243
|
C | T | 1 | a0001c0001t0004g0191 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.225+11424G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33130243 | ||||||
| chr11:33130528
|
T | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+11139A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33130528 | ||||||
| chr11:33130657
|
A | T | 1 | a0001c0001t0002g0109 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.225+11010T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33130657 | ||||||
| chr11:33131359
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.225+10308G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131359 | ||||||
| chr11:33131429
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+10238G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131429 | ||||||
| chr11:33131472
|
T | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0311a0001c0001t0001g0312others(3): Show | 7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+10195A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131472 | ||||||
| chr11:33131480
|
G | A | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.225+10187C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131480 | ||||||
| chr11:33131575
|
G | A | 3 | a0001c0001t0001g0309a0001c0001t0002g0018a0001c0001t0002g0189 | 4 | HG01496.hp1 HG02486.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+10092C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131575 | ||||||
| chr11:33131584
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.225+10083G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131584 | ||||||
| chr11:33131597
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.225+10070G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131597 | ||||||
| chr11:33131613
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225+10054C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131613 | ||||||
| chr11:33131628
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.225+10039G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131628 | ||||||
| chr11:33131639
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+10028C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131639 | ||||||
| chr11:33131690
|
C | CA | 98 | a0001c0001t0001g0003a0001c0001t0001g0235a0001c0001t0001g0236others(95): Show | 106 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.225+9976dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131690 | ||||||
| chr11:33131713
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.225+9954C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131713 | ||||||
| chr11:33131745
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0307 | 2 | HG00597.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.225+9922C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131745 | ||||||
| chr11:33131760
|
G | A | 8 | a0001c0001t0002g0034a0001c0001t0002g0039a0001c0001t0002g0041others(5): Show | 8 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+9907C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131760 | ||||||
| chr11:33131768
|
C | T | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(175): Show | 200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.225+9899G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131768 | ||||||
| chr11:33131812
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.225+9855T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131812 | ||||||
| chr11:33131898
|
ATTGTGGT others(18): Show |
A | 4 | a0001c0001t0001g0194a0001c0001t0001g0200a0001c0001t0001g0212others(1): Show | 4 | HG02896.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+9744_225+9768d others(27): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131898 | ||||||
| chr11:33131995
|
G | A | 8 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0112others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+9672C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131995 | ||||||
| chr11:33132077
|
C | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+9590G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132077 | ||||||
| chr11:33132238
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+9429T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132238 | ||||||
| chr11:33132463
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+9204C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132463 | ||||||
| chr11:33132633
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.225+9034T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132633 | ||||||
| chr11:33132634
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.225+9033G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132634 | ||||||
| chr11:33132635
|
C | A | 1 | a0001c0001t0001g0233 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.225+9032G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132635 | ||||||
| chr11:33132657
|
G | A | 4 | a0001c0001t0001g0216a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG02965.hp2 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+9010C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132657 | ||||||
| chr11:33132831
|
G | A | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(175): Show | 200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.225+8836C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132831 | ||||||
| chr11:33132850
|
A | T | 1 | a0001c0001t0003g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.225+8817T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132850 | ||||||
| chr11:33132943
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.225+8724A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132943 | ||||||
| chr11:33133110
|
CT | C | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+8556delA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133110 | ||||||
| chr11:33133132
|
G | A | 81 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0007others(78): Show | 96 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.225+8535C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133132 | ||||||
| chr11:33133282
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+8385A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133282 | ||||||
| chr11:33133345
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0173 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.225+8322G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133345 | ||||||
| chr11:33133577
|
C | T | 1 | a0001c0001t0003g0116 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.225+8090G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133577 | ||||||
| chr11:33133718
|
A | G | 84 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(81): Show | 88 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.225+7949T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133718 | ||||||
| chr11:33133759
|
G | A | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.225+7908C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133759 | ||||||
| chr11:33133833
|
T | C | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+7834A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133833 | ||||||
| chr11:33134051
|
A | G | 3 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0304 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.225+7616T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134051 | ||||||
| chr11:33134268
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0030a0001c0001t0002g0090 | 3 | NA18946.hp1 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.225+7399C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134268 | ||||||
| chr11:33134416
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.225+7251T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134416 | ||||||
| chr11:33134586
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225+7081A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134586 | ||||||
| chr11:33134676
|
AC | A | 92 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0106others(89): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.225+6990delG | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134676 | ||||||
| chr11:33134706
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225+6961G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134706 | ||||||
| chr11:33134719
|
T | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0296 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.225+6948A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134719 | ||||||
| chr11:33134820
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+6847T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134820 | ||||||
| chr11:33134852
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0311a0001c0001t0001g0312others(3): Show | 7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+6815T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134852 | ||||||
| chr11:33135077
|
C | G | 2 | a0001c0001t0002g0162a0001c0001t0002g0173 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.225+6590G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135077 | ||||||
| chr11:33135185
|
T | TA | 4 | a0001c0001t0001g0251a0001c0001t0002g0080a0001c0001t0002g0130others(1): Show | 4 | HG02135.hp2 HG04115.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+6481dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135185 | ||||||
| chr11:33135408
|
C | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0316 | 2 | HG01069.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.225+6259G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135408 | ||||||
| chr11:33135678
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0291 | 2 | NA18980.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.225+5989A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135678 | ||||||
| chr11:33135755
|
CCTT | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+5909_225+5911d others(5): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135755 | ||||||
| chr11:33136288
|
C | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+5379G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136288 | ||||||
| chr11:33136590
|
T | C | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0079others(1): Show | 4 | NA18945.hp1 NA18955.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+5077A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136590 | ||||||
| chr11:33136596
|
T | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.225+5071A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136596 | ||||||
| chr11:33136612
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.225+5055A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136612 | ||||||
| chr11:33136687
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.225+4980A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136687 | ||||||
| chr11:33136908
|
T | C | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+4759A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136908 | ||||||
| chr11:33136915
|
C | CT | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+4751dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136915 | ||||||
| chr11:33137020
|
T | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.225+4647A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33137020 | ||||||
| chr11:33137115
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.225+4552C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33137115 | ||||||
| chr11:33137258
|
C | A | 1 | a0001c0001t0003g0183 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.225+4409G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33137258 | ||||||
| chr11:33137989
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.225+3678A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33137989 | ||||||
| chr11:33138128
|
G | C | 1 | a0001c0001t0002g0052 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.225+3539C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138128 | ||||||
| chr11:33138172
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+3495G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138172 | ||||||
| chr11:33138222
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+3445T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138222 | ||||||
| chr11:33138459
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.225+3208A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138459 | ||||||
| chr11:33138671
|
T | G | 1 | a0001c0001t0003g0188 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.225+2996A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138671 | ||||||
| chr11:33138830
|
T | A | 1 | a0001c0001t0002g0042 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.225+2837A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138830 | ||||||
| chr11:33138982
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.225+2685A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138982 | ||||||
| chr11:33139081
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.225+2586G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139081 | ||||||
| chr11:33139138
|
A | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0296 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.225+2529T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139138 | ||||||
| chr11:33139442
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.225+2225G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139442 | ||||||
| chr11:33139503
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.225+2164A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139503 | ||||||
| chr11:33139514
|
G | T | 1 | a0001c0001t0002g0074 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.225+2153C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139514 | ||||||
| chr11:33139744
|
G | A | 85 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(82): Show | 89 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.225+1923C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139744 | ||||||
| chr11:33139835
|
A | C | 1 | a0001c0001t0001g0248 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.225+1832T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139835 | ||||||
| chr11:33139915
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.225+1752A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139915 | ||||||
| chr11:33139955
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.225+1712C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139955 | ||||||
| chr11:33140463
|
A | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.225+1204T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33140463 | ||||||
| chr11:33140494
|
C | T | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.225+1173G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33140494 | ||||||
| chr11:33140850
|
A | AC | 6 | a0001c0001t0001g0021a0001c0001t0001g0311a0001c0001t0001g0312others(3): Show | 7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+816dupG | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33140850 | ||||||
| chr11:33140907
|
T | C | 5 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0083others(2): Show | 5 | HG02027.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+760A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33140907 | ||||||
| chr11:33141091
|
TGATTAAA others(3): Show |
T | 1 | a0001c0001t0001g0306 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.225+566_225+575del others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33141091 | ||||||
| chr11:33142219
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.28-233T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142219 | ||||||
| chr11:33142336
|
GAT | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-352_28-351delAT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142336 | ||||||
| chr11:33142384
|
C | A | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.28-398G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142384 | ||||||
| chr11:33142476
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.28-490A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142476 | ||||||
| chr11:33142510
|
T | A | 2 | a0001c0001t0002g0073a0001c0001t0002g0078 | 2 | NA18972.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.28-524A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142510 | ||||||
| chr11:33142571
|
A | G | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.28-585T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142571 | ||||||
| chr11:33142573
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-587T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142573 | ||||||
| chr11:33142603
|
A | G | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.28-617T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142603 | ||||||
| chr11:33142616
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.28-630C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142616 | ||||||
| chr11:33142729
|
CAT | C | 2 | a0001c0001t0001g0244a0001c0001t0002g0006 | 4 | HG02559.hp1 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-745_28-744delAT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142729 | ||||||
| chr11:33142909
|
C | G | 4 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(1): Show | 4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-923G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142909 | ||||||
| chr11:33142981
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-995A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142981 | ||||||
| chr11:33143037
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-1051C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143037 | ||||||
| chr11:33143072
|
T | C | 1 | a0001c0001t0003g0169 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.28-1086A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143072 | ||||||
| chr11:33143353
|
T | C | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0220 | 3 | HG02723.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.28-1367A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143353 | ||||||
| chr11:33143558
|
A | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-1572T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143558 | ||||||
| chr11:33143569
|
T | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-1583A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143569 | ||||||
| chr11:33143723
|
T | C | 4 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0219others(1): Show | 4 | HG02630.hp2 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1737A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143723 | ||||||
| chr11:33143863
|
G | A | 1 | a0001c0001t0004g0191 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.28-1877C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143863 | ||||||
| chr11:33143938
|
C | T | 31 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(28): Show | 31 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.28-1952G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143938 | ||||||
| chr11:33144120
|
C | T | 5 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157others(2): Show | 5 | HG02145.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-2134G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144120 | ||||||
| chr11:33144129
|
C | T | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.28-2143G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144129 | ||||||
| chr11:33144132
|
T | C | 1 | a0001c0001t0003g0151 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.28-2146A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144132 | ||||||
| chr11:33144137
|
TTTAGTGG others(2): Show |
T | 88 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(85): Show | 93 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.28-2160_28-2152del others(9): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144137 | ||||||
| chr11:33144138
|
TTAGTGGA others(1): Show |
T | 92 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0106others(89): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.28-2160_28-2153del others(8): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144138 | ||||||
| chr11:33144269
|
G | A | 7 | a0001c0001t0003g0017a0001c0001t0003g0144a0001c0001t0003g0145others(4): Show | 8 | HG00741.hp2 HG01099.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-2283C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144269 | ||||||
| chr11:33144402
|
G | A | 2 | a0001c0001t0002g0110a0001c0001t0002g0159 | 2 | NA18967.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.28-2416C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144402 | ||||||
| chr11:33144425
|
T | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-2439A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144425 | ||||||
| chr11:33144516
|
T | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-2530A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144516 | ||||||
| chr11:33144630
|
A | C | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.28-2644T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144630 | ||||||
| chr11:33144632
|
G | C | 1 | a0001c0001t0002g0051 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.28-2646C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144632 | ||||||
| chr11:33144684
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.28-2698T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144684 | ||||||
| chr11:33144685
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0020others(21): Show | 30 | HG00438.hp1 HG00673.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.28-2699C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144685 | ||||||
| chr11:33144694
|
T | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-2708A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144694 | ||||||
| chr11:33144749
|
G | C | 8 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0112others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-2763C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144749 | ||||||
| chr11:33144919
|
G | C | 1 | a0001c0001t0001g0288 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.28-2933C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144919 | ||||||
| chr11:33144924
|
T | C | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.28-2938A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144924 | ||||||
| chr11:33144977
|
TA | T | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.28-2992delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144977 | ||||||
| chr11:33145279
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.28-3293A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145279 | ||||||
| chr11:33145421
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.28-3435C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145421 | ||||||
| chr11:33145502
|
A | G | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-3516T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145502 | ||||||
| chr11:33145565
|
C | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0030 | 2 | NA18946.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.28-3579G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145565 | ||||||
| chr11:33145691
|
G | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0019others(37): Show | 49 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.28-3705C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145691 | ||||||
| chr11:33145827
|
A | C | 1 | a0001c0001t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-3841T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145827 | ||||||
| chr11:33145957
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.28-3971G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145957 | ||||||
| chr11:33146066
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0267 | 2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.28-4080G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146066 | ||||||
| chr11:33146088
|
A | C | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.28-4102T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146088 | ||||||
| chr11:33146238
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-4252C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146238 | ||||||
| chr11:33146252
|
G | GA | 10 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0112others(7): Show | 11 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-4267dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146252 | ||||||
| chr11:33146528
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.28-4542C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146528 | ||||||
| chr11:33146623
|
T | TA | 92 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0019others(89): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.28-4638dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146623 | ||||||
| chr11:33146623
|
T | TAA | 178 | a0001c0001t0001g0298a0001c0001t0002g0005a0001c0001t0002g0006others(175): Show | 201 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.28-4639_28-4638dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146623 | ||||||
| chr11:33146753
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0316 | 2 | HG01069.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.28-4767G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146753 | ||||||
| chr11:33146855
|
GA | G | 84 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(81): Show | 88 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.28-4870delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146855 | ||||||
| chr11:33147060
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.28-5074C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147060 | ||||||
| chr11:33147207
|
A | T | 1 | a0001c0001t0003g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.28-5221T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147207 | ||||||
| chr11:33147224
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.28-5238C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147224 | ||||||
| chr11:33147254
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-5268C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147254 | ||||||
| chr11:33147317
|
C | G | 1 | a0001c0002t0002g0008 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.28-5331G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147317 | ||||||
| chr11:33147348
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0311a0001c0001t0001g0312others(3): Show | 7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-5362C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147348 | ||||||
| chr11:33147412
|
T | C | 13 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(10): Show | 13 | HG02027.hp1 HG02040.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-5426A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147412 | ||||||
| chr11:33147486
|
T | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-5500A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147486 | ||||||
| chr11:33147520
|
A | G | 218 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(215): Show | 241 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.28-5534T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147520 | ||||||
| chr11:33147555
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-5569G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147555 | ||||||
| chr11:33147618
|
T | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.28-5632A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147618 | ||||||
| chr11:33147785
|
A | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-5799T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147785 | ||||||
| chr11:33147865
|
T | G | 1 | a0001c0001t0002g0044 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.28-5879A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147865 | ||||||
| chr11:33148097
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG01243.hp1 HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.28-6111G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148097 | ||||||
| chr11:33148141
|
C | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-6155G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148141 | ||||||
| chr11:33148186
|
A | G | 1 | a0001c0001t0003g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.28-6200T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148186 | ||||||
| chr11:33148192
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0311a0001c0001t0001g0312others(3): Show | 7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-6206G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148192 | ||||||
| chr11:33148434
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.28-6448G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148434 | ||||||
| chr11:33148466
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.28-6480C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148466 | ||||||
| chr11:33148534
|
T | TAAAAATA others(180): Show |
1 | a0001c0001t0001g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(187): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(181): Show |
1 | a0001c0001t0001g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(188): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(185): Show |
1 | a0001c0001t0001g0243 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(192): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(186): Show |
1 | a0001c0001t0001g0244 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(193): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(187): Show |
1 | a0001c0001t0001g0242 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(194): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(188): Show |
1 | a0001c0001t0001g0240 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(195): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(195): Show |
2 | a0001c0001t0001g0239a0001c0001t0001g0308 | 2 | HG00738.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.28-6549_28-6548ins others(202): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(196): Show |
1 | a0001c0001t0001g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(203): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(197): Show |
4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0291others(1): Show | 4 | HG01358.hp1 NA18939.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-6549_28-6548ins others(204): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(199): Show |
2 | a0001c0001t0001g0248a0001c0001t0001g0251 | 2 | HG04115.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.28-6549_28-6548ins others(206): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(200): Show |
2 | a0001c0001t0001g0233a0001c0001t0001g0241 | 2 | HG00323.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.28-6549_28-6548ins others(207): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(205): Show |
1 | a0001c0001t0001g0250 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(212): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(209): Show |
1 | a0001c0001t0001g0293 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(216): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148534
|
T | TAAAAATA others(204): Show |
1 | a0001c0001t0001g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(211): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | ||||||
| chr11:33148572
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-6586A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148572 | ||||||
| chr11:33148596
|
T | C | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051 | 3 | HG02080.hp2 HG02129.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.28-6610A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148596 | ||||||
| chr11:33148694
|
C | CA | 80 | a0001c0001t0001g0313a0001c0001t0002g0005a0001c0001t0002g0023others(77): Show | 83 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.28-6709dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148694 | ||||||
| chr11:33148694
|
C | CAA | 16 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0032others(13): Show | 18 | HG00438.hp2 HG01981.hp2 HG04204.hp2 others(15): Show |
intron_variant | MODIFIER | c.28-6710_28-6709dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148694 | ||||||
| chr11:33148825
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0242 | 2 | NA18946.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.28-6839G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148825 | ||||||
| chr11:33148837
|
A | G | 7 | a0001c0001t0001g0196a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 7 | HG02258.hp2 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-6851T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148837 | ||||||
| chr11:33148844
|
T | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0013others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.28-6858A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148844 | ||||||
| chr11:33148856
|
C | CTG | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.28-6872_28-6871dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148856 | ||||||
| chr11:33148860
|
G | GT | 141 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(138): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.28-6875dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148860 | ||||||
| chr11:33148860
|
G | GTT | 41 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0032others(38): Show | 45 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.28-6876_28-6875dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148860 | ||||||
| chr11:33148860
|
GT | G | 35 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(32): Show | 35 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-6875delA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148860 | ||||||
| chr11:33148866
|
T | G | 4 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(1): Show | 4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-6880A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148866 | ||||||
| chr11:33148915
|
A | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-6929T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148915 | ||||||
| chr11:33148971
|
C | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-6985G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148971 | ||||||
| chr11:33149307
|
A | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-7321T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33149307 | ||||||
| chr11:33149714
|
T | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0173 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28-7728A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33149714 | ||||||
| chr11:33149982
|
G | A | 1 | a0001c0001t0003g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.28-7996C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33149982 | ||||||
| chr11:33150033
|
C | A | 1 | a0001c0001t0003g0154 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.28-8047G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150033 | ||||||
| chr11:33150034
|
A | AAAC | 85 | a0001c0001t0002g0103a0001c0001t0002g0112a0001c0001t0002g0129others(82): Show | 101 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.28-8051_28-8049dup others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150034 | ||||||
| chr11:33150034
|
A | AAACAAC | 87 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0013others(84): Show | 92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.28-8054_28-8049dup others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150034 | ||||||
| chr11:33150034
|
A | AAACAACA others(2): Show |
3 | a0001c0001t0002g0012a0001c0001t0002g0044a0001c0001t0002g0076 | 4 | NA18965.hp2 NA18966.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-8057_28-8049dup others(9): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150034 | ||||||
| chr11:33150034
|
A | C | 1 | a0001c0001t0003g0154 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.28-8048T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150034 | ||||||
| chr11:33150122
|
G | A | 5 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157others(2): Show | 5 | HG02145.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-8136C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150122 | ||||||
| chr11:33150153
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.28-8167A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150153 | ||||||
| chr11:33150196
|
C | G | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.28-8210G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150196 | ||||||
| chr11:33150219
|
T | TA | 44 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(41): Show | 44 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.28-8234dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150219 | ||||||
| chr11:33150219
|
TA | T | 170 | a0001c0001t0001g0238a0001c0001t0001g0255a0001c0001t0001g0284others(167): Show | 191 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.28-8234delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150219 | ||||||
| chr11:33150219
|
TAA | T | 8 | a0001c0001t0002g0043a0001c0001t0002g0087a0001c0001t0002g0110others(5): Show | 8 | HG01256.hp2 HG02015.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-8235_28-8234del others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150219 | ||||||
| chr11:33150250
|
G | GAA | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.28-8266_28-8265dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150250 | ||||||
| chr11:33150420
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28-8434G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150420 | ||||||
| chr11:33150673
|
T | C | 5 | a0001c0001t0002g0076a0001c0001t0003g0146a0001c0001t0003g0147others(2): Show | 5 | NA18957.hp2 NA18962.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-8687A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150673 | ||||||
| chr11:33150855
|
C | CA | 12 | a0001c0001t0001g0278a0001c0001t0001g0289a0001c0001t0001g0305others(9): Show | 13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-8870dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150855 | ||||||
| chr11:33151217
|
A | T | 1 | a0001c0001t0006g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.28-9231T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151217 | ||||||
| chr11:33151257
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.28-9271G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151257 | ||||||
| chr11:33151585
|
T | C | 1 | a0001c0001t0002g0079 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.28-9599A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151585 | ||||||
| chr11:33151601
|
C | T | 81 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0007others(78): Show | 96 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.28-9615G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151601 | ||||||
| chr11:33151611
|
T | C | 4 | a0001c0001t0001g0196a0001c0001t0001g0201a0001c0001t0001g0210others(1): Show | 4 | HG02258.hp2 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-9625A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151611 | ||||||
| chr11:33151707
|
T | C | 92 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0106others(89): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.27+9592A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151707 | ||||||
| chr11:33151735
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.27+9564C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151735 | ||||||
| chr11:33151807
|
T | C | 1 | a0001c0001t0001g0314 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.27+9492A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151807 | ||||||
| chr11:33152069
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+9230G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152069 | ||||||
| chr11:33152182
|
G | A | 1 | a0001c0001t0003g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.27+9117C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152182 | ||||||
| chr11:33152185
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27+9114C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152185 | ||||||
| chr11:33152269
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+9030C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152269 | ||||||
| chr11:33152294
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+9005C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152294 | ||||||
| chr11:33152317
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+8982A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152317 | ||||||
| chr11:33152327
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.27+8972G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152327 | ||||||
| chr11:33152362
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.27+8937G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152362 | ||||||
| chr11:33152433
|
T | G | 1 | a0001c0001t0001g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.27+8866A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152433 | ||||||
| chr11:33152471
|
T | A | 1 | a0001c0001t0001g0279 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27+8828A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152471 | ||||||
| chr11:33152498
|
C | T | 218 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(215): Show | 241 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.27+8801G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152498 | ||||||
| chr11:33152544
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+8755C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152544 | ||||||
| chr11:33152731
|
T | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+8568A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152731 | ||||||
| chr11:33152749
|
A | C | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.27+8550T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152749 | ||||||
| chr11:33152857
|
G | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+8442C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152857 | ||||||
| chr11:33152995
|
G | A | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+8304C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152995 | ||||||
| chr11:33152999
|
T | G | 1 | a0001c0001t0002g0086 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.27+8300A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152999 | ||||||
| chr11:33153018
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.27+8281C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153018 | ||||||
| chr11:33153182
|
A | G | 81 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0007others(78): Show | 96 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.27+8117T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153182 | ||||||
| chr11:33153298
|
A | G | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+8001T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153298 | ||||||
| chr11:33153384
|
C | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0322 | 3 | HG02717.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.27+7915G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153384 | ||||||
| chr11:33153449
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.27+7850C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153449 | ||||||
| chr11:33153512
|
A | C | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+7787T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153512 | ||||||
| chr11:33153629
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.27+7670A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153629 | ||||||
| chr11:33153643
|
A | C | 1 | a0001c0001t0002g0041 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.27+7656T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153643 | ||||||
| chr11:33153675
|
C | A | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+7624G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153675 | ||||||
| chr11:33153712
|
C | CA | 109 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0239others(106): Show | 127 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.27+7586dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153712 | ||||||
| chr11:33153712
|
C | CAA | 86 | a0001c0001t0001g0234a0001c0001t0001g0250a0001c0001t0001g0251others(83): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.27+7585_27+7586dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153712 | ||||||
| chr11:33153795
|
C | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+7504G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153795 | ||||||
| chr11:33153805
|
G | A | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(175): Show | 200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.27+7494C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153805 | ||||||
| chr11:33153871
|
C | T | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+7428G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153871 | ||||||
| chr11:33153939
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.27+7360G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153939 | ||||||
| chr11:33154107
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.27+7192G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154107 | ||||||
| chr11:33154212
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.27+7087C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154212 | ||||||
| chr11:33154240
|
T | C | 1 | a0001c0002t0002g0008 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.27+7059A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154240 | ||||||
| chr11:33154352
|
A | C | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+6947T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154352 | ||||||
| chr11:33154486
|
ACTTT | A | 156 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(153): Show | 178 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.27+6809_27+6812del others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154486 | ||||||
| chr11:33154487
|
CTTTCT | C | 7 | a0001c0001t0002g0081a0001c0001t0003g0028a0001c0001t0003g0131others(4): Show | 7 | HG00323.hp2 HG01256.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+6807_27+6811del others(5): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154487 | ||||||
| chr11:33154488
|
TTTC | T | 15 | a0001c0001t0002g0026a0001c0001t0002g0036a0001c0001t0002g0037others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.27+6808_27+6810del others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154488 | ||||||
| chr11:33154491
|
C | CT | 7 | a0001c0001t0001g0239a0001c0001t0001g0253a0001c0001t0001g0254others(4): Show | 7 | HG00099.hp2 HG02148.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+6807dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154491 | ||||||
| chr11:33154491
|
CT | C | 51 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0195others(48): Show | 52 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.27+6807delA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154491 | ||||||
| chr11:33154496
|
T | C | 35 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0197others(32): Show | 35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.27+6803A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154496 | ||||||
| chr11:33154497
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0230 | 2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.27+6802A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154497 | ||||||
| chr11:33154582
|
C | T | 1 | a0001c0001t0003g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.27+6717G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154582 | ||||||
| chr11:33154583
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.27+6716C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154583 | ||||||
| chr11:33154608
|
T | C | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(175): Show | 200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.27+6691A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154608 | ||||||
| chr11:33154699
|
A | G | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+6600T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154699 | ||||||
| chr11:33154943
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.27+6356G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154943 | ||||||
| chr11:33154976
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.27+6323G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154976 | ||||||
| chr11:33155018
|
T | C | 181 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(178): Show | 204 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.27+6281A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155018 | ||||||
| chr11:33155115
|
G | A | 38 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0107others(35): Show | 42 | HG00408.hp1 HG00741.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.27+6184C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155115 | ||||||
| chr11:33155128
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+6171C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155128 | ||||||
| chr11:33155217
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+6082C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155217 | ||||||
| chr11:33155249
|
C | A | 181 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(178): Show | 204 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.27+6050G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155249 | ||||||
| chr11:33155268
|
G | C | 1 | a0001c0001t0002g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.27+6031C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155268 | ||||||
| chr11:33155280
|
C | T | 8 | a0001c0001t0001g0258a0001c0001t0001g0296a0001c0001t0001g0317others(5): Show | 8 | HG02717.hp2 HG02809.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+6019G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155280 | ||||||
| chr11:33155283
|
G | C | 1 | a0001c0001t0001g0290 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.27+6016C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155283 | ||||||
| chr11:33155343
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.27+5956C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155343 | ||||||
| chr11:33155386
|
T | TA | 216 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0197others(213): Show | 239 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.27+5912dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155386 | ||||||
| chr11:33155386
|
TA | T | 7 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(4): Show | 7 | HG02723.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+5912delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155386 | ||||||
| chr11:33155542
|
T | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+5757A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155542 | ||||||
| chr11:33155543
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+5756G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155543 | ||||||
| chr11:33155846
|
G | A | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(175): Show | 200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.27+5453C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155846 | ||||||
| chr11:33155864
|
TA | T | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+5434delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155864 | ||||||
| chr11:33155971
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.27+5328G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155971 | ||||||
| chr11:33156289
|
CAT | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+5008_27+5009del others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156289 | ||||||
| chr11:33156320
|
C | G | 1 | a0001c0001t0002g0103 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+4979G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156320 | ||||||
| chr11:33156410
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.27+4889C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156410 | ||||||
| chr11:33156491
|
CATT | C | 9 | a0001c0001t0003g0002a0001c0001t0003g0107a0001c0001t0003g0149others(6): Show | 12 | HG00408.hp1 HG02015.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+4805_27+4807del others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156491 | ||||||
| chr11:33156792
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.27+4507G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156792 | ||||||
| chr11:33156955
|
A | G | 1 | a0001c0001t0003g0161 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.27+4344T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156955 | ||||||
| chr11:33157163
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.27+4136C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157163 | ||||||
| chr11:33157224
|
G | C | 1 | a0001c0001t0002g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.27+4075C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157224 | ||||||
| chr11:33157245
|
C | A | 1 | a0001c0001t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.27+4054G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157245 | ||||||
| chr11:33157304
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.27+3995C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157304 | ||||||
| chr11:33157322
|
T | G | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+3977A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157322 | ||||||
| chr11:33157323
|
C | G | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+3976G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157323 | ||||||
| chr11:33157324
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+3975G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157324 | ||||||
| chr11:33157325
|
A | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+3974T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157325 | ||||||
| chr11:33157776
|
A | T | 1 | a0001c0001t0002g0033 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27+3523T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157776 | ||||||
| chr11:33157890
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.27+3409A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157890 | ||||||
| chr11:33157913
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.27+3386T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157913 | ||||||
| chr11:33158223
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.27+3076T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158223 | ||||||
| chr11:33158285
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.27+3014G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158285 | ||||||
| chr11:33158475
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.27+2824T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158475 | ||||||
| chr11:33158596
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.27+2703C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158596 | ||||||
| chr11:33158602
|
C | A | 1 | a0001c0001t0003g0154 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.27+2697G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158602 | ||||||
| chr11:33158842
|
C | CAA | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+2455_27+2456dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158842 | ||||||
| chr11:33158927
|
TGAGACTA others(5): Show |
T | 1 | a0001c0001t0002g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.27+2360_27+2371del others(12): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158927 | ||||||
| chr11:33158960
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27+2339T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158960 | ||||||
| chr11:33158987
|
T | TA | 11 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0286others(8): Show | 11 | HG00280.hp2 HG00597.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+2311dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158987 | ||||||
| chr11:33158999
|
C | G | 1 | a0001c0001t0007g0193 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.27+2300G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158999 | ||||||
| chr11:33159104
|
ATT | A | 5 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157others(2): Show | 5 | HG02145.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2193_27+2194del others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159104 | ||||||
| chr11:33159180
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.27+2119C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159180 | ||||||
| chr11:33159312
|
T | C | 92 | a0001c0001t0002g0006a0001c0001t0002g0103a0001c0001t0002g0106others(89): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.27+1987A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159312 | ||||||
| chr11:33159353
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+1946A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159353 | ||||||
| chr11:33159530
|
A | G | 20 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(17): Show | 20 | HG00323.hp1 HG00544.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+1769T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159530 | ||||||
| chr11:33159595
|
C | CA | 46 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(43): Show | 49 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.27+1703dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | ||||||
| chr11:33159595
|
C | CAA | 63 | a0001c0001t0001g0196a0001c0001t0001g0308a0001c0001t0001g0309others(60): Show | 78 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.27+1702_27+1703dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | ||||||
| chr11:33159595
|
C | CAAA | 50 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(47): Show | 50 | HG00735.hp2 HG00741.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.27+1701_27+1703dup others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | ||||||
| chr11:33159595
|
C | CAAAA | 17 | a0001c0001t0001g0021a0001c0001t0001g0213a0001c0001t0001g0214others(14): Show | 18 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.27+1700_27+1703dup others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | ||||||
| chr11:33159595
|
C | CAAAAA | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG00642.hp2 HG03139.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+1699_27+1703dup others(5): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | ||||||
| chr11:33159595
|
CA | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0232a0001c0001t0001g0233others(10): Show | 17 | HG00323.hp1 HG01261.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.27+1703delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | ||||||
| chr11:33159664
|
G | A | 1 | a0001c0001t0003g0188 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.27+1635C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159664 | ||||||
| chr11:33159712
|
A | T | 1 | a0001c0001t0003g0028 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.27+1587T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159712 | ||||||
| chr11:33159731
|
T | C | 1 | a0001c0001t0001g0316 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.27+1568A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159731 | ||||||
| chr11:33159799
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+1500A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159799 | ||||||
| chr11:33159915
|
G | C | 1 | a0001c0001t0001g0317 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.27+1384C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159915 | ||||||
| chr11:33160321
|
C | T | 1 | a0001c0001t0002g0027 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.27+978G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160321 | ||||||
| chr11:33160572
|
TCTGAATA others(16): Show |
T | 1 | a0001c0001t0002g0026 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.27+704_27+726delTT others(21): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160572 | ||||||
| chr11:33160710
|
T | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG01891.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.27+589A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160710 | ||||||
| chr11:33160732
|
A | G | 38 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(35): Show | 38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+567T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160732 | ||||||
| chr11:33160762
|
G | A | 180 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(177): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+537C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160762 | ||||||
| chr11:33160825
|
T | C | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+474A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160825 | ||||||
| chr11:33160846
|
A | G | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0012others(176): Show | 201 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.27+453T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160846 | ||||||
| chr11:33161006
|
A | G | 1 | a0001c0003t0002g0024 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.27+293T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33161006 | ||||||
| chr11:33161088
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0189 | 3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+211C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33161088 | ||||||
| chr11:33161153
|
C | G | 1 | a0001c0001t0002g0023 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.27+146G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33161153 |