Search by Gene
| geneid | 26574 |
|---|---|
| ensemblid | ENSG00000275700.6 |
| hgncid | 19235 |
| symbol | AATF |
| name | apoptosis antagonizing transcription factor |
| refseq_nuc | NM_012138.4 |
| refseq_prot | NP_036270.1 |
| ensembl_nuc | ENST00000619387.5 |
| ensembl_prot | ENSP00000477848.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 36948954 |
| end | 37056871 |
| strand | + |
| ver | v1.2 |
| region | chr17:36948954-37056871 |
| region5000 | chr17:36943954-37061871 |
| regionname0 | AATF_chr17_36948954_37056871 |
| regionname5000 | AATF_chr17_36943954_37061871 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 560 | 233 | 78 | 43 | 80 | 8 | 23 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0002 | 0/0 | 560 | 5 | 2 | 0 | 2 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0003 | 0/0 | 560 | 4 | 4 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0004 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0005 | 0/0 | 560 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0006 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1683 | 192 | 64 | 35 | 70 | 6 | 16 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| c0002 | 0/0 | 1683 | 31 | 4 | 8 | 10 | 2 | 7 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| c0003 | 0/0 | 1683 | 9 | 9 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| c0004 | 0/0 | 1683 | 5 | 2 | 0 | 2 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| c0005 | 0/0 | 1683 | 3 | 3 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| c0006 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| c0007 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| c0008 | 0/0 | 1683 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| c0009 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| c0010 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 380 | 166 | 71 | 31 | 46 | 5 | 13 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| t0002 | 0/1 | 380 | 57 | 2 | 10 | 33 | 2 | 9 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| t0003 | 0/0 | 380 | 6 | 6 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| t0004 | 0/0 | 380 | 6 | 6 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| t0005 | 0/0 | 380 | 5 | 1 | 2 | 0 | 1 | 1 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| t0006 | 0/0 | 380 | 2 | 0 | 0 | 2 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| t0007 | 0/0 | 380 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| t0008 | 0/0 | 380 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| t0009 | 0/0 | 380 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/1 | 192 | 64 | 35 | 70 | 6 | 16 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 31 | 4 | 8 | 10 | 2 | 7 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0009 | a0001 | c0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0002c0004 | a0002 | c0004 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0003c0005 | a0003 | c0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0003c0007 | a0003 | c0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0004c0010 | a0004 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0005c0008 | a0005 | c0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0006c0006 | a0006 | c0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 147 | 56 | 30 | 44 | 5 | 12 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/1 | 34 | 1 | 4 | 23 | 1 | 4 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 23 | 1 | 6 | 10 | 1 | 5 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0002t0005 | a0001 | c0002 | t0005 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0002t0009 | a0001 | c0002 | t0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0003t0004 | a0001 | c0003 | t0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0001c0009t0001 | a0001 | c0009 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0002c0004t0001 | a0002 | c0004 | t0001 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0003c0005t0001 | a0003 | c0005 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0004c0010t0001 | a0004 | c0010 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0005c0008t0001 | a0005 | c0008 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| a0006c0006t0001 | a0006 | c0006 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0224 | a0001 | c0001 | t0001 | g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0230 | a0001 | c0001 | t0001 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0003 | a0001 | c0001 | t0002 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0005 | a0001 | c0001 | t0002 | g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0006 | a0001 | c0001 | t0002 | g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0007 | a0001 | c0001 | t0002 | g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0008 | a0001 | c0001 | t0002 | g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0009 | a0001 | c0001 | t0002 | g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0010 | a0001 | c0001 | t0002 | g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0012 | a0001 | c0001 | t0002 | g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0107 | a0001 | c0001 | t0002 | g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0110 | a0001 | c0001 | t0002 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0113 | a0001 | c0001 | t0002 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0114 | a0001 | c0001 | t0002 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0115 | a0001 | c0001 | t0002 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0143 | a0001 | c0001 | t0002 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0144 | a0001 | c0001 | t0002 | g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0145 | a0001 | c0001 | t0002 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0146 | a0001 | c0001 | t0002 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0148 | a0001 | c0001 | t0002 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0149 | a0001 | c0001 | t0002 | g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0150 | a0001 | c0001 | t0002 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0151 | a0001 | c0001 | t0002 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0154 | a0001 | c0001 | t0002 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0156 | a0001 | c0001 | t0002 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0157 | a0001 | c0001 | t0002 | g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0183 | a0001 | c0001 | t0002 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0206 | a0001 | c0001 | t0002 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0215 | a0001 | c0001 | t0002 | g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0216 | a0001 | c0001 | t0002 | g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0002g0219 | a0001 | c0001 | t0002 | g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0003g0016 | a0001 | c0001 | t0003 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0003g0075 | a0001 | c0001 | t0003 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0003g0076 | a0001 | c0001 | t0003 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0003g0077 | a0001 | c0001 | t0003 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0003g0078 | a0001 | c0001 | t0003 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0003g0079 | a0001 | c0001 | t0003 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0004g0244 | a0001 | c0001 | t0004 | g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0006g0048 | a0001 | c0001 | t0006 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0006g0222 | a0001 | c0001 | t0006 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0007g0225 | a0001 | c0001 | t0007 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0001t0008g0178 | a0001 | c0001 | t0008 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0001g0124 | a0001 | c0002 | t0001 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0001g0125 | a0001 | c0002 | t0001 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0109 | a0001 | c0002 | t0002 | g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0127 | a0001 | c0002 | t0002 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0128 | a0001 | c0002 | t0002 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0129 | a0001 | c0002 | t0002 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0130 | a0001 | c0002 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0131 | a0001 | c0002 | t0002 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0133 | a0001 | c0002 | t0002 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0135 | a0001 | c0002 | t0002 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0136 | a0001 | c0002 | t0002 | g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0137 | a0001 | c0002 | t0002 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0138 | a0001 | c0002 | t0002 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0140 | a0001 | c0002 | t0002 | g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0141 | a0001 | c0002 | t0002 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0142 | a0001 | c0002 | t0002 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0152 | a0001 | c0002 | t0002 | g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0155 | a0001 | c0002 | t0002 | g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0235 | a0001 | c0002 | t0002 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0236 | a0001 | c0002 | t0002 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0237 | a0001 | c0002 | t0002 | g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0238 | a0001 | c0002 | t0002 | g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0239 | a0001 | c0002 | t0002 | g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0240 | a0001 | c0002 | t0002 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0002g0241 | a0001 | c0002 | t0002 | g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0005g0117 | a0001 | c0002 | t0005 | g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0005g0126 | a0001 | c0002 | t0005 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0005g0132 | a0001 | c0002 | t0005 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0005g0134 | a0001 | c0002 | t0005 | g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0005g0139 | a0001 | c0002 | t0005 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0002t0009g0153 | a0001 | c0002 | t0009 | g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0003t0001g0034 | a0001 | c0003 | t0001 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0003t0001g0035 | a0001 | c0003 | t0001 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0003t0001g0080 | a0001 | c0003 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0003t0001g0091 | a0001 | c0003 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0003t0004g0037 | a0001 | c0003 | t0004 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0003t0004g0044 | a0001 | c0003 | t0004 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0003t0004g0045 | a0001 | c0003 | t0004 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0003t0004g0046 | a0001 | c0003 | t0004 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0003t0004g0047 | a0001 | c0003 | t0004 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0001c0009t0001g0164 | a0001 | c0009 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0002c0004t0001g0097 | a0002 | c0004 | t0001 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0002c0004t0001g0098 | a0002 | c0004 | t0001 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0002c0004t0001g0099 | a0002 | c0004 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AATF_chr17_36943954_37061871 | AATF |
| a0002c0004t0001g0100 | a0002 | c0004 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0002c0004t0001g0102 | a0002 | c0004 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0003c0005t0001g0013 | a0003 | c0005 | t0001 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0003c0005t0001g0093 | a0003 | c0005 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0003c0005t0001g0095 | a0003 | c0005 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0003c0007t0001g0094 | a0003 | c0007 | t0001 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0004c0010t0001g0018 | a0004 | c0010 | t0001 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0005c0008t0001g0101 | a0005 | c0008 | t0001 | g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| a0006c0006t0001g0036 | a0006 | c0006 | t0001 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AATF_chr17_36943954_37061871 | AATF |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | AATF_chr17_36943954_37061871 | AATF |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | AATF_chr17_36943954_37061871 | AATF |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | AATF_chr17_36943954_37061871 | AATF |
| HG00140 | hp2 | a0001 | c0002 | t0005 | g0134 | EUR | GBR | AATF_chr17_36943954_37061871 | AATF |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0136 | EUR | FIN | AATF_chr17_36943954_37061871 | AATF |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0206 | EUR | FIN | AATF_chr17_36943954_37061871 | AATF |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | AATF_chr17_36943954_37061871 | AATF |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | AATF_chr17_36943954_37061871 | AATF |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | AATF_chr17_36943954_37061871 | AATF |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | AATF_chr17_36943954_37061871 | AATF |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | AATF_chr17_36943954_37061871 | AATF |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | AATF_chr17_36943954_37061871 | AATF |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | CHS | AATF_chr17_36943954_37061871 | AATF |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | AATF_chr17_36943954_37061871 | AATF |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01070 | hp2 | a0001 | c0002 | t0005 | g0126 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01071 | hp1 | a0001 | c0002 | t0005 | g0132 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0235 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | AATF_chr17_36943954_37061871 | AATF |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0178 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0135 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | AATF_chr17_36943954_37061871 | AATF |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | AATF_chr17_36943954_37061871 | AATF |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | AATF_chr17_36943954_37061871 | AATF |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02015 | hp2 | a0001 | c0001 | t0007 | g0225 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02135 | hp2 | a0002 | c0004 | t0001 | g0102 | EAS | KHV | AATF_chr17_36943954_37061871 | AATF |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | AATF_chr17_36943954_37061871 | AATF |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | CDX | AATF_chr17_36943954_37061871 | AATF |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0139 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | AATF_chr17_36943954_37061871 | AATF |
| HG02293 | hp2 | a0005 | c0008 | t0001 | g0101 | AMR | PEL | AATF_chr17_36943954_37061871 | AATF |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | AATF_chr17_36943954_37061871 | AATF |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | AATF_chr17_36943954_37061871 | AATF |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02622 | hp2 | a0004 | c0010 | t0001 | g0018 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0138 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02647 | hp1 | a0003 | c0007 | t0001 | g0094 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02723 | hp1 | a0002 | c0004 | t0001 | g0098 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0047 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG02738 | hp1 | a0001 | c0002 | t0005 | g0117 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0044 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0080 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG03098 | hp1 | a0001 | c0003 | t0004 | g0045 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03098 | hp2 | a0003 | c0005 | t0001 | g0095 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | AATF_chr17_36943954_37061871 | AATF |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG03540 | hp1 | a0003 | c0005 | t0001 | g0013 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | AATF_chr17_36943954_37061871 | AATF |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0037 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0133 | SAS | PJL | AATF_chr17_36943954_37061871 | AATF |
| HG03834 | hp1 | a0002 | c0004 | t0001 | g0099 | SAS | BEB | AATF_chr17_36943954_37061871 | AATF |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | AATF_chr17_36943954_37061871 | AATF |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0130 | SAS | BEB | AATF_chr17_36943954_37061871 | AATF |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | AATF_chr17_36943954_37061871 | AATF |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | AATF_chr17_36943954_37061871 | AATF |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0155 | SAS | BEB | AATF_chr17_36943954_37061871 | AATF |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | AATF_chr17_36943954_37061871 | AATF |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0137 | SAS | STU | AATF_chr17_36943954_37061871 | AATF |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0140 | SAS | STU | AATF_chr17_36943954_37061871 | AATF |
| HG04228 | hp2 | a0001 | c0002 | t0009 | g0153 | SAS | STU | AATF_chr17_36943954_37061871 | AATF |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | AATF_chr17_36943954_37061871 | AATF |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | AATF_chr17_36943954_37061871 | AATF |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | CHB | AATF_chr17_36943954_37061871 | AATF |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | AATF_chr17_36943954_37061871 | AATF |
| NA18906 | hp1 | a0003 | c0005 | t0001 | g0093 | AFR | YRI | AATF_chr17_36943954_37061871 | AATF |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | AATF_chr17_36943954_37061871 | AATF |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0222 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | AATF_chr17_36943954_37061871 | AATF |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | AATF_chr17_36943954_37061871 | AATF |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | AATF_chr17_36943954_37061871 | AATF |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | AATF_chr17_36943954_37061871 | AATF |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19068 | hp1 | a0002 | c0004 | t0001 | g0100 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | AATF_chr17_36943954_37061871 | AATF |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0091 | AFR | YRI | AATF_chr17_36943954_37061871 | AATF |
| NA19240 | hp2 | a0001 | c0009 | t0001 | g0164 | AFR | YRI | AATF_chr17_36943954_37061871 | AATF |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ASW | AATF_chr17_36943954_37061871 | AATF |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | AATF_chr17_36943954_37061871 | AATF |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | AATF_chr17_36943954_37061871 | AATF |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | AATF_chr17_36943954_37061871 | AATF |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | GIH | AATF_chr17_36943954_37061871 | AATF |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | AATF_chr17_36943954_37061871 | AATF |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0035 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02486 | hp2 | a0001 | c0003 | t0004 | g0046 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | AATF_chr17_36943954_37061871 | AATF |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | AATF_chr17_36943954_37061871 | AATF |
| HG06807 | hp1 | a0002 | c0004 | t0001 | g0097 | AFR | USA | AATF_chr17_36943954_37061871 | AATF |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | USA | AATF_chr17_36943954_37061871 | AATF |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | USA | AATF_chr17_36943954_37061871 | AATF |
| NA20300 | hp2 | a0006 | c0006 | t0001 | g0036 | AFR | USA | AATF_chr17_36943954_37061871 | AATF |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0216 | REF | REF | AATF_chr17_36943954_37061871 | AATF |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:36950225
|
A | G | 1 | a0004 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.103A>G | p.Arg35Gly | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/12 | 275/2062 | 103/1683 | 35/560 | chr17 | 36950225 | ||
| chr17:36950372
|
G | A | 1 | a0006 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.250G>A | p.Asp84Asn | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/12 | 422/2062 | 250/1683 | 84/560 | chr17 | 36950372 | ||
| chr17:36952895
|
T | C | 1 | a0003 | 4 | HG02647.hp1 HG03098.hp2 HG03540.hp1 others(1): Show |
missense_variant | MODERATE | c.293T>C | p.Ile98Thr | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 3/12 | 465/2062 | 293/1683 | 98/560 | chr17 | 36952895 | ||
| chr17:36953122
|
G | A | 2 | a0002a0005 | 6 | HG02135.hp2 HG02293.hp2 HG02723.hp1 others(3): Show |
missense_variant | MODERATE | c.520G>A | p.Glu174Lys | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 3/12 | 692/2062 | 520/1683 | 174/560 | chr17 | 36953122 | ||
| chr17:37056614
|
C | T | 1 | a0005 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.1633C>T | p.Arg545Cys | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 12/12 | 1805/2062 | 1633/1683 | 545/560 | chr17 | 37056614 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:36988547
|
C | T | 1 | a0001c0009 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.976C>T | p.Leu326Leu | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 6/12 | 1148/2062 | 976/1683 | 326/560 | chr17 | 36988547 | ||
| chr17:36989342
|
T | C | 1 | a0001c0002 | 31 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(28): Show |
synonymous_variant | LOW | c.1245T>C | p.Ser415Ser | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 7/12 | 1417/2062 | 1245/1683 | 415/560 | chr17 | 36989342 | ||
| chr17:37019052
|
C | T | 4 | a0001c0003a0002c0004a0003c0007others(1): Show | 16 | HG02109.hp1 HG02135.hp2 HG02293.hp2 others(13): Show |
synonymous_variant | LOW | c.1446C>T | p.Asn482Asn | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 9/12 | 1618/2062 | 1446/1683 | 482/560 | chr17 | 37019052 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:36949012
|
G | C | 3 | a0001c0001t0002a0001c0002t0002a0001c0002t0005 | 62 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-114G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/12 | 114 | chr17 | 36949012 | |||||
| chr17:36949012
|
G | T | 2 | a0001c0001t0004a0001c0003t0004 | 6 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-114G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/12 | chr17 | 36949012 | ||||||
| chr17:36949028
|
A | G | 1 | a0001c0002t0009 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-98A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/12 | 98 | chr17 | 36949028 | |||||
| chr17:36949091
|
G | C | 1 | a0001c0001t0007 | 1 | HG02015.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-35G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/12 | chr17 | 36949091 | ||||||
| chr17:37056699
|
G | T | 1 | a0001c0001t0006 | 2 | NA18612.hp1 NA18992.hp1 |
3_prime_UTR_variant | MODIFIER | c.*35G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 12/12 | 35 | chr17 | 37056699 | |||||
| chr17:37056706
|
C | T | 2 | a0001c0001t0008a0001c0002t0005 | 6 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*42C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 12/12 | 42 | chr17 | 37056706 | |||||
| chr17:37056729
|
A | T | 1 | a0001c0002t0009 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*65A>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 12/12 | 65 | chr17 | 37056729 | |||||
| chr17:37056822
|
C | T | 1 | a0001c0001t0003 | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*158C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 12/12 | 158 | chr17 | 37056822 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:36949466
|
T | A | 11 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(8): Show | 11 | HG00408.hp1 HG00558.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+250T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | chr17 | 36949466 | ||||||
| chr17:36949574
|
A | G | 1 | a0001c0001t0004g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+358A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | chr17 | 36949574 | ||||||
| chr17:36949770
|
G | A | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(91): Show | 94 | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(91): Show |
intron_variant | MODIFIER | c.92-444G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | chr17 | 36949770 | ||||||
| chr17:36949778
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.92-436G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | chr17 | 36949778 | ||||||
| chr17:36949922
|
C | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG02257.hp1 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.92-292C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | chr17 | 36949922 | ||||||
| chr17:36950008
|
C | G | 1 | a0001c0001t0001g0243 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.92-206C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | chr17 | 36950008 | ||||||
| chr17:36950053
|
G | A | 1 | a0003c0005t0001g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.92-161G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | chr17 | 36950053 | ||||||
| chr17:36950077
|
G | A | 74 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(71): Show | 74 | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(71): Show |
intron_variant | MODIFIER | c.92-137G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | chr17 | 36950077 | ||||||
| chr17:36950474
|
T | C | 82 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(79): Show | 82 | HG00735.hp1 HG00735.hp2 HG01106.hp2 others(79): Show |
intron_variant | MODIFIER | c.283+69T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36950474 | ||||||
| chr17:36950477
|
C | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(1): Show | 4 | HG01109.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+72C>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36950477 | ||||||
| chr17:36950523
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(1): Show | 4 | HG01109.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+118G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36950523 | ||||||
| chr17:36950876
|
G | A | 1 | a0004c0010t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.283+471G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36950876 | ||||||
| chr17:36951001
|
A | G | 39 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(36): Show | 39 | HG00735.hp2 HG01167.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.283+596A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36951001 | ||||||
| chr17:36951086
|
T | A | 1 | a0001c0003t0004g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.283+681T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36951086 | ||||||
| chr17:36951165
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.283+760A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36951165 | ||||||
| chr17:36951296
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.283+891A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36951296 | ||||||
| chr17:36951388
|
G | T | 4 | a0003c0005t0001g0013a0003c0005t0001g0093a0003c0005t0001g0095others(1): Show | 4 | HG02647.hp1 HG03098.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+983G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36951388 | ||||||
| chr17:36951409
|
G | T | 2 | a0002c0004t0001g0102a0005c0008t0001g0101 | 2 | HG02135.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.283+1004G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36951409 | ||||||
| chr17:36951585
|
C | G | 9 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(6): Show | 9 | HG02622.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+1180C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36951585 | ||||||
| chr17:36951595
|
A | G | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(8): Show | 11 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+1190A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36951595 | ||||||
| chr17:36951798
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.284-1088T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36951798 | ||||||
| chr17:36952054
|
A | G | 7 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | HG02055.hp1 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-832A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36952054 | ||||||
| chr17:36952143
|
G | A | 1 | a0003c0005t0001g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-743G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36952143 | ||||||
| chr17:36952199
|
A | C | 6 | a0001c0002t0002g0236a0001c0002t0002g0237a0001c0002t0002g0238others(3): Show | 6 | HG00621.hp1 HG02155.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-687A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36952199 | ||||||
| chr17:36952214
|
C | G | 1 | a0001c0002t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.284-672C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36952214 | ||||||
| chr17:36952363
|
A | G | 15 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(12): Show | 16 | HG00738.hp2 HG01074.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-523A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36952363 | ||||||
| chr17:36952426
|
G | C | 87 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(84): Show | 87 | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.284-460G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36952426 | ||||||
| chr17:36952522
|
G | T | 1 | a0006c0006t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.284-364G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36952522 | ||||||
| chr17:36952548
|
A | C | 80 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 80 | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(77): Show |
intron_variant | MODIFIER | c.284-338A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36952548 | ||||||
| chr17:36952784
|
T | A | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.284-102T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | chr17 | 36952784 | ||||||
| chr17:36953331
|
A | C | 32 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(29): Show | 32 | HG01106.hp2 HG01192.hp2 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.694+35A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 3/11 | chr17 | 36953331 | ||||||
| chr17:36953344
|
T | G | 1 | a0001c0001t0001g0242 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.694+48T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 3/11 | chr17 | 36953344 | ||||||
| chr17:36953383
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.694+87A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 3/11 | chr17 | 36953383 | ||||||
| chr17:36953685
|
G | C | 7 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.695-85G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 3/11 | chr17 | 36953685 | ||||||
| chr17:36953914
|
A | C | 1 | a0006c0006t0001g0036 | 1 | NA20300.hp2 | splice_region_variant&intron_variant | LOW | c.832+7A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36953914 | ||||||
| chr17:36954065
|
C | CT | 20 | a0001c0001t0001g0017a0001c0001t0001g0081a0001c0001t0001g0082others(17): Show | 20 | HG01175.hp1 HG02135.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.832+178dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36954065 | |||||
| chr17:36954139
|
G | C | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(91): Show | 94 | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(91): Show |
intron_variant | MODIFIER | c.832+232G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36954139 | ||||||
| chr17:36954153
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+246G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36954153 | ||||||
| chr17:36954220
|
G | A | 1 | a0001c0002t0002g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.832+313G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36954220 | ||||||
| chr17:36954321
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.832+414A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36954321 | ||||||
| chr17:36954393
|
C | A | 3 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115 | 3 | NA18940.hp2 NA18985.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.832+486C>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36954393 | ||||||
| chr17:36954402
|
T | C | 1 | a0001c0002t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.832+495T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36954402 | ||||||
| chr17:36954445
|
A | G | 1 | a0001c0001t0004g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+538A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36954445 | ||||||
| chr17:36954843
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.832+936T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36954843 | ||||||
| chr17:36954972
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832+1065T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36954972 | ||||||
| chr17:36955128
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.832+1221C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955128 | ||||||
| chr17:36955156
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.832+1249G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955156 | ||||||
| chr17:36955157
|
A | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.832+1250A>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955157 | ||||||
| chr17:36955202
|
T | A | 1 | a0001c0002t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.832+1295T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955202 | ||||||
| chr17:36955216
|
A | G | 3 | a0001c0001t0001g0242a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01074.hp1 NA20905.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.832+1309A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955216 | ||||||
| chr17:36955300
|
G | A | 1 | a0001c0002t0005g0117 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.832+1393G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955300 | ||||||
| chr17:36955694
|
T | A | 35 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(32): Show | 35 | HG01106.hp2 HG01192.hp2 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.832+1787T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955694 | ||||||
| chr17:36955781
|
G | A | 46 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(43): Show | 46 | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.832+1874G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955781 | ||||||
| chr17:36955797
|
C | T | 1 | a0006c0006t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.832+1890C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955797 | ||||||
| chr17:36955872
|
C | T | 13 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(10): Show | 13 | HG02055.hp1 HG02135.hp2 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.832+1965C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36955872 | ||||||
| chr17:36956204
|
G | A | 6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02055.hp1 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+2297G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36956204 | ||||||
| chr17:36956395
|
G | A | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | NA18963.hp1 NA19004.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+2488G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36956395 | ||||||
| chr17:36956479
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18953.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.832+2572C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36956479 | ||||||
| chr17:36956563
|
C | T | 1 | a0001c0001t0004g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+2656C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36956563 | ||||||
| chr17:36956565
|
C | T | 1 | a0001c0001t0004g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+2658C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36956565 | ||||||
| chr17:36956605
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.832+2698G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36956605 | ||||||
| chr17:36956616
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(14): Show | 17 | HG01891.hp2 HG02109.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.832+2709C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36956616 | ||||||
| chr17:36956759
|
T | A | 1 | a0004c0010t0001g0018 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.832+2852T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36956759 | ||||||
| chr17:36956979
|
G | GA | 12 | a0001c0001t0001g0081a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.832+3082dupA | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36956979 | |||||
| chr17:36957344
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.832+3437T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36957344 | ||||||
| chr17:36957432
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.832+3525T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36957432 | ||||||
| chr17:36957618
|
G | A | 1 | a0001c0001t0004g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+3711G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36957618 | ||||||
| chr17:36957928
|
A | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(7): Show | 10 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.832+4021A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36957928 | ||||||
| chr17:36957954
|
A | G | 73 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(70): Show | 73 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(70): Show |
intron_variant | MODIFIER | c.832+4047A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36957954 | ||||||
| chr17:36958155
|
CTCTT | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+4254_832+4257d others(6): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36958155 | |||||
| chr17:36958167
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0006g0222 | 2 | NA18612.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.832+4260T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958167 | ||||||
| chr17:36958170
|
C | CT | 21 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0001g0108others(18): Show | 21 | HG02109.hp1 HG02135.hp2 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.832+4273dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36958170 | |||||
| chr17:36958313
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0084others(2): Show | 5 | HG01109.hp1 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+4406C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958313 | ||||||
| chr17:36958319
|
C | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+4412C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958319 | ||||||
| chr17:36958369
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+4462G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958369 | ||||||
| chr17:36958400
|
T | C | 25 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(22): Show | 25 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+4493T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958400 | ||||||
| chr17:36958454
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+4547T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958454 | ||||||
| chr17:36958456
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+4549T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958456 | ||||||
| chr17:36958510
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+4603T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958510 | ||||||
| chr17:36958677
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.832+4770G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958677 | ||||||
| chr17:36958698
|
A | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+4791A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958698 | ||||||
| chr17:36958916
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.832+5009A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958916 | ||||||
| chr17:36958974
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+5067G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958974 | ||||||
| chr17:36958998
|
T | G | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+5091T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36958998 | ||||||
| chr17:36959126
|
C | CAA | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+5219_832+5220i others(4): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36959126 | ||||||
| chr17:36959139
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+5232G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36959139 | ||||||
| chr17:36959273
|
G | A | 59 | a0001c0001t0001g0147a0001c0001t0001g0242a0001c0001t0002g0001others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.832+5366G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36959273 | ||||||
| chr17:36959464
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.832+5557A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36959464 | ||||||
| chr17:36959489
|
G | T | 1 | a0001c0001t0001g0067 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.832+5582G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36959489 | ||||||
| chr17:36959541
|
G | A | 2 | a0002c0004t0001g0097a0002c0004t0001g0098 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.832+5634G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36959541 | ||||||
| chr17:36959571
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG01891.hp1 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+5664C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36959571 | ||||||
| chr17:36959851
|
A | G | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(57): Show | 60 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(57): Show |
intron_variant | MODIFIER | c.832+5944A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36959851 | ||||||
| chr17:36959901
|
A | G | 25 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(22): Show | 25 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+5994A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36959901 | ||||||
| chr17:36960018
|
T | C | 2 | a0001c0002t0001g0124a0001c0002t0001g0125 | 2 | HG02055.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.832+6111T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960018 | ||||||
| chr17:36960023
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0223 | 2 | HG02976.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.832+6116T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960023 | ||||||
| chr17:36960023
|
TC | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+6124delC | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36960023 | |||||
| chr17:36960025
|
C | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+6118C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960025 | ||||||
| chr17:36960029
|
C | G | 1 | a0001c0002t0002g0241 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.832+6122C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960029 | ||||||
| chr17:36960055
|
C | T | 1 | a0001c0002t0002g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.832+6148C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960055 | ||||||
| chr17:36960099
|
T | C | 162 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(159): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.832+6192T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960099 | ||||||
| chr17:36960107
|
G | A | 1 | a0001c0001t0006g0048 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.832+6200G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960107 | ||||||
| chr17:36960173
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.832+6266C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960173 | ||||||
| chr17:36960192
|
G | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+6285G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960192 | ||||||
| chr17:36960384
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.832+6477C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960384 | ||||||
| chr17:36960412
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 6 | HG02257.hp1 HG02622.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+6505G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960412 | ||||||
| chr17:36960456
|
G | GT | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 6 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.832+6550dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36960456 | |||||
| chr17:36960548
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.832+6641G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960548 | ||||||
| chr17:36960554
|
A | C | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+6647A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960554 | ||||||
| chr17:36960618
|
T | C | 43 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 43 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.832+6711T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36960618 | ||||||
| chr17:36961044
|
C | T | 4 | a0001c0001t0003g0076a0001c0001t0003g0077a0001c0001t0003g0078others(1): Show | 4 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+7137C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961044 | ||||||
| chr17:36961069
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+7162G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961069 | ||||||
| chr17:36961099
|
T | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+7192T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961099 | ||||||
| chr17:36961100
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+7193T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961100 | ||||||
| chr17:36961103
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | NA18953.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.832+7196A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961103 | ||||||
| chr17:36961170
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+7263G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961170 | ||||||
| chr17:36961191
|
T | G | 1 | a0003c0005t0001g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.832+7284T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961191 | ||||||
| chr17:36961247
|
A | T | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(50): Show | 53 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(50): Show |
intron_variant | MODIFIER | c.832+7340A>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961247 | ||||||
| chr17:36961440
|
T | C | 58 | a0001c0001t0001g0147a0001c0001t0002g0001a0001c0001t0002g0002others(55): Show | 59 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.832+7533T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961440 | ||||||
| chr17:36961658
|
A | G | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+7751A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961658 | ||||||
| chr17:36961674
|
AT | A | 22 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(19): Show | 22 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.832+7781delT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36961674 | |||||
| chr17:36961765
|
G | C | 59 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(56): Show | 59 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(56): Show |
intron_variant | MODIFIER | c.832+7858G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961765 | ||||||
| chr17:36961848
|
T | C | 1 | a0001c0001t0004g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+7941T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961848 | ||||||
| chr17:36961964
|
G | A | 1 | a0001c0003t0004g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.832+8057G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961964 | ||||||
| chr17:36961999
|
C | T | 28 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(25): Show | 28 | HG01891.hp1 HG02109.hp1 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.832+8092C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36961999 | ||||||
| chr17:36962022
|
A | G | 25 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(22): Show | 25 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+8115A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962022 | ||||||
| chr17:36962025
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(6): Show | 9 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.832+8118C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962025 | ||||||
| chr17:36962118
|
T | G | 1 | a0001c0001t0001g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.832+8211T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962118 | ||||||
| chr17:36962314
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.832+8407G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962314 | ||||||
| chr17:36962450
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+8543T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962450 | ||||||
| chr17:36962485
|
C | A | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+8578C>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962485 | ||||||
| chr17:36962534
|
G | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+8627G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962534 | ||||||
| chr17:36962565
|
A | AT | 19 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0002g0115others(16): Show | 19 | HG02109.hp1 HG02135.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.832+8673dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36962565 | |||||
| chr17:36962565
|
A | ATT | 9 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+8672_832+8673d others(4): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36962565 | |||||
| chr17:36962565
|
AT | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(9): Show | 12 | HG01109.hp1 HG01981.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.832+8673delT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36962565 | |||||
| chr17:36962600
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.832+8693C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962600 | ||||||
| chr17:36962624
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.832+8717G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962624 | ||||||
| chr17:36962801
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(6): Show | 9 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.832+8894C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962801 | ||||||
| chr17:36962802
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+8895G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962802 | ||||||
| chr17:36962885
|
G | T | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+8978G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962885 | ||||||
| chr17:36962886
|
C | T | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+8979C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962886 | ||||||
| chr17:36962889
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.832+8982A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962889 | ||||||
| chr17:36962897
|
G | A | 38 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(35): Show | 38 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.832+8990G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36962897 | ||||||
| chr17:36963011
|
C | T | 1 | a0003c0007t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.832+9104C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963011 | ||||||
| chr17:36963044
|
G | C | 1 | a0001c0001t0004g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+9137G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963044 | ||||||
| chr17:36963080
|
T | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(6): Show | 9 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.832+9173T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963080 | ||||||
| chr17:36963085
|
C | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+9178C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963085 | ||||||
| chr17:36963110
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+9203T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963110 | ||||||
| chr17:36963227
|
T | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+9320T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963227 | ||||||
| chr17:36963318
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.832+9411A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963318 | ||||||
| chr17:36963321
|
A | G | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+9414A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963321 | ||||||
| chr17:36963376
|
C | T | 2 | a0001c0003t0001g0034a0001c0003t0001g0035 | 2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.832+9469C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963376 | ||||||
| chr17:36963539
|
T | G | 5 | a0001c0001t0001g0096a0002c0004t0001g0099a0002c0004t0001g0100others(2): Show | 5 | HG02135.hp2 HG02293.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+9632T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963539 | ||||||
| chr17:36963546
|
G | A | 16 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(13): Show | 16 | HG01891.hp1 HG02135.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.832+9639G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963546 | ||||||
| chr17:36963583
|
T | A | 7 | a0001c0001t0001g0096a0002c0004t0001g0097a0002c0004t0001g0098others(4): Show | 7 | HG02135.hp2 HG02293.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+9676T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963583 | ||||||
| chr17:36963645
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832+9738G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963645 | ||||||
| chr17:36963891
|
G | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+9984G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963891 | ||||||
| chr17:36963914
|
C | T | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0086others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.832+10007C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963914 | ||||||
| chr17:36963957
|
A | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+10050A>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36963957 | ||||||
| chr17:36964041
|
C | CA | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+10141dupA | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36964041 | |||||
| chr17:36964155
|
A | G | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+10248A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964155 | ||||||
| chr17:36964169
|
G | GC | 9 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(6): Show | 9 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.832+10263dupC | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36964169 | |||||
| chr17:36964170
|
C | CT | 10 | a0001c0001t0001g0031a0001c0001t0001g0212a0001c0001t0002g0114others(7): Show | 10 | HG01071.hp2 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.832+10283dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36964170 | |||||
| chr17:36964170
|
CT | C | 29 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0051others(26): Show | 29 | HG00099.hp2 HG00408.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.832+10283delT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36964170 | |||||
| chr17:36964170
|
CTT | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 16 | HG01243.hp2 HG01891.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.832+10282_832+1028 others(6): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36964170 | |||||
| chr17:36964171
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.832+10264T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964171 | ||||||
| chr17:36964174
|
T | G | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.832+10267T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964174 | ||||||
| chr17:36964175
|
T | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.832+10268T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964175 | ||||||
| chr17:36964199
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+10292G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964199 | ||||||
| chr17:36964212
|
TG | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+10306delG | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964212 | ||||||
| chr17:36964305
|
T | TG | 12 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0042others(9): Show | 12 | HG01243.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.832+10402dupG | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36964305 | |||||
| chr17:36964353
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.832+10446A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964353 | ||||||
| chr17:36964438
|
T | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(20): Show | 23 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.832+10531T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964438 | ||||||
| chr17:36964763
|
C | G | 39 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(36): Show | 39 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+10856C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964763 | ||||||
| chr17:36964784
|
C | T | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+10877C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964784 | ||||||
| chr17:36964916
|
G | C | 56 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0024others(53): Show | 56 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(53): Show |
intron_variant | MODIFIER | c.832+11009G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964916 | ||||||
| chr17:36964984
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.832+11077G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964984 | ||||||
| chr17:36964990
|
A | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.832+11083A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36964990 | ||||||
| chr17:36965245
|
G | T | 1 | a0001c0002t0001g0125 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.832+11338G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36965245 | ||||||
| chr17:36965277
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.832+11370G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36965277 | ||||||
| chr17:36965403
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.832+11496A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36965403 | ||||||
| chr17:36965772
|
G | C | 5 | a0001c0001t0001g0096a0002c0004t0001g0099a0002c0004t0001g0100others(2): Show | 5 | HG02135.hp2 HG02293.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+11865G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36965772 | ||||||
| chr17:36965844
|
G | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+11937G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36965844 | ||||||
| chr17:36965848
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.832+11941G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36965848 | ||||||
| chr17:36966002
|
A | C | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0086others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.832+12095A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36966002 | ||||||
| chr17:36966065
|
A | G | 1 | a0001c0001t0004g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+12158A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36966065 | ||||||
| chr17:36966220
|
T | A | 2 | a0001c0001t0001g0052a0001c0001t0006g0048 | 2 | HG00735.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.832+12313T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36966220 | ||||||
| chr17:36966682
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.832+12775T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36966682 | ||||||
| chr17:36966685
|
T | G | 10 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(7): Show | 10 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.832+12778T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36966685 | ||||||
| chr17:36966864
|
A | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+12957A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36966864 | ||||||
| chr17:36966982
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.832+13075T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36966982 | ||||||
| chr17:36967015
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.832+13108A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36967015 | ||||||
| chr17:36967440
|
A | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+13533A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36967440 | ||||||
| chr17:36967563
|
A | G | 1 | a0003c0005t0001g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.832+13656A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36967563 | ||||||
| chr17:36967626
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.832+13719C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36967626 | ||||||
| chr17:36967653
|
TC | T | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+13748delC | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36967653 | |||||
| chr17:36967711
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.832+13804A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36967711 | ||||||
| chr17:36967745
|
T | G | 1 | a0006c0006t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.832+13838T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36967745 | ||||||
| chr17:36967760
|
A | G | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG02280.hp1 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+13853A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36967760 | ||||||
| chr17:36967861
|
C | CT | 6 | a0001c0001t0001g0061a0001c0001t0001g0232a0001c0001t0002g0219others(3): Show | 6 | HG01106.hp1 HG01175.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.832+13971dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36967861 | |||||
| chr17:36967861
|
CT | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(18): Show | 21 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.832+13971delT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36967861 | |||||
| chr17:36967861
|
CTT | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.832+13970_832+1397 others(6): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36967861 | |||||
| chr17:36967946
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.832+14039G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36967946 | ||||||
| chr17:36968008
|
A | G | 88 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(85): Show | 89 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.832+14101A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968008 | ||||||
| chr17:36968223
|
A | T | 87 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(84): Show | 88 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.832+14316A>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968223 | ||||||
| chr17:36968234
|
TTTTTTTC | T | 80 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0025others(77): Show | 81 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.832+14340_832+1434 others(11): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968234 | |||||
| chr17:36968246
|
T | TC | 4 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0033others(1): Show | 4 | HG01109.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+14339_832+1434 others(5): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968246 | ||||||
| chr17:36968248
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0033others(1): Show | 4 | HG01109.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+14341C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968248 | ||||||
| chr17:36968250
|
T | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(4): Show | 7 | HG01109.hp1 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+14343T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968250 | ||||||
| chr17:36968255
|
T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0033others(1): Show | 4 | HG01109.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+14348T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968255 | ||||||
| chr17:36968259
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0085a0003c0005t0001g0013 | 3 | HG02976.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.832+14352T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968259 | ||||||
| chr17:36968261
|
TCC | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0084 | 3 | HG02258.hp1 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.832+14355_832+1435 others(6): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968261 | ||||||
| chr17:36968263
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0085a0003c0005t0001g0013 | 3 | HG01109.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.832+14356C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968263 | ||||||
| chr17:36968263
|
CTTCTTTC others(7): Show |
C | 1 | a0001c0001t0002g0114 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.832+14359_832+1437 others(18): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968263 | |||||
| chr17:36968266
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(4): Show | 7 | HG01109.hp1 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+14359C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968266 | ||||||
| chr17:36968266
|
CTTTCT | C | 6 | a0001c0001t0001g0030a0001c0003t0001g0034a0001c0003t0001g0035others(3): Show | 6 | HG02109.hp1 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.832+14363_832+1436 others(9): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968266 | |||||
| chr17:36968266
|
CTTTCTT | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG01891.hp1 HG02135.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.832+14363_832+1436 others(10): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968266 | |||||
| chr17:36968266
|
CTTTCTTT others(7): Show |
C | 17 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.832+14363_832+1437 others(18): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968266 | |||||
| chr17:36968266
|
CTTTCTTT others(8): Show |
C | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0011others(2): Show | 5 | HG02027.hp1 HG02083.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+14363_832+1437 others(19): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968266 | |||||
| chr17:36968266
|
CTTTCTTT others(9): Show |
C | 32 | a0001c0001t0001g0147a0001c0001t0002g0001a0001c0001t0002g0002others(29): Show | 33 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.832+14363_832+1437 others(20): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968266 | |||||
| chr17:36968270
|
C | CT | 5 | a0001c0001t0001g0112a0001c0001t0001g0207a0001c0001t0001g0208others(2): Show | 5 | HG02083.hp1 HG02132.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+14393dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968270 | |||||
| chr17:36968270
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(4): Show | 7 | HG01109.hp1 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+14363C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968270 | ||||||
| chr17:36968270
|
CT | C | 98 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0001g0049others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.832+14393delT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968270 | |||||
| chr17:36968270
|
CTT | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+14392_832+1439 others(6): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36968270 | |||||
| chr17:36968278
|
T | C | 1 | a0001c0001t0002g0114 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.832+14371T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968278 | ||||||
| chr17:36968281
|
T | C | 1 | a0001c0001t0002g0114 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.832+14374T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968281 | ||||||
| chr17:36968344
|
G | A | 87 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(84): Show | 88 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.832+14437G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968344 | ||||||
| chr17:36968368
|
G | A | 1 | a0001c0009t0001g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.832+14461G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968368 | ||||||
| chr17:36968431
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.832+14524C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968431 | ||||||
| chr17:36968556
|
G | A | 3 | a0001c0001t0001g0081a0003c0005t0001g0093a0003c0005t0001g0095 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.832+14649G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968556 | ||||||
| chr17:36968633
|
T | C | 1 | a0003c0005t0001g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.832+14726T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968633 | ||||||
| chr17:36968812
|
G | A | 3 | a0001c0001t0001g0081a0003c0005t0001g0093a0003c0005t0001g0095 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.832+14905G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968812 | ||||||
| chr17:36968866
|
G | A | 32 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(29): Show | 32 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.832+14959G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968866 | ||||||
| chr17:36968986
|
G | T | 33 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(30): Show | 33 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.832+15079G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36968986 | ||||||
| chr17:36969056
|
TC | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 14 | HG01891.hp1 HG02135.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+15151delC | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36969056 | |||||
| chr17:36969129
|
G | T | 1 | a0001c0009t0001g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.832+15222G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969129 | ||||||
| chr17:36969160
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0108 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.832+15253A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969160 | ||||||
| chr17:36969239
|
G | T | 1 | a0003c0007t0001g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.832+15332G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969239 | ||||||
| chr17:36969287
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.832+15380G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969287 | ||||||
| chr17:36969553
|
C | G | 30 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(27): Show | 30 | HG01891.hp1 HG02109.hp1 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.832+15646C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969553 | ||||||
| chr17:36969641
|
G | T | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.832+15734G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969641 | ||||||
| chr17:36969727
|
C | T | 1 | a0002c0004t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.832+15820C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969727 | ||||||
| chr17:36969729
|
G | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832+15822G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969729 | ||||||
| chr17:36969817
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.832+15910C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969817 | ||||||
| chr17:36969954
|
A | C | 1 | a0001c0009t0001g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.832+16047A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969954 | ||||||
| chr17:36969957
|
C | T | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+16050C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969957 | ||||||
| chr17:36969998
|
T | C | 8 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.832+16091T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969998 | ||||||
| chr17:36969999
|
G | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.832+16092G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36969999 | ||||||
| chr17:36970008
|
T | C | 1 | a0001c0002t0009g0153 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.832+16101T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970008 | ||||||
| chr17:36970093
|
A | T | 1 | a0001c0001t0001g0211 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.832+16186A>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970093 | ||||||
| chr17:36970276
|
T | G | 1 | a0001c0001t0002g0110 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.833-16341T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970276 | ||||||
| chr17:36970317
|
G | C | 31 | a0001c0001t0001g0096a0001c0001t0001g0147a0001c0001t0001g0242others(28): Show | 32 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.833-16300G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970317 | ||||||
| chr17:36970332
|
G | A | 1 | a0003c0005t0001g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.833-16285G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970332 | ||||||
| chr17:36970396
|
T | G | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0243 | 3 | NA18963.hp1 NA19057.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.833-16221T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970396 | ||||||
| chr17:36970534
|
CTTTTTTC others(5): Show |
C | 30 | a0001c0001t0001g0147a0001c0001t0001g0242a0001c0001t0002g0001others(27): Show | 31 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.833-16076_833-1606 others(16): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36970534 | |||||
| chr17:36970538
|
T | C | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(57): Show | 60 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(57): Show |
intron_variant | MODIFIER | c.833-16079T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970538 | ||||||
| chr17:36970539
|
TTC | T | 8 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0003g0075others(5): Show | 8 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.833-16076_833-1607 others(6): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36970539 | |||||
| chr17:36970540
|
TC | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(35): Show | 38 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.833-16076delC | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970540 | ||||||
| chr17:36970541
|
C | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(11): Show | 14 | HG01109.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.833-16076C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970541 | ||||||
| chr17:36970762
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.833-15855G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970762 | ||||||
| chr17:36970827
|
G | A | 1 | a0001c0003t0004g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.833-15790G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970827 | ||||||
| chr17:36970913
|
G | A | 3 | a0001c0001t0001g0081a0003c0005t0001g0093a0003c0005t0001g0095 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.833-15704G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970913 | ||||||
| chr17:36970982
|
A | G | 3 | a0001c0001t0001g0081a0003c0005t0001g0093a0003c0005t0001g0095 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.833-15635A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36970982 | ||||||
| chr17:36971036
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.833-15581A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36971036 | ||||||
| chr17:36971048
|
G | T | 90 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(87): Show | 91 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.833-15569G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36971048 | ||||||
| chr17:36971166
|
G | A | 91 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(88): Show | 92 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.833-15451G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36971166 | ||||||
| chr17:36971359
|
C | T | 42 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(39): Show | 42 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.833-15258C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36971359 | ||||||
| chr17:36971561
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.833-15056T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36971561 | ||||||
| chr17:36971750
|
C | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.833-14867C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36971750 | ||||||
| chr17:36971810
|
A | G | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.833-14807A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36971810 | ||||||
| chr17:36971912
|
G | C | 1 | a0001c0001t0001g0061 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.833-14705G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36971912 | ||||||
| chr17:36972181
|
G | A | 30 | a0001c0001t0001g0147a0001c0001t0001g0242a0001c0001t0002g0001others(27): Show | 31 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.833-14436G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36972181 | ||||||
| chr17:36972372
|
A | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0003c0005t0001g0013 | 3 | HG02809.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.833-14245A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36972372 | ||||||
| chr17:36972413
|
G | T | 8 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.833-14204G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36972413 | ||||||
| chr17:36972671
|
AT | A | 49 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(46): Show | 49 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.833-13931delT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36972671 | |||||
| chr17:36972671
|
ATT | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.833-13932_833-1393 others(6): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36972671 | |||||
| chr17:36972671
|
ATTT | A | 30 | a0001c0001t0001g0147a0001c0001t0001g0242a0001c0001t0002g0001others(27): Show | 31 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.833-13933_833-1393 others(7): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36972671 | |||||
| chr17:36972672
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.833-13945T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36972672 | ||||||
| chr17:36972803
|
T | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0092others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-13814T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36972803 | ||||||
| chr17:36972886
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.833-13731C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36972886 | ||||||
| chr17:36972933
|
A | G | 45 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(42): Show | 45 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.833-13684A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36972933 | ||||||
| chr17:36973083
|
A | G | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(91): Show | 95 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.833-13534A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36973083 | ||||||
| chr17:36973127
|
C | CT | 92 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(89): Show | 93 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.833-13484dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36973127 | |||||
| chr17:36973288
|
A | G | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(91): Show | 95 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.833-13329A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36973288 | ||||||
| chr17:36973520
|
G | A | 1 | a0001c0009t0001g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.833-13097G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36973520 | ||||||
| chr17:36973537
|
A | G | 29 | a0001c0002t0002g0109a0001c0002t0002g0127a0001c0002t0002g0128others(26): Show | 29 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.833-13080A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36973537 | ||||||
| chr17:36973785
|
A | G | 6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02055.hp1 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.833-12832A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36973785 | ||||||
| chr17:36973958
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.833-12659C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36973958 | ||||||
| chr17:36974048
|
G | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 16 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.833-12569G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36974048 | ||||||
| chr17:36974056
|
G | A | 1 | a0001c0009t0001g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.833-12561G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36974056 | ||||||
| chr17:36974064
|
A | G | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(91): Show | 95 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.833-12553A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36974064 | ||||||
| chr17:36974068
|
C | CA | 67 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(64): Show | 68 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.833-12536dupA | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36974068 | |||||
| chr17:36974068
|
C | CAA | 14 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(11): Show | 14 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-12537_833-1253 others(6): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36974068 | |||||
| chr17:36974174
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.833-12443A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36974174 | ||||||
| chr17:36974237
|
T | C | 31 | a0001c0001t0001g0096a0001c0001t0001g0147a0001c0001t0001g0242others(28): Show | 32 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.833-12380T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36974237 | ||||||
| chr17:36974322
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.833-12295A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36974322 | ||||||
| chr17:36974431
|
T | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(10): Show | 13 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.833-12186T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36974431 | ||||||
| chr17:36974555
|
A | G | 1 | a0001c0009t0001g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.833-12062A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36974555 | ||||||
| chr17:36975105
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.833-11512A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36975105 | ||||||
| chr17:36975441
|
T | A | 107 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(104): Show | 108 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.833-11176T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36975441 | ||||||
| chr17:36975477
|
G | A | 4 | a0002c0004t0001g0099a0002c0004t0001g0100a0002c0004t0001g0102others(1): Show | 4 | HG02135.hp2 HG02293.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-11140G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36975477 | ||||||
| chr17:36975844
|
T | G | 1 | a0001c0002t0002g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.833-10773T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36975844 | ||||||
| chr17:36975908
|
A | G | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(91): Show | 95 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.833-10709A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36975908 | ||||||
| chr17:36975932
|
A | G | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(91): Show | 95 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.833-10685A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36975932 | ||||||
| chr17:36976034
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.833-10583T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36976034 | ||||||
| chr17:36976241
|
C | T | 4 | a0001c0001t0001g0123a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG00621.hp2 HG01070.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-10376C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36976241 | ||||||
| chr17:36976260
|
T | A | 3 | a0001c0003t0001g0034a0001c0003t0001g0035a0001c0003t0001g0080 | 3 | HG02109.hp1 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.833-10357T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36976260 | ||||||
| chr17:36976291
|
T | C | 3 | a0001c0003t0004g0037a0001c0003t0004g0044a0001c0003t0004g0047 | 3 | HG02723.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.833-10326T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36976291 | ||||||
| chr17:36976507
|
G | A | 91 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(88): Show | 92 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.833-10110G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36976507 | ||||||
| chr17:36976569
|
G | A | 2 | a0001c0003t0004g0045a0001c0003t0004g0046 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.833-10048G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36976569 | ||||||
| chr17:36977497
|
T | A | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG02280.hp1 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-9120T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36977497 | ||||||
| chr17:36977545
|
T | G | 3 | a0001c0001t0001g0081a0003c0005t0001g0093a0003c0005t0001g0095 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.833-9072T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36977545 | ||||||
| chr17:36977638
|
A | G | 30 | a0001c0001t0001g0147a0001c0001t0001g0242a0001c0001t0002g0001others(27): Show | 31 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.833-8979A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36977638 | ||||||
| chr17:36977677
|
A | G | 18 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(15): Show | 18 | HG01891.hp1 HG02135.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.833-8940A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36977677 | ||||||
| chr17:36977732
|
C | A | 7 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0086others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.833-8885C>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36977732 | ||||||
| chr17:36977828
|
A | G | 12 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.833-8789A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36977828 | ||||||
| chr17:36978019
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0002g0143a0001c0001t0002g0151 | 3 | HG02083.hp2 NA19065.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.833-8598T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36978019 | ||||||
| chr17:36978252
|
A | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.833-8365A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36978252 | ||||||
| chr17:36978332
|
G | A | 29 | a0001c0001t0001g0147a0001c0001t0001g0242a0001c0001t0002g0001others(26): Show | 30 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.833-8285G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36978332 | ||||||
| chr17:36978409
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.833-8208G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36978409 | ||||||
| chr17:36978448
|
G | A | 24 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(21): Show | 24 | HG00735.hp2 HG01167.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.833-8169G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36978448 | ||||||
| chr17:36978723
|
A | G | 3 | a0001c0001t0001g0081a0003c0005t0001g0093a0003c0005t0001g0095 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.833-7894A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36978723 | ||||||
| chr17:36978935
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.833-7682T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36978935 | ||||||
| chr17:36979358
|
G | C | 1 | a0001c0003t0004g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.833-7259G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36979358 | ||||||
| chr17:36979481
|
G | A | 1 | a0001c0001t0003g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.833-7136G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36979481 | ||||||
| chr17:36979554
|
T | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0092others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-7063T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36979554 | ||||||
| chr17:36979643
|
G | A | 3 | a0001c0001t0001g0081a0003c0005t0001g0093a0003c0005t0001g0095 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.833-6974G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36979643 | ||||||
| chr17:36979795
|
A | T | 1 | a0001c0002t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.833-6822A>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36979795 | ||||||
| chr17:36979807
|
G | A | 29 | a0001c0001t0001g0147a0001c0001t0001g0242a0001c0001t0002g0001others(26): Show | 30 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.833-6810G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36979807 | ||||||
| chr17:36980246
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.833-6371A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36980246 | ||||||
| chr17:36980611
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.833-6006A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36980611 | ||||||
| chr17:36980898
|
C | CT | 39 | a0001c0001t0001g0015a0001c0001t0001g0062a0001c0001t0001g0063others(36): Show | 40 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.833-5701dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36980898 | |||||
| chr17:36980992
|
C | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.833-5625C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36980992 | ||||||
| chr17:36981067
|
G | C | 53 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(50): Show | 53 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.833-5550G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36981067 | ||||||
| chr17:36981233
|
C | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.833-5384C>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36981233 | ||||||
| chr17:36981378
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.833-5239C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36981378 | ||||||
| chr17:36981446
|
T | C | 6 | a0001c0003t0004g0037a0001c0003t0004g0044a0001c0003t0004g0045others(3): Show | 6 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-5171T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36981446 | ||||||
| chr17:36981449
|
C | CT | 12 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.833-5156dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36981449 | |||||
| chr17:36981528
|
C | T | 1 | a0001c0001t0007g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.833-5089C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36981528 | ||||||
| chr17:36981618
|
T | C | 29 | a0001c0001t0001g0147a0001c0001t0001g0242a0001c0001t0002g0001others(26): Show | 30 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.833-4999T>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36981618 | ||||||
| chr17:36981702
|
C | CT | 43 | a0001c0001t0001g0060a0001c0001t0001g0108a0001c0001t0001g0121others(40): Show | 44 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.833-4898dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36981702 | |||||
| chr17:36981702
|
C | CTT | 27 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(24): Show | 27 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.833-4899_833-4898d others(4): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36981702 | |||||
| chr17:36981705
|
T | TC | 3 | a0001c0001t0001g0081a0003c0005t0001g0093a0003c0005t0001g0095 | 3 | HG03098.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.833-4912_833-4911i others(3): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36981705 | ||||||
| chr17:36981707
|
T | TTC | 18 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(15): Show | 18 | HG01891.hp1 HG02135.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.833-4909_833-4908i others(4): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36981707 | |||||
| chr17:36981896
|
G | C | 1 | a0001c0003t0001g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.833-4721G>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36981896 | ||||||
| chr17:36982004
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.833-4613T>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36982004 | ||||||
| chr17:36982070
|
A | G | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-4547A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36982070 | ||||||
| chr17:36982233
|
G | GT | 9 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0218others(6): Show | 9 | HG01109.hp2 HG02486.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.833-4368dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36982233 | |||||
| chr17:36982233
|
GT | G | 72 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0024others(69): Show | 73 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.833-4368delT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36982233 | |||||
| chr17:36982233
|
GTT | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0033others(10): Show | 13 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.833-4369_833-4368d others(4): Show |
AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36982233 | |||||
| chr17:36982239
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0105 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.833-4378T>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36982239 | ||||||
| chr17:36982446
|
C | A | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.833-4171C>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36982446 | ||||||
| chr17:36982710
|
A | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02257.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.833-3907A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36982710 | ||||||
| chr17:36982926
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.833-3691A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36982926 | ||||||
| chr17:36983078
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.833-3539A>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36983078 | ||||||
| chr17:36983136
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.833-3481G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36983136 | ||||||
| chr17:36983616
|
GC | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.833-3000delC | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36983616 | ||||||
| chr17:36984188
|
G | A | 1 | a0001c0001t0007g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.833-2429G>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36984188 | ||||||
| chr17:36984239
|
G | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0218 | 2 | HG00558.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.833-2378G>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36984239 | ||||||
| chr17:36984366
|
C | A | 1 | a0001c0001t0002g0145 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.833-2251C>A | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36984366 | ||||||
| chr17:36984661
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.833-1956C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36984661 | ||||||
| chr17:36984811
|
A | C | 1 | a0001c0009t0001g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.833-1806A>C | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36984811 | ||||||
| chr17:36984901
|
G | GT | 35 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0081others(32): Show | 36 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.833-1698dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36984901 | |||||
| chr17:36984901
|
GT | G | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.833-1698delT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36984901 | |||||
| chr17:36984975
|
C | T | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.833-1642C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36984975 | ||||||
| chr17:36985110
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.833-1507C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36985110 | ||||||
| chr17:36985260
|
C | G | 6 | a0001c0001t0003g0016a0001c0001t0003g0075a0001c0001t0003g0076others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.833-1357C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36985260 | ||||||
| chr17:36985356
|
C | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG01192.hp2 HG01361.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-1261C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36985356 | ||||||
| chr17:36985380
|
C | G | 3 | a0001c0003t0001g0091a0002c0004t0001g0097a0002c0004t0001g0098 | 3 | HG02723.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.833-1237C>G | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36985380 | ||||||
| chr17:36985442
|
A | AT | 8 | a0001c0001t0001g0072a0001c0001t0002g0107a0001c0001t0002g0113others(5): Show | 8 | HG01361.hp1 HG02257.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.833-1156dupT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36985442 | |||||
| chr17:36985442
|
AT | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(14): Show | 17 | HG01891.hp1 HG02135.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.833-1156delT | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | 36985442 | |||||
| chr17:36985582
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0200 | 2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.833-1035C>T | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | chr17 | 36985582 | ||||||
| chr17:36985642
|
T | C | 90 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(87): Show |