Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2975 |
|---|---|
| ensemblid | ENSG00000077235.18 |
| hgncid | 4664 |
| symbol | GTF3C1 |
| name | general transcription factor IIIC subunit 1 |
| refseq_nuc | NM_001520.4 |
| refseq_prot | NP_001511.2 |
| ensembl_nuc | ENST00000356183.9 |
| ensembl_prot | ENSP00000348510.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 27460613 |
| end | 27549913 |
| strand | - |
| ver | v1.2 |
| region | chr16:27460613-27549913 |
| region5000 | chr16:27455613-27554913 |
| regionname0 | GTF3C1_chr16_27460613_27549913 |
| regionname5000 | GTF3C1_chr16_27455613_27554913 |
| 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 | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2109 | 193 | 71 | 35 | 68 | 6 | 11 | 49 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0002 | 0/0 | 2109 | 11 | 0 | 7 | 0 | 4 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0003 | 0/0 | 2109 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0004 | 0/0 | 2109 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0005 | 0/0 | 2109 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0006 | 0/0 | 2109 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0007 | 0/0 | 2109 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0008 | 0/0 | 2109 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0009 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0010 | 0/0 | 2109 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0011 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0012 | 0/0 | 2109 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0013 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 6330 | 172 | 59 | 31 | 63 | 6 | 11 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0002 | 0/0 | 6330 | 11 | 0 | 7 | 0 | 4 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0003 | 0/0 | 6330 | 5 | 5 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0004 | 0/0 | 6330 | 3 | 0 | 0 | 3 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0005 | 0/0 | 6330 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0006 | 0/0 | 6330 | 3 | 0 | 0 | 2 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0007 | 0/0 | 6330 | 3 | 2 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0008 | 0/0 | 6330 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0009 | 0/0 | 6330 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0010 | 0/0 | 6330 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0011 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0012 | 0/0 | 6330 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0013 | 0/0 | 6330 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0014 | 0/0 | 6330 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0015 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0016 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0017 | 0/0 | 6330 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0018 | 0/0 | 6330 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0019 | 0/0 | 6330 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0020 | 0/0 | 6330 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0021 | 0/0 | 6330 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0022 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0023 | 0/0 | 6330 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| c0024 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| thapid | grch38chm13v2 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 761 | 199 | 70 | 32 | 72 | 10 | 13 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| t0002 | 0/0 | 761 | 11 | 0 | 10 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| t0003 | 0/0 | 761 | 7 | 6 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| t0004 | 0/0 | 761 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| t0005 | 0/0 | 761 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| t0006 | 0/0 | 761 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| achapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 6330 | 172 | 59 | 31 | 63 | 6 | 11 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0003 | 0/0 | 6330 | 5 | 5 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0004 | 0/0 | 6330 | 3 | 0 | 0 | 3 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0007 | 0/0 | 6330 | 3 | 2 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0008 | 0/0 | 6330 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0009 | 0/0 | 6330 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0011 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0013 | 0/0 | 6330 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0019 | 0/0 | 6330 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0022 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0023 | 0/0 | 6330 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0024 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0002c0002 | 0/0 | 6330 | 11 | 0 | 7 | 0 | 4 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0003c0006 | 0/0 | 6330 | 3 | 0 | 0 | 2 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0004c0005 | 0/0 | 6330 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0005c0010 | 0/0 | 6330 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0006c0021 | 0/0 | 6330 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0007c0014 | 0/0 | 6330 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0008c0012 | 0/0 | 6330 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0009c0018 | 0/0 | 6330 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0010c0017 | 0/0 | 6330 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0011c0016 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0012c0015 | 0/0 | 6330 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0013c0020 | 0/0 | 6330 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7090 | 153 | 52 | 20 | 63 | 6 | 10 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0001t0002 | 0/0 | 7090 | 11 | 0 | 10 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0001t0003 | 0/0 | 7090 | 7 | 6 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0001t0005 | 0/0 | 7090 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0003t0001 | 0/0 | 7090 | 5 | 5 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0004t0001 | 0/0 | 7090 | 3 | 0 | 0 | 3 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0007t0001 | 0/0 | 7090 | 3 | 2 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0008t0001 | 0/0 | 7090 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0009t0001 | 0/0 | 7090 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0011t0001 | 0/0 | 7090 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0013t0001 | 0/0 | 7090 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0019t0001 | 0/0 | 7090 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0022t0004 | 0/0 | 7090 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0023t0001 | 0/0 | 7090 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0001c0024t0001 | 0/0 | 7090 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0002c0002t0001 | 0/0 | 7090 | 10 | 0 | 6 | 0 | 4 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0002c0002t0006 | 0/0 | 7090 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0003c0006t0001 | 0/0 | 7090 | 3 | 0 | 0 | 2 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0004c0005t0001 | 0/0 | 7090 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0005c0010t0001 | 0/0 | 7090 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0006c0021t0001 | 0/0 | 7090 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0007c0014t0001 | 0/0 | 7090 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0008c0012t0001 | 0/0 | 7090 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0009c0018t0001 | 0/0 | 7090 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0010c0017t0001 | 0/0 | 7090 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0011c0016t0001 | 0/0 | 7090 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0012c0015t0001 | 0/0 | 7090 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| a0013c0020t0001 | 0/0 | 7090 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | copy fasta | chr16 | 27455613 | 27554913 |
| actghapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0003g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0003t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0007t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0007t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0007t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0008t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0009t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0009t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0011t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0013t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0019t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0022t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0023t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0001c0024t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0002c0002t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0003c0006t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0003c0006t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0004c0005t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0004c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0005c0010t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0005c0010t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0006c0021t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0007c0014t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0008c0012t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0009c0018t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0010c0017t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0011c0016t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0012c0015t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| a0013c0020t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0080 | EUR | GBR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0073 | EUR | GBR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01081 | hp1 | a0007 | c0014 | t0001 | g0163 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01106 | hp2 | a0008 | c0012 | t0001 | g0030 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01168 | hp1 | a0001 | c0008 | t0001 | g0014 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01169 | hp2 | a0001 | c0008 | t0001 | g0014 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01175 | hp2 | a0001 | c0023 | t0001 | g0150 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01243 | hp1 | a0001 | c0007 | t0001 | g0040 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0074 | EUR | IBS | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0072 | EUR | IBS | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01891 | hp1 | a0005 | c0010 | t0001 | g0183 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01952 | hp1 | a0002 | c0002 | t0006 | g0081 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0066 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02165 | hp2 | a0001 | c0013 | t0001 | g0109 | EAS | CDX | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02280 | hp1 | a0001 | c0022 | t0004 | g0021 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02572 | hp2 | a0001 | c0011 | t0001 | g0100 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02647 | hp2 | a0004 | c0005 | t0001 | g0008 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02683 | hp1 | a0006 | c0021 | t0001 | g0079 | SAS | PJL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0029 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02809 | hp2 | a0004 | c0005 | t0001 | g0008 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02818 | hp1 | a0001 | c0007 | t0001 | g0039 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02896 | hp1 | a0004 | c0005 | t0001 | g0047 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03486 | hp1 | a0005 | c0010 | t0001 | g0170 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03486 | hp2 | a0001 | c0009 | t0001 | g0155 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03834 | hp2 | a0003 | c0006 | t0001 | g0016 | SAS | BEB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG04204 | hp1 | a0010 | c0017 | t0001 | g0134 | SAS | STU | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18612 | hp1 | a0013 | c0020 | t0001 | g0173 | EAS | CHB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | YRI | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0023 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18960 | hp2 | a0003 | c0006 | t0001 | g0016 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18999 | hp1 | a0001 | c0004 | t0001 | g0022 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19043 | hp1 | a0001 | c0009 | t0001 | g0185 | AFR | LWK | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | LWK | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19068 | hp2 | a0009 | c0018 | t0001 | g0112 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19091 | hp1 | a0001 | c0019 | t0001 | g0085 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19091 | hp2 | a0003 | c0006 | t0001 | g0125 | EAS | JPT | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ASW | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02486 | hp1 | a0001 | c0024 | t0001 | g0193 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA21309 | hp1 | a0011 | c0016 | t0001 | g0141 | AFR | LWK | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| NA21309 | hp2 | a0012 | c0015 | t0001 | g0077 | AFR | LWK | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0117 | REF | REF | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0076 | REF | REF | GTF3C1_chr16_27455613_27554913 | GTF3C1 | chr16 | 27455613 | 27554913 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:27461451
|
C | T | 4 | a0002a0006a0011others(1): Show | 14 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(11): Show |
missense_variant | MODERATE | c.6229G>A | p.Glu2077Lys | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 37/37 | 6252/7090 | 6229/6330 | 2077/2109 | chr16 | 27461451 | ||
| chr16:27463589
|
A | G | 3 | a0002a0006a0012 | 13 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(10): Show |
missense_variant | MODERATE | c.5876T>C | p.Phe1959Ser | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/37 | 5899/7090 | 5876/6330 | 1959/2109 | chr16 | 27463589 | ||
| chr16:27464494
|
C | T | 1 | a0003 | 3 | HG03834.hp2 NA18960.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.5698G>A | p.Gly1900Arg | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/37 | 5721/7090 | 5698/6330 | 1900/2109 | chr16 | 27464494 | ||
| chr16:27464508
|
G | A | 1 | a0010 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.5684C>T | p.Pro1895Leu | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/37 | 5707/7090 | 5684/6330 | 1895/2109 | chr16 | 27464508 | ||
| chr16:27464527
|
G | C | 1 | a0005 | 2 | HG01891.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.5665C>G | p.Gln1889Glu | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/37 | 5688/7090 | 5665/6330 | 1889/2109 | chr16 | 27464527 | ||
| chr16:27464569
|
C | T | 1 | a0012 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.5623G>A | p.Ala1875Thr | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/37 | 5646/7090 | 5623/6330 | 1875/2109 | chr16 | 27464569 | ||
| chr16:27464620
|
G | C | 1 | a0004 | 3 | HG02647.hp2 HG02809.hp2 HG02896.hp1 |
missense_variant | MODERATE | c.5572C>G | p.Arg1858Gly | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/37 | 5595/7090 | 5572/6330 | 1858/2109 | chr16 | 27464620 | ||
| chr16:27464652
|
G | A | 1 | a0009 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.5540C>T | p.Pro1847Leu | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/37 | 5563/7090 | 5540/6330 | 1847/2109 | chr16 | 27464652 | ||
| chr16:27465328
|
G | A | 1 | a0008 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.5287C>T | p.Arg1763Cys | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 33/37 | 5310/7090 | 5287/6330 | 1763/2109 | chr16 | 27465328 | ||
| chr16:27469476
|
C | T | 1 | a0007 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.4889G>A | p.Arg1630His | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/37 | 4912/7090 | 4889/6330 | 1630/2109 | chr16 | 27469476 | ||
| chr16:27489695
|
C | A | 1 | a0013 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.3200G>T | p.Gly1067Val | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 20/37 | 3223/7090 | 3200/6330 | 1067/2109 | chr16 | 27489695 | ||
| chr16:27492699
|
G | A | 1 | a0006 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.2891C>T | p.Ser964Leu | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 18/37 | 2914/7090 | 2891/6330 | 964/2109 | chr16 | 27492699 | ||
| chr16:27495273
|
G | A | 1 | a0003 | 3 | HG03834.hp2 NA18960.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.2570C>T | p.Pro857Leu | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 15/37 | 2593/7090 | 2570/6330 | 857/2109 | chr16 | 27495273 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:27470323
|
G | A | 1 | a0001c0019 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.4599C>T | p.Ala1533Ala | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 31/37 | 4622/7090 | 4599/6330 | 1533/2109 | chr16 | 27470323 | ||
| chr16:27488270
|
C | T | 1 | a0001c0013 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.3657G>A | p.Arg1219Arg | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/37 | 3680/7090 | 3657/6330 | 1219/2109 | chr16 | 27488270 | ||
| chr16:27488396
|
A | G | 1 | a0008c0012 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.3531T>C | p.Ile1177Ile | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/37 | 3554/7090 | 3531/6330 | 1177/2109 | chr16 | 27488396 | ||
| chr16:27488579
|
C | T | 1 | a0001c0022 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.3486G>A | p.Lys1162Lys | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 22/37 | 3509/7090 | 3486/6330 | 1162/2109 | chr16 | 27488579 | ||
| chr16:27492489
|
T | A | 1 | a0001c0003 | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
synonymous_variant | LOW | c.3000A>T | p.Ala1000Ala | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/37 | 3023/7090 | 3000/6330 | 1000/2109 | chr16 | 27492489 | ||
| chr16:27494823
|
G | A | 1 | a0001c0008 | 2 | HG01168.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.2718C>T | p.Ser906Ser | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/37 | 2741/7090 | 2718/6330 | 906/2109 | chr16 | 27494823 | ||
| chr16:27494847
|
G | A | 1 | a0001c0009 | 2 | HG03486.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.2694C>T | p.Phe898Phe | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/37 | 2717/7090 | 2694/6330 | 898/2109 | chr16 | 27494847 | ||
| chr16:27498727
|
G | A | 1 | a0001c0022 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.2068C>T | p.Leu690Leu | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 13/37 | 2091/7090 | 2068/6330 | 690/2109 | chr16 | 27498727 | ||
| chr16:27505926
|
G | A | 1 | a0001c0023 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1743C>T | p.Ile581Ile | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/37 | 1766/7090 | 1743/6330 | 581/2109 | chr16 | 27505926 | ||
| chr16:27506884
|
C | T | 1 | a0001c0011 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1515G>A | p.Arg505Arg | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 9/37 | 1538/7090 | 1515/6330 | 505/2109 | chr16 | 27506884 | ||
| chr16:27508575
|
G | A | 1 | a0005c0010 | 2 | HG01891.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.1207C>T | p.Leu403Leu | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/37 | 1230/7090 | 1207/6330 | 403/2109 | chr16 | 27508575 | ||
| chr16:27533333
|
C | A | 1 | a0001c0007 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
synonymous_variant | LOW | c.807G>T | p.Arg269Arg | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/37 | 830/7090 | 807/6330 | 269/2109 | chr16 | 27533333 | ||
| chr16:27549810
|
C | A | 1 | a0001c0024 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.81G>T | p.Arg27Arg | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/37 | 104/7090 | 81/6330 | 27/2109 | chr16 | 27549810 | ||
| chr16:27549879
|
C | T | 1 | a0001c0004 | 3 | NA18952.hp2 NA18999.hp1 NA19010.hp2 |
synonymous_variant | LOW | c.12G>A | p.Leu4Leu | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/37 | 35/7090 | 12/6330 | 4/2109 | chr16 | 27549879 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:27460657
|
A | G | 1 | a0001c0001t0002 | 11 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*693T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 37/37 | 693 | chr16 | 27460657 | |||||
| chr16:27460663
|
A | C | 1 | a0001c0001t0003 | 7 | HG01109.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*687T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 37/37 | 687 | chr16 | 27460663 | |||||
| chr16:27460837
|
C | T | 1 | a0002c0002t0006 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*513G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 37/37 | 513 | chr16 | 27460837 | |||||
| chr16:27460936
|
C | T | 2 | a0001c0001t0005a0001c0022t0004 | 2 | HG02055.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 37/37 | 414 | chr16 | 27460936 | |||||
| chr16:27549907
|
G | T | 1 | a0001c0022t0004 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/37 | 17 | chr16 | 27549907 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:27461949
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0082others(3): Show | 9 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.6117+345G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 36/36 | chr16 | 27461949 | ||||||
| chr16:27461988
|
C | T | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.6117+306G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 36/36 | chr16 | 27461988 | ||||||
| chr16:27462024
|
G | A | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.6117+270C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 36/36 | chr16 | 27462024 | ||||||
| chr16:27462041
|
A | T | 2 | a0005c0010t0001g0170a0005c0010t0001g0183 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.6117+253T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 36/36 | chr16 | 27462041 | ||||||
| chr16:27462079
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0013 | 7 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.6117+215C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 36/36 | chr16 | 27462079 | ||||||
| chr16:27462102
|
T | C | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.6117+192A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 36/36 | chr16 | 27462102 | ||||||
| chr16:27462257
|
G | A | 1 | a0010c0017t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6117+37C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 36/36 | chr16 | 27462257 | ||||||
| chr16:27462539
|
G | A | 13 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.5925-53C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27462539 | ||||||
| chr16:27462651
|
T | C | 2 | a0001c0001t0003g0006a0001c0001t0003g0031 | 3 | HG02145.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5925-165A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27462651 | ||||||
| chr16:27462698
|
T | C | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.5925-212A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27462698 | ||||||
| chr16:27462847
|
G | A | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 29 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.5925-361C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27462847 | ||||||
| chr16:27462893
|
A | G | 35 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(32): Show | 41 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.5925-407T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27462893 | ||||||
| chr16:27463074
|
T | A | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.5924+467A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27463074 | ||||||
| chr16:27463142
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5924+399C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27463142 | ||||||
| chr16:27463166
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0041 | 8 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.5924+375C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27463166 | ||||||
| chr16:27463308
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5924+233T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27463308 | ||||||
| chr16:27463492
|
C | T | 1 | a0010c0017t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5924+49G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 35/36 | chr16 | 27463492 | ||||||
| chr16:27464056
|
G | A | 1 | a0001c0001t0001g0012 | 2 | NA18962.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.5872+264C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/36 | chr16 | 27464056 | ||||||
| chr16:27464068
|
C | A | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.5872+252G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/36 | chr16 | 27464068 | ||||||
| chr16:27464159
|
T | A | 1 | a0006c0021t0001g0079 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5872+161A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/36 | chr16 | 27464159 | ||||||
| chr16:27464239
|
G | C | 8 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(5): Show | 8 | HG01258.hp1 HG01261.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.5872+81C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/36 | chr16 | 27464239 | ||||||
| chr16:27464285
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0013 | 7 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5872+35C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/36 | chr16 | 27464285 | ||||||
| chr16:27464299
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5872+21C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 34/36 | chr16 | 27464299 | ||||||
| chr16:27464978
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(35): Show | 49 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.5356-142A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 33/36 | chr16 | 27464978 | ||||||
| chr16:27465011
|
C | T | 1 | a0001c0008t0001g0014 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.5356-175G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 33/36 | chr16 | 27465011 | ||||||
| chr16:27465227
|
G | A | 36 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(33): Show | 42 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.5355+33C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 33/36 | chr16 | 27465227 | ||||||
| chr16:27465575
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5075-35C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27465575 | ||||||
| chr16:27465919
|
T | G | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5075-379A>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27465919 | ||||||
| chr16:27465996
|
G | A | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.5075-456C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27465996 | ||||||
| chr16:27466004
|
A | T | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.5075-464T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27466004 | ||||||
| chr16:27466083
|
C | CCAGA | 36 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(33): Show | 42 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.5075-544_5075-543i others(6): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27466083 | ||||||
| chr16:27466281
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5075-741G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27466281 | ||||||
| chr16:27466434
|
CAT | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0013 | 7 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5075-896_5075-895d others(4): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27466434 | ||||||
| chr16:27466508
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(189): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.5075-968T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27466508 | ||||||
| chr16:27466981
|
G | A | 1 | a0001c0007t0001g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5075-1441C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27466981 | ||||||
| chr16:27467304
|
G | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5075-1764C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27467304 | ||||||
| chr16:27467324
|
C | T | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.5075-1784G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27467324 | ||||||
| chr16:27467829
|
C | T | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5074+1462G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27467829 | ||||||
| chr16:27467908
|
T | C | 13 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.5074+1383A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27467908 | ||||||
| chr16:27468099
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.5074+1192G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468099 | ||||||
| chr16:27468310
|
A | G | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.5074+981T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468310 | ||||||
| chr16:27468446
|
T | C | 13 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.5074+845A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468446 | ||||||
| chr16:27468457
|
A | T | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5074+834T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468457 | ||||||
| chr16:27468642
|
A | C | 1 | a0002c0002t0001g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5074+649T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468642 | ||||||
| chr16:27468725
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5074+566G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468725 | ||||||
| chr16:27468807
|
T | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(30): Show | 39 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.5074+484A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468807 | ||||||
| chr16:27468935
|
G | A | 1 | a0010c0017t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5074+356C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468935 | ||||||
| chr16:27468948
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0013 | 7 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5074+343G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468948 | ||||||
| chr16:27468966
|
C | T | 2 | a0005c0010t0001g0170a0005c0010t0001g0183 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5074+325G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468966 | ||||||
| chr16:27468981
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5074+310G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27468981 | ||||||
| chr16:27469052
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 6 | HG02970.hp2 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.5074+239G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 32/36 | chr16 | 27469052 | ||||||
| chr16:27469677
|
A | C | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4815-127T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 31/36 | chr16 | 27469677 | ||||||
| chr16:27469814
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4815-264G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 31/36 | chr16 | 27469814 | ||||||
| chr16:27469863
|
T | A | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4814+245A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 31/36 | chr16 | 27469863 | ||||||
| chr16:27469896
|
C | T | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4814+212G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 31/36 | chr16 | 27469896 | ||||||
| chr16:27469907
|
G | A | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4814+201C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 31/36 | chr16 | 27469907 | ||||||
| chr16:27469929
|
C | T | 9 | a0001c0001t0001g0019a0001c0001t0001g0114a0001c0001t0001g0140others(6): Show | 10 | HG01081.hp1 HG01258.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.4814+179G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 31/36 | chr16 | 27469929 | ||||||
| chr16:27470472
|
G | A | 1 | a0001c0001t0001g0013 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4527-77C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27470472 | ||||||
| chr16:27470515
|
T | C | 36 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(33): Show | 42 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.4527-120A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27470515 | ||||||
| chr16:27470677
|
G | T | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4527-282C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27470677 | ||||||
| chr16:27470704
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4527-309G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27470704 | ||||||
| chr16:27471161
|
G | C | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4526+587C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27471161 | ||||||
| chr16:27471229
|
G | A | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4526+519C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27471229 | ||||||
| chr16:27471265
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0013 | 7 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4526+483C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27471265 | ||||||
| chr16:27471404
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4526+344G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27471404 | ||||||
| chr16:27471581
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4526+167C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27471581 | ||||||
| chr16:27471640
|
G | A | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4526+108C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 30/36 | chr16 | 27471640 | ||||||
| chr16:27471935
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4354-15C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27471935 | ||||||
| chr16:27471937
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4354-17G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27471937 | ||||||
| chr16:27472015
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4354-95A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27472015 | ||||||
| chr16:27472028
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4354-108G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27472028 | ||||||
| chr16:27472209
|
C | T | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4354-289G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27472209 | ||||||
| chr16:27472325
|
A | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0139a0001c0004t0001g0022others(1): Show | 4 | NA18952.hp2 NA18999.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.4354-405T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27472325 | ||||||
| chr16:27472558
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.4354-638G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27472558 | ||||||
| chr16:27472623
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4354-703G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27472623 | ||||||
| chr16:27472656
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0013 | 7 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4354-736C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27472656 | ||||||
| chr16:27472896
|
G | A | 1 | a0010c0017t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4354-976C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27472896 | ||||||
| chr16:27472967
|
A | C | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4354-1047T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27472967 | ||||||
| chr16:27473321
|
A | G | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4354-1401T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27473321 | ||||||
| chr16:27473519
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4354-1599T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27473519 | ||||||
| chr16:27473675
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4354-1755C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27473675 | ||||||
| chr16:27473937
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0013 | 7 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4354-2017A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27473937 | ||||||
| chr16:27473997
|
G | C | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4354-2077C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27473997 | ||||||
| chr16:27474038
|
C | T | 1 | a0013c0020t0001g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4354-2118G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27474038 | ||||||
| chr16:27474493
|
A | T | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4353+1958T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27474493 | ||||||
| chr16:27474700
|
C | G | 17 | a0001c0001t0001g0119a0001c0001t0001g0131a0001c0001t0001g0132others(14): Show | 17 | HG00741.hp1 HG01099.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.4353+1751G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27474700 | ||||||
| chr16:27474724
|
CA | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4353+1726delT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27474724 | ||||||
| chr16:27474820
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4353+1631T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27474820 | ||||||
| chr16:27474905
|
C | A | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4353+1546G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27474905 | ||||||
| chr16:27474930
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0152 | 2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4353+1521C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27474930 | ||||||
| chr16:27475047
|
C | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 6 | NA18967.hp2 NA18993.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.4353+1404G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27475047 | ||||||
| chr16:27475248
|
A | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(65): Show | 84 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.4353+1203T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27475248 | ||||||
| chr16:27475338
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4353+1113G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27475338 | ||||||
| chr16:27475491
|
G | A | 1 | a0001c0004t0001g0024 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4353+960C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27475491 | ||||||
| chr16:27475698
|
T | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4353+753A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27475698 | ||||||
| chr16:27476365
|
C | T | 4 | a0001c0001t0002g0004a0001c0001t0002g0171a0001c0001t0002g0172others(1): Show | 6 | HG01123.hp1 HG01358.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.4353+86G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 29/36 | chr16 | 27476365 | ||||||
| chr16:27476654
|
C | T | 1 | a0001c0003t0001g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4260-110G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27476654 | ||||||
| chr16:27476749
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4260-205T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27476749 | ||||||
| chr16:27476873
|
C | T | 32 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(29): Show | 38 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.4260-329G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27476873 | ||||||
| chr16:27476947
|
G | T | 1 | a0001c0001t0001g0165 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.4260-403C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27476947 | ||||||
| chr16:27477201
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4260-657G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27477201 | ||||||
| chr16:27477202
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4260-658G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27477202 | ||||||
| chr16:27477417
|
C | T | 18 | a0001c0001t0001g0087a0001c0001t0001g0121a0001c0001t0001g0174others(15): Show | 21 | HG00099.hp1 HG00639.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.4260-873G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27477417 | ||||||
| chr16:27477497
|
G | A | 2 | a0001c0001t0005g0066a0001c0022t0004g0021 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4260-953C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27477497 | ||||||
| chr16:27477551
|
G | A | 32 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(29): Show | 38 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.4259+918C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27477551 | ||||||
| chr16:27477648
|
G | T | 2 | a0005c0010t0001g0170a0005c0010t0001g0183 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4259+821C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27477648 | ||||||
| chr16:27477987
|
C | T | 23 | a0001c0001t0001g0087a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 26 | HG00099.hp1 HG00639.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.4259+482G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27477987 | ||||||
| chr16:27478437
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4259+32C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 28/36 | chr16 | 27478437 | ||||||
| chr16:27478645
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4197-114C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27478645 | ||||||
| chr16:27478895
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4197-364C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27478895 | ||||||
| chr16:27479318
|
AT | A | 32 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(29): Show | 38 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.4197-788delA | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27479318 | ||||||
| chr16:27479446
|
G | A | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4197-915C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27479446 | ||||||
| chr16:27479777
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4197-1246T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27479777 | ||||||
| chr16:27479826
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4196+1253A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27479826 | ||||||
| chr16:27479935
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4196+1144A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27479935 | ||||||
| chr16:27480008
|
G | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4196+1071C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480008 | ||||||
| chr16:27480184
|
G | A | 2 | a0001c0001t0001g0162a0007c0014t0001g0163 | 2 | HG01081.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.4196+895C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480184 | ||||||
| chr16:27480201
|
C | CA | 5 | a0001c0001t0001g0095a0001c0001t0001g0138a0001c0001t0001g0149others(2): Show | 5 | HG00639.hp1 HG01175.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.4196+877dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480201 | ||||||
| chr16:27480201
|
CA | C | 28 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0092others(25): Show | 33 | HG00099.hp2 HG00140.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.4196+877delT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480201 | ||||||
| chr16:27480201
|
CAAA | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 7 | HG02109.hp2 HG02970.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.4196+875_4196+877d others(5): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480201 | ||||||
| chr16:27480294
|
G | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0171a0001c0001t0002g0172others(1): Show | 6 | HG01123.hp1 HG01358.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.4196+785C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480294 | ||||||
| chr16:27480544
|
G | T | 5 | a0001c0001t0001g0121a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 5 | HG01071.hp2 HG02300.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.4196+535C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480544 | ||||||
| chr16:27480668
|
G | A | 13 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4196+411C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480668 | ||||||
| chr16:27480709
|
T | C | 35 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(32): Show | 41 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.4196+370A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480709 | ||||||
| chr16:27480713
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4196+366C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480713 | ||||||
| chr16:27480881
|
C | T | 3 | a0001c0001t0005g0066a0001c0007t0001g0029a0001c0022t0004g0021 | 3 | HG02055.hp2 HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.4196+198G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27480881 | ||||||
| chr16:27481046
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4196+33C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27481046 | ||||||
| chr16:27481055
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4196+24C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 27/36 | chr16 | 27481055 | ||||||
| chr16:27481343
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4084-152C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 26/36 | chr16 | 27481343 | ||||||
| chr16:27481705
|
T | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 16 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.4084-514A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 26/36 | chr16 | 27481705 | ||||||
| chr16:27481755
|
G | A | 2 | a0001c0001t0003g0002a0001c0001t0003g0006 | 6 | HG01109.hp1 HG02145.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.4084-564C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 26/36 | chr16 | 27481755 | ||||||
| chr16:27481790
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4084-599C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 26/36 | chr16 | 27481790 | ||||||
| chr16:27482063
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4084-872C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 26/36 | chr16 | 27482063 | ||||||
| chr16:27482086
|
G | A | 2 | a0001c0007t0001g0039a0001c0007t0001g0040 | 2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4084-895C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 26/36 | chr16 | 27482086 | ||||||
| chr16:27482204
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 15 | HG01109.hp1 HG02145.hp1 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.4083+840G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 26/36 | chr16 | 27482204 | ||||||
| chr16:27482408
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4083+636C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 26/36 | chr16 | 27482408 | ||||||
| chr16:27482678
|
TCAG | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0153 | 3 | HG00639.hp1 HG01169.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.4083+363_4083+365d others(5): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 26/36 | chr16 | 27482678 | ||||||
| chr16:27483128
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02155.hp2 | splice_region_variant&intron_variant | LOW | c.4002-3C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 25/36 | chr16 | 27483128 | ||||||
| chr16:27483354
|
C | T | 31 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(28): Show | 37 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.4002-229G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 25/36 | chr16 | 27483354 | ||||||
| chr16:27483556
|
A | C | 22 | a0001c0001t0001g0067a0001c0001t0001g0115a0001c0001t0001g0122others(19): Show | 23 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.4002-431T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 25/36 | chr16 | 27483556 | ||||||
| chr16:27483972
|
C | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(32): Show | 46 | HG00099.hp2 HG00140.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.4001+239G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 25/36 | chr16 | 27483972 | ||||||
| chr16:27484105
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4001+106G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 25/36 | chr16 | 27484105 | ||||||
| chr16:27484162
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4001+49C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 25/36 | chr16 | 27484162 | ||||||
| chr16:27484176
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4001+35C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 25/36 | chr16 | 27484176 | ||||||
| chr16:27484535
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3859-182C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27484535 | ||||||
| chr16:27484620
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3859-267G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27484620 | ||||||
| chr16:27484634
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3859-281T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27484634 | ||||||
| chr16:27484702
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0013 | 7 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3859-349C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27484702 | ||||||
| chr16:27484852
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3859-499C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27484852 | ||||||
| chr16:27484957
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3859-604A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27484957 | ||||||
| chr16:27485426
|
G | A | 3 | a0001c0001t0001g0119a0001c0004t0001g0022a0001c0004t0001g0023 | 3 | NA18952.hp2 NA18999.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3858+571C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27485426 | ||||||
| chr16:27485664
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3858+333C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27485664 | ||||||
| chr16:27485790
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3858+207G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27485790 | ||||||
| chr16:27485955
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3858+42C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27485955 | ||||||
| chr16:27485969
|
C | G | 1 | a0001c0008t0001g0014 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3858+28G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 24/36 | chr16 | 27485969 | ||||||
| chr16:27486236
|
C | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3701-82G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27486236 | ||||||
| chr16:27486337
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3701-183A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27486337 | ||||||
| chr16:27486496
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3701-342C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27486496 | ||||||
| chr16:27486497
|
C | T | 1 | a0001c0004t0001g0024 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3701-343G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27486497 | ||||||
| chr16:27486583
|
G | A | 4 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040others(1): Show | 4 | HG01106.hp2 HG01243.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3701-429C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27486583 | ||||||
| chr16:27486722
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0120a0001c0001t0001g0146others(2): Show | 6 | HG01515.hp2 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3701-568C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27486722 | ||||||
| chr16:27486986
|
C | T | 1 | a0010c0017t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3701-832G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27486986 | ||||||
| chr16:27487057
|
T | C | 1 | a0001c0001t0001g0017 | 2 | HG01515.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3701-903A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27487057 | ||||||
| chr16:27487412
|
T | A | 33 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(30): Show | 39 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3700+815A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27487412 | ||||||
| chr16:27487432
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3700+795A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27487432 | ||||||
| chr16:27487632
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 9 | HG02896.hp2 HG02970.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.3700+595T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27487632 | ||||||
| chr16:27487654
|
G | A | 1 | a0011c0016t0001g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3700+573C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27487654 | ||||||
| chr16:27487695
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0160 | 3 | HG02055.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3700+532T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27487695 | ||||||
| chr16:27488027
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3700+200G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27488027 | ||||||
| chr16:27488028
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3700+199C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27488028 | ||||||
| chr16:27488040
|
T | G | 34 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(31): Show | 40 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3700+187A>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27488040 | ||||||
| chr16:27488060
|
G | C | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3700+167C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27488060 | ||||||
| chr16:27488078
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.3700+149G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27488078 | ||||||
| chr16:27488168
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0161a0001c0001t0001g0168 | 4 | HG02572.hp1 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3700+59G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 23/36 | chr16 | 27488168 | ||||||
| chr16:27488712
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(63): Show | 82 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.3430-77C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 21/36 | chr16 | 27488712 | ||||||
| chr16:27488741
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3430-106A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 21/36 | chr16 | 27488741 | ||||||
| chr16:27488873
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3429+170C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 21/36 | chr16 | 27488873 | ||||||
| chr16:27488911
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3429+132G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 21/36 | chr16 | 27488911 | ||||||
| chr16:27489268
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3294-90A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 20/36 | chr16 | 27489268 | ||||||
| chr16:27489320
|
T | C | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3294-142A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 20/36 | chr16 | 27489320 | ||||||
| chr16:27489386
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3294-208A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 20/36 | chr16 | 27489386 | ||||||
| chr16:27489457
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3293+145A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 20/36 | chr16 | 27489457 | ||||||
| chr16:27489497
|
G | A | 1 | a0011c0016t0001g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3293+105C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 20/36 | chr16 | 27489497 | ||||||
| chr16:27489775
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3152-32G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27489775 | ||||||
| chr16:27489868
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0041others(2): Show | 10 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.3152-125G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27489868 | ||||||
| chr16:27489868
|
C | T | 31 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(28): Show | 37 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.3152-125G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27489868 | ||||||
| chr16:27489933
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3152-190C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27489933 | ||||||
| chr16:27490302
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3152-559G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27490302 | ||||||
| chr16:27490595
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3152-852T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27490595 | ||||||
| chr16:27491053
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3151+1285C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27491053 | ||||||
| chr16:27491054
|
C | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3151+1284G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27491054 | ||||||
| chr16:27491100
|
A | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(31): Show | 40 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.3151+1238T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27491100 | ||||||
| chr16:27491217
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3151+1121C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27491217 | ||||||
| chr16:27491424
|
G | A | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3151+914C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27491424 | ||||||
| chr16:27491439
|
A | G | 26 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 30 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.3151+899T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27491439 | ||||||
| chr16:27491734
|
CG | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(79): Show | 98 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.3151+603delC | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27491734 | ||||||
| chr16:27491956
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0189 | 3 | HG01081.hp2 HG01099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.3151+382G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27491956 | ||||||
| chr16:27492014
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3151+324G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27492014 | ||||||
| chr16:27492065
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3151+273G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27492065 | ||||||
| chr16:27492078
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3151+260T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27492078 | ||||||
| chr16:27492319
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 10 | HG02109.hp2 HG02896.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.3151+19G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 19/36 | chr16 | 27492319 | ||||||
| chr16:27492733
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2877-20C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 17/36 | chr16 | 27492733 | ||||||
| chr16:27492906
|
G | A | 2 | a0005c0010t0001g0170a0005c0010t0001g0183 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2877-193C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 17/36 | chr16 | 27492906 | ||||||
| chr16:27493188
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2876+11T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 17/36 | chr16 | 27493188 | ||||||
| chr16:27493565
|
G | A | 6 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG00140.hp1 HG00639.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.2779-269C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27493565 | ||||||
| chr16:27493571
|
A | G | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2779-275T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27493571 | ||||||
| chr16:27493755
|
G | T | 2 | a0004c0005t0001g0008a0004c0005t0001g0047 | 3 | HG02647.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2779-459C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27493755 | ||||||
| chr16:27493797
|
T | C | 2 | a0001c0001t0001g0162a0007c0014t0001g0163 | 2 | HG01081.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2779-501A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27493797 | ||||||
| chr16:27493877
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2779-581G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27493877 | ||||||
| chr16:27493931
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2779-635G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27493931 | ||||||
| chr16:27493931
|
CT | C | 13 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2779-636delA | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27493931 | ||||||
| chr16:27494070
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2778+693A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494070 | ||||||
| chr16:27494184
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(66): Show | 85 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.2778+579T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494184 | ||||||
| chr16:27494236
|
T | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(66): Show | 85 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.2778+527A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494236 | ||||||
| chr16:27494278
|
G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0153 | 3 | HG00639.hp1 HG01169.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2778+485C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494278 | ||||||
| chr16:27494355
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2778+408G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494355 | ||||||
| chr16:27494380
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2778+383C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494380 | ||||||
| chr16:27494402
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2778+348_2778+360d others(15): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494402 | ||||||
| chr16:27494413
|
C | CA | 8 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0049others(5): Show | 13 | HG00140.hp2 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2778+349dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494413 | ||||||
| chr16:27494493
|
A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 10 | HG02109.hp2 HG02896.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2778+270T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494493 | ||||||
| chr16:27494526
|
G | A | 1 | a0001c0001t0002g0020 | 2 | HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.2778+237C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494526 | ||||||
| chr16:27494554
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2778+209A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494554 | ||||||
| chr16:27494578
|
T | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 10 | HG02109.hp2 HG02896.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.2778+185A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 16/36 | chr16 | 27494578 | ||||||
| chr16:27495118
|
G | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2632+93C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 15/36 | chr16 | 27495118 | ||||||
| chr16:27495504
|
G | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(31): Show | 40 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.2351-12C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27495504 | ||||||
| chr16:27496016
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2351-524C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27496016 | ||||||
| chr16:27496065
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2351-573C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27496065 | ||||||
| chr16:27496197
|
G | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2351-705C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27496197 | ||||||
| chr16:27496241
|
C | T | 15 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0091others(12): Show | 15 | HG00408.hp2 HG00423.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.2351-749G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27496241 | ||||||
| chr16:27496309
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2351-817A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27496309 | ||||||
| chr16:27496876
|
A | G | 2 | a0005c0010t0001g0170a0005c0010t0001g0183 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2350+761T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27496876 | ||||||
| chr16:27496899
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2350+738A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27496899 | ||||||
| chr16:27496998
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0160 | 3 | HG02055.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2350+639A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27496998 | ||||||
| chr16:27497183
|
G | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 5 | HG00408.hp1 NA18747.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2350+454C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27497183 | ||||||
| chr16:27497238
|
A | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2350+399T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27497238 | ||||||
| chr16:27497494
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2350+143C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27497494 | ||||||
| chr16:27497560
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2350+77C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 14/36 | chr16 | 27497560 | ||||||
| chr16:27497893
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2166-72C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 13/36 | chr16 | 27497893 | ||||||
| chr16:27498243
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2165+387G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 13/36 | chr16 | 27498243 | ||||||
| chr16:27498403
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2165+227C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 13/36 | chr16 | 27498403 | ||||||
| chr16:27498613
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2165+17G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 13/36 | chr16 | 27498613 | ||||||
| chr16:27498796
|
C | CA | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(153): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2062-64dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27498796 | ||||||
| chr16:27498884
|
C | G | 2 | a0001c0001t0003g0006a0001c0022t0004g0021 | 3 | HG02145.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2062-151G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27498884 | ||||||
| chr16:27499037
|
G | A | 2 | a0005c0010t0001g0170a0005c0010t0001g0183 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2062-304C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27499037 | ||||||
| chr16:27499133
|
T | A | 2 | a0001c0001t0003g0006a0001c0022t0004g0021 | 3 | HG02145.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2062-400A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27499133 | ||||||
| chr16:27499162
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2062-429G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27499162 | ||||||
| chr16:27499206
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2062-473G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27499206 | ||||||
| chr16:27499338
|
G | A | 1 | a0001c0001t0002g0020 | 2 | HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.2062-605C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27499338 | ||||||
| chr16:27499473
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2062-740C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27499473 | ||||||
| chr16:27499489
|
G | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0120others(2): Show | 10 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2062-756C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27499489 | ||||||
| chr16:27499620
|
A | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0107 | 3 | NA18941.hp2 NA18999.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2062-887T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27499620 | ||||||
| chr16:27499949
|
G | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 28 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.2062-1216C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27499949 | ||||||
| chr16:27500090
|
G | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 28 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.2061+1101C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500090 | ||||||
| chr16:27500135
|
G | A | 1 | a0002c0002t0001g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2061+1056C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500135 | ||||||
| chr16:27500157
|
C | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2061+1034G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500157 | ||||||
| chr16:27500243
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0061 | 3 | NA18967.hp2 NA18993.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2061+948C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500243 | ||||||
| chr16:27500309
|
G | A | 4 | a0001c0001t0002g0004a0001c0001t0002g0171a0001c0001t0002g0172others(1): Show | 6 | HG01123.hp1 HG01358.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2061+882C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500309 | ||||||
| chr16:27500349
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2061+842G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500349 | ||||||
| chr16:27500774
|
C | T | 1 | a0011c0016t0001g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2061+417G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500774 | ||||||
| chr16:27500775
|
G | A | 2 | a0004c0005t0001g0008a0004c0005t0001g0047 | 3 | HG02647.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2061+416C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500775 | ||||||
| chr16:27500781
|
G | A | 2 | a0004c0005t0001g0008a0004c0005t0001g0047 | 3 | HG02647.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2061+410C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500781 | ||||||
| chr16:27500955
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2061+236T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27500955 | ||||||
| chr16:27501021
|
T | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG01109.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2061+170A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 12/36 | chr16 | 27501021 | ||||||
| chr16:27501399
|
C | T | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1908-55G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 11/36 | chr16 | 27501399 | ||||||
| chr16:27501439
|
T | C | 13 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1908-95A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 11/36 | chr16 | 27501439 | ||||||
| chr16:27501439
|
T | G | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1908-95A>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 11/36 | chr16 | 27501439 | ||||||
| chr16:27501900
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1908-556G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 11/36 | chr16 | 27501900 | ||||||
| chr16:27502078
|
A | G | 1 | a0001c0019t0001g0085 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1908-734T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 11/36 | chr16 | 27502078 | ||||||
| chr16:27502093
|
C | CA | 22 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 28 | HG01106.hp2 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1908-750dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 11/36 | chr16 | 27502093 | ||||||
| chr16:27502314
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1907+545C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 11/36 | chr16 | 27502314 | ||||||
| chr16:27502538
|
A | G | 34 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(31): Show | 40 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1907+321T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 11/36 | chr16 | 27502538 | ||||||
| chr16:27503047
|
G | A | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1771-52C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503047 | ||||||
| chr16:27503179
|
A | T | 1 | a0001c0001t0001g0159 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1771-184T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503179 | ||||||
| chr16:27503180
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1771-185A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503180 | ||||||
| chr16:27503181
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1771-186G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503181 | ||||||
| chr16:27503339
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1771-344A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503339 | ||||||
| chr16:27503503
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1771-508G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503503 | ||||||
| chr16:27503510
|
C | T | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1771-515G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503510 | ||||||
| chr16:27503849
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1771-854C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503849 | ||||||
| chr16:27503857
|
C | A | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1771-862G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503857 | ||||||
| chr16:27503876
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1771-881A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503876 | ||||||
| chr16:27503994
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1771-999C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27503994 | ||||||
| chr16:27504031
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(63): Show | 82 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1771-1036G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504031 | ||||||
| chr16:27504039
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1771-1044A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504039 | ||||||
| chr16:27504304
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1771-1309C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504304 | ||||||
| chr16:27504314
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1771-1319C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504314 | ||||||
| chr16:27504370
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1771-1375G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504370 | ||||||
| chr16:27504430
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(34): Show | 48 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.1771-1435T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504430 | ||||||
| chr16:27504593
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0037others(1): Show | 5 | HG02970.hp2 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770+1306T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504593 | ||||||
| chr16:27504633
|
T | C | 1 | a0001c0001t0003g0006 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1770+1266A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504633 | ||||||
| chr16:27504641
|
C | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1770+1258G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504641 | ||||||
| chr16:27504676
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1770+1223C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504676 | ||||||
| chr16:27504784
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1770+1115T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504784 | ||||||
| chr16:27504925
|
T | C | 1 | a0001c0001t0001g0009 | 2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1770+974A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27504925 | ||||||
| chr16:27505012
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1770+887G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27505012 | ||||||
| chr16:27505013
|
G | A | 2 | a0001c0013t0001g0109a0009c0018t0001g0112 | 2 | HG02165.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1770+886C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27505013 | ||||||
| chr16:27505129
|
A | G | 1 | a0001c0008t0001g0014 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1770+770T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27505129 | ||||||
| chr16:27505184
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1770+715G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27505184 | ||||||
| chr16:27505319
|
G | C | 1 | a0002c0002t0001g0070 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1770+580C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27505319 | ||||||
| chr16:27505443
|
A | G | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1770+456T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27505443 | ||||||
| chr16:27505517
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1770+382A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27505517 | ||||||
| chr16:27505554
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA20805.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1770+345C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 10/36 | chr16 | 27505554 | ||||||
| chr16:27506350
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 15 | HG01109.hp1 HG02145.hp1 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.1553-234C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 9/36 | chr16 | 27506350 | ||||||
| chr16:27506504
|
T | A | 5 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(2): Show | 5 | HG01258.hp1 HG01361.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1552+343A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 9/36 | chr16 | 27506504 | ||||||
| chr16:27506505
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1552+342T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 9/36 | chr16 | 27506505 | ||||||
| chr16:27506601
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1552+246A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 9/36 | chr16 | 27506601 | ||||||
| chr16:27506633
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1552+214G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 9/36 | chr16 | 27506633 | ||||||
| chr16:27506690
|
CA | C | 1 | a0001c0001t0003g0002 | 4 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552+156delT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 9/36 | chr16 | 27506690 | ||||||
| chr16:27506714
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1552+133C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 9/36 | chr16 | 27506714 | ||||||
| chr16:27506757
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0101a0001c0001t0001g0111 | 3 | HG02129.hp1 NA18945.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1552+90G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 9/36 | chr16 | 27506757 | ||||||
| chr16:27507174
|
T | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1243-18A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507174 | ||||||
| chr16:27507327
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 15 | HG01109.hp1 HG02145.hp1 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.1243-171C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507327 | ||||||
| chr16:27507330
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1243-174T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507330 | ||||||
| chr16:27507399
|
A | AGGCTATG others(16): Show |
1 | a0001c0003t0001g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1243-266_1243-244d others(25): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507399 | ||||||
| chr16:27507538
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243-382G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507538 | ||||||
| chr16:27507574
|
C | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(33): Show | 47 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.1243-418G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507574 | ||||||
| chr16:27507707
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1243-551C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507707 | ||||||
| chr16:27507827
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1243-671A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507827 | ||||||
| chr16:27507840
|
C | T | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1243-684G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507840 | ||||||
| chr16:27507933
|
C | G | 2 | a0001c0001t0001g0041a0001c0022t0004g0021 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1242+607G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27507933 | ||||||
| chr16:27508079
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0037others(1): Show | 5 | HG02970.hp2 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+461C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27508079 | ||||||
| chr16:27508088
|
C | A | 1 | a0001c0003t0001g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1242+452G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 8/36 | chr16 | 27508088 | ||||||
| chr16:27509025
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1127-370A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509025 | ||||||
| chr16:27509153
|
A | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 29 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1127-498T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509153 | ||||||
| chr16:27509222
|
C | T | 1 | a0001c0003t0001g0028 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1127-567G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509222 | ||||||
| chr16:27509309
|
G | A | 1 | a0001c0007t0001g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1127-654C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509309 | ||||||
| chr16:27509338
|
A | G | 1 | a0001c0009t0001g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1127-683T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509338 | ||||||
| chr16:27509383
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0160 | 3 | HG02055.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1127-728C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509383 | ||||||
| chr16:27509471
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0096 | 2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1127-816G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509471 | ||||||
| chr16:27509472
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1127-817A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509472 | ||||||
| chr16:27509479
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1127-824G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509479 | ||||||
| chr16:27509532
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1127-877G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509532 | ||||||
| chr16:27509706
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1127-1051G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509706 | ||||||
| chr16:27509757
|
C | CA | 10 | a0001c0001t0001g0044a0001c0001t0001g0064a0001c0001t0001g0067others(7): Show | 10 | HG00423.hp1 HG00423.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1127-1103dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509757 | ||||||
| chr16:27509757
|
CA | C | 35 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(32): Show | 42 | HG01106.hp2 HG01109.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.1127-1103delT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509757 | ||||||
| chr16:27509757
|
CAAAAAAA others(2): Show |
C | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1127-1111_1127-110 others(13): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509757 | ||||||
| chr16:27509761
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1127-1106T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509761 | ||||||
| chr16:27509951
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1127-1296A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27509951 | ||||||
| chr16:27510047
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1127-1392C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27510047 | ||||||
| chr16:27510094
|
T | C | 13 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1127-1439A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27510094 | ||||||
| chr16:27510364
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1126+1385G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27510364 | ||||||
| chr16:27510424
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1126+1325C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27510424 | ||||||
| chr16:27510794
|
C | G | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 28 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126+955G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27510794 | ||||||
| chr16:27510841
|
A | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1126+908T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27510841 | ||||||
| chr16:27510906
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1126+843G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27510906 | ||||||
| chr16:27511057
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1126+692C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27511057 | ||||||
| chr16:27511286
|
G | A | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1126+463C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27511286 | ||||||
| chr16:27511344
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1126+405G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27511344 | ||||||
| chr16:27511390
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1126+359C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27511390 | ||||||
| chr16:27511554
|
A | G | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1126+195T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27511554 | ||||||
| chr16:27511638
|
C | T | 2 | a0001c0007t0001g0039a0001c0022t0004g0021 | 2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1126+111G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27511638 | ||||||
| chr16:27511674
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1126+75G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 7/36 | chr16 | 27511674 | ||||||
| chr16:27511931
|
A | C | 1 | a0001c0001t0001g0015 | 2 | NA18999.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.974-30T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27511931 | ||||||
| chr16:27511945
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.974-44A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27511945 | ||||||
| chr16:27511987
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(34): Show | 48 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.974-86T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27511987 | ||||||
| chr16:27512230
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.974-329G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27512230 | ||||||
| chr16:27512291
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG01109.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.974-390G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27512291 | ||||||
| chr16:27512292
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.974-391C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27512292 | ||||||
| chr16:27512319
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.974-418C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27512319 | ||||||
| chr16:27512375
|
A | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0114a0001c0001t0001g0140others(7): Show | 11 | HG01081.hp1 HG01258.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.974-474T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27512375 | ||||||
| chr16:27513016
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.974-1115A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27513016 | ||||||
| chr16:27513112
|
T | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.974-1211A>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27513112 | ||||||
| chr16:27513264
|
G | C | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.974-1363C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27513264 | ||||||
| chr16:27513408
|
C | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0114a0001c0001t0001g0140others(7): Show | 11 | HG01081.hp1 HG01258.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.974-1507G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27513408 | ||||||
| chr16:27513801
|
C | T | 1 | a0001c0001t0001g0017 | 2 | HG01515.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.974-1900G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27513801 | ||||||
| chr16:27513826
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.974-1925C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27513826 | ||||||
| chr16:27513955
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.974-2054G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27513955 | ||||||
| chr16:27514135
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.974-2234G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27514135 | ||||||
| chr16:27514260
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.974-2359C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27514260 | ||||||
| chr16:27514266
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.974-2365C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27514266 | ||||||
| chr16:27514326
|
C | T | 1 | a0002c0002t0006g0081 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.974-2425G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27514326 | ||||||
| chr16:27514455
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.974-2554G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27514455 | ||||||
| chr16:27515280
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.974-3379T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515280 | ||||||
| chr16:27515283
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.974-3382T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515283 | ||||||
| chr16:27515451
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.974-3550T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515451 | ||||||
| chr16:27515465
|
C | CA | 6 | a0001c0001t0001g0052a0001c0001t0001g0089a0001c0001t0001g0106others(3): Show | 6 | HG01358.hp1 HG02683.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.974-3565dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515465 | ||||||
| chr16:27515466
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.974-3565T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515466 | ||||||
| chr16:27515478
|
C | A | 1 | a0001c0001t0001g0054 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.974-3577G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515478 | ||||||
| chr16:27515728
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.974-3827C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515728 | ||||||
| chr16:27515780
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.974-3879T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515780 | ||||||
| chr16:27515879
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.974-3978G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515879 | ||||||
| chr16:27515911
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.974-4010T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27515911 | ||||||
| chr16:27516139
|
C | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0189 | 3 | HG01081.hp2 HG01099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.974-4238G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27516139 | ||||||
| chr16:27516491
|
A | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(153): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.974-4590T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27516491 | ||||||
| chr16:27516568
|
T | C | 1 | a0001c0001t0003g0006 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.974-4667A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27516568 | ||||||
| chr16:27517138
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.974-5237C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27517138 | ||||||
| chr16:27517798
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.974-5897G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27517798 | ||||||
| chr16:27517857
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.974-5956A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27517857 | ||||||
| chr16:27517859
|
A | T | 34 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(31): Show | 40 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.974-5958T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27517859 | ||||||
| chr16:27517922
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0107 | 3 | NA18941.hp2 NA18999.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.974-6021C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27517922 | ||||||
| chr16:27518188
|
G | GAC | 5 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0180others(2): Show | 5 | HG02155.hp1 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.974-6289_974-6288d others(4): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27518188 | ||||||
| chr16:27518188
|
G | GACAC | 5 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 6 | HG02970.hp2 HG03098.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-6291_974-6288d others(6): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27518188 | ||||||
| chr16:27518443
|
T | C | 1 | a0001c0003t0001g0005 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.974-6542A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27518443 | ||||||
| chr16:27519154
|
TG | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0114a0001c0001t0001g0140others(7): Show | 11 | HG01081.hp1 HG01258.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.974-7254delC | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27519154 | ||||||
| chr16:27519405
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.974-7504C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27519405 | ||||||
| chr16:27519483
|
C | T | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.974-7582G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27519483 | ||||||
| chr16:27519605
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.974-7704G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27519605 | ||||||
| chr16:27519905
|
G | A | 1 | a0002c0002t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.974-8004C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27519905 | ||||||
| chr16:27519960
|
A | T | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.974-8059T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27519960 | ||||||
| chr16:27520346
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.973+8252G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520346 | ||||||
| chr16:27520459
|
C | G | 1 | a0010c0017t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.973+8139G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520459 | ||||||
| chr16:27520459
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.973+8139G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520459 | ||||||
| chr16:27520464
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.973+8134G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520464 | ||||||
| chr16:27520656
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.973+7942G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520656 | ||||||
| chr16:27520726
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.973+7872A>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520726 | ||||||
| chr16:27520782
|
T | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(31): Show | 40 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.973+7816A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520782 | ||||||
| chr16:27520815
|
T | A | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.973+7783A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520815 | ||||||
| chr16:27520821
|
C | T | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.973+7777G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520821 | ||||||
| chr16:27520946
|
T | C | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(20): Show | 27 | HG00408.hp1 HG02074.hp1 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.973+7652A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27520946 | ||||||
| chr16:27521013
|
C | T | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.973+7585G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521013 | ||||||
| chr16:27521014
|
C | T | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.973+7584G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521014 | ||||||
| chr16:27521017
|
C | G | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.973+7581G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521017 | ||||||
| chr16:27521019
|
TCCCCAAT others(22): Show |
T | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.973+7550_973+7578d others(31): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521019 | ||||||
| chr16:27521049
|
A | G | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.973+7549T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521049 | ||||||
| chr16:27521171
|
C | G | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.973+7427G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521171 | ||||||
| chr16:27521373
|
C | T | 5 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(2): Show | 5 | HG01258.hp1 HG01361.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+7225G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521373 | ||||||
| chr16:27521534
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.973+7064C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521534 | ||||||
| chr16:27521892
|
A | T | 1 | a0001c0001t0001g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.973+6706T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521892 | ||||||
| chr16:27521993
|
T | C | 1 | a0001c0003t0001g0028 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.973+6605A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27521993 | ||||||
| chr16:27522085
|
A | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0061 | 3 | NA18967.hp2 NA18993.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.973+6513T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27522085 | ||||||
| chr16:27522473
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.973+6125C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27522473 | ||||||
| chr16:27522568
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.973+6030A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27522568 | ||||||
| chr16:27522579
|
C | A | 1 | a0001c0001t0001g0038 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.973+6019G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27522579 | ||||||
| chr16:27522647
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(34): Show | 48 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.973+5951T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27522647 | ||||||
| chr16:27522893
|
A | G | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+5705T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27522893 | ||||||
| chr16:27523135
|
C | T | 2 | a0004c0005t0001g0008a0004c0005t0001g0047 | 3 | HG02647.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.973+5463G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27523135 | ||||||
| chr16:27523582
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG01109.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.973+5016T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27523582 | ||||||
| chr16:27523633
|
A | G | 32 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(29): Show | 38 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.973+4965T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27523633 | ||||||
| chr16:27524223
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0002g0189a0001c0001t0002g0190others(1): Show | 5 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+4375C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27524223 | ||||||
| chr16:27524321
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.973+4277G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27524321 | ||||||
| chr16:27524400
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.973+4198C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27524400 | ||||||
| chr16:27524910
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.973+3688A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27524910 | ||||||
| chr16:27524984
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.973+3614A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27524984 | ||||||
| chr16:27525185
|
T | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066others(2): Show | 10 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+3413A>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525185 | ||||||
| chr16:27525185
|
T | TAAAAGAA others(3): Show |
16 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040others(13): Show | 16 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.973+3403_973+3412d others(12): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525185 | ||||||
| chr16:27525185
|
T | TAAAAGAA others(8): Show |
2 | a0001c0001t0001g0041a0002c0002t0001g0075 | 2 | HG01261.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.973+3398_973+3412d others(17): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525185 | ||||||
| chr16:27525185
|
T | TAAAAGAA others(13): Show |
11 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 13 | HG02258.hp2 HG02896.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.973+3393_973+3412d others(22): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525185 | ||||||
| chr16:27525185
|
T | TAAAAGAA others(18): Show |
1 | a0001c0001t0001g0034 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.973+3412_973+3413i others(27): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525185 | ||||||
| chr16:27525185
|
T | TAAAAGAA others(23): Show |
2 | a0001c0001t0003g0002a0001c0001t0003g0031 | 5 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+3412_973+3413i others(32): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525185 | ||||||
| chr16:27525185
|
T | TAAAAGAA others(33): Show |
1 | a0001c0001t0003g0006 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.973+3412_973+3413i others(42): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525185 | ||||||
| chr16:27525202
|
A | AAAGAAAA others(38): Show |
1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.973+3395_973+3396i others(47): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525202 | ||||||
| chr16:27525261
|
G | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(40): Show | 55 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.973+3337C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525261 | ||||||
| chr16:27525342
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.973+3256A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525342 | ||||||
| chr16:27525875
|
A | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(92): Show | 112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.973+2723T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525875 | ||||||
| chr16:27525938
|
G | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.973+2660C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525938 | ||||||
| chr16:27525951
|
G | GTT | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(189): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.973+2645_973+2646d others(4): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27525951 | ||||||
| chr16:27526191
|
G | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0091others(8): Show | 11 | HG00408.hp2 HG00423.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.973+2407C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27526191 | ||||||
| chr16:27526241
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.973+2357C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27526241 | ||||||
| chr16:27526287
|
TA | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0160 | 3 | HG02055.hp1 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.973+2310delT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27526287 | ||||||
| chr16:27526476
|
A | G | 1 | a0012c0015t0001g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.973+2122T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27526476 | ||||||
| chr16:27526519
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.973+2079C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27526519 | ||||||
| chr16:27526657
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.973+1941C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27526657 | ||||||
| chr16:27526774
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.973+1824T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27526774 | ||||||
| chr16:27526897
|
G | T | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.973+1701C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27526897 | ||||||
| chr16:27527195
|
G | A | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+1403C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27527195 | ||||||
| chr16:27527472
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.973+1126G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27527472 | ||||||
| chr16:27527592
|
A | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 16 | HG01109.hp1 HG02145.hp1 HG02896.hp2 others(13): Show |
intron_variant | MODIFIER | c.973+1006T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27527592 | ||||||
| chr16:27527764
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.973+834C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27527764 | ||||||
| chr16:27527921
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.973+677G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27527921 | ||||||
| chr16:27527958
|
A | G | 5 | a0001c0001t0001g0121a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 5 | HG01071.hp2 HG02300.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+640T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27527958 | ||||||
| chr16:27527973
|
CA | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(65): Show | 84 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.973+624delT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27527973 | ||||||
| chr16:27528012
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG02129.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.973+586C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27528012 | ||||||
| chr16:27528200
|
G | A | 32 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(29): Show | 38 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.973+398C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27528200 | ||||||
| chr16:27528230
|
G | A | 33 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(30): Show | 39 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.973+368C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 6/36 | chr16 | 27528230 | ||||||
| chr16:27528906
|
G | A | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.850-185C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27528906 | ||||||
| chr16:27529134
|
G | T | 1 | a0001c0001t0001g0017 | 2 | HG01515.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.850-413C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27529134 | ||||||
| chr16:27529214
|
C | T | 16 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(13): Show | 16 | HG00741.hp1 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.850-493G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27529214 | ||||||
| chr16:27529412
|
G | T | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.850-691C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27529412 | ||||||
| chr16:27529440
|
C | CA | 26 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(23): Show | 37 | HG01106.hp2 HG01109.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.850-720dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27529440 | ||||||
| chr16:27529440
|
C | CAA | 14 | a0001c0001t0003g0006a0001c0001t0003g0031a0002c0002t0001g0068others(11): Show | 15 | HG00099.hp2 HG00140.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.850-721_850-720dup others(2): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27529440 | ||||||
| chr16:27529981
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.850-1260C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27529981 | ||||||
| chr16:27530038
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-1317A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27530038 | ||||||
| chr16:27530119
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.850-1398A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27530119 | ||||||
| chr16:27530123
|
G | C | 1 | a0009c0018t0001g0112 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.850-1402C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27530123 | ||||||
| chr16:27530768
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.850-2047G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27530768 | ||||||
| chr16:27530795
|
C | T | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(20): Show | 27 | HG00408.hp1 HG02074.hp1 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.850-2074G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27530795 | ||||||
| chr16:27530824
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066others(1): Show | 9 | HG00140.hp2 HG02055.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-2103C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27530824 | ||||||
| chr16:27531126
|
C | T | 1 | a0010c0017t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.849+2165G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27531126 | ||||||
| chr16:27531516
|
G | A | 1 | a0001c0001t0003g0002 | 4 | HG01109.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+1775C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27531516 | ||||||
| chr16:27531602
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.849+1689G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27531602 | ||||||
| chr16:27531631
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849+1660A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27531631 | ||||||
| chr16:27531754
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.849+1537C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27531754 | ||||||
| chr16:27531815
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849+1476C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27531815 | ||||||
| chr16:27532039
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.849+1252C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27532039 | ||||||
| chr16:27532159
|
A | G | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849+1132T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27532159 | ||||||
| chr16:27532316
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.849+975G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27532316 | ||||||
| chr16:27532387
|
A | G | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849+904T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27532387 | ||||||
| chr16:27532457
|
C | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849+834G>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27532457 | ||||||
| chr16:27532482
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849+809G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27532482 | ||||||
| chr16:27532598
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.849+693G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27532598 | ||||||
| chr16:27532787
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849+504C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 5/36 | chr16 | 27532787 | ||||||
| chr16:27533579
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.753-192C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27533579 | ||||||
| chr16:27533718
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.753-331A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27533718 | ||||||
| chr16:27533938
|
G | A | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.753-551C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27533938 | ||||||
| chr16:27533961
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG02129.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.753-574C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27533961 | ||||||
| chr16:27534288
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.753-901A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27534288 | ||||||
| chr16:27534337
|
G | C | 1 | a0001c0001t0002g0190 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.753-950C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27534337 | ||||||
| chr16:27534676
|
G | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.753-1289C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27534676 | ||||||
| chr16:27534881
|
G | T | 17 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(14): Show | 17 | HG00741.hp1 HG01099.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.753-1494C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27534881 | ||||||
| chr16:27534969
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.753-1582T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27534969 | ||||||
| chr16:27535219
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.753-1832G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27535219 | ||||||
| chr16:27535330
|
T | A | 3 | a0001c0001t0001g0154a0001c0009t0001g0155a0001c0009t0001g0185 | 3 | HG03225.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.753-1943A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27535330 | ||||||
| chr16:27535488
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.753-2101A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27535488 | ||||||
| chr16:27535574
|
T | TA | 26 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 31 | HG00408.hp1 HG01243.hp2 HG02074.hp1 others(28): Show |
intron_variant | MODIFIER | c.753-2188dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27535574 | ||||||
| chr16:27535655
|
G | A | 1 | a0001c0001t0001g0012 | 2 | NA18962.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.752+2129C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27535655 | ||||||
| chr16:27535954
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.752+1830A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27535954 | ||||||
| chr16:27536331
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.752+1453C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27536331 | ||||||
| chr16:27536335
|
G | A | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.752+1449C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27536335 | ||||||
| chr16:27536443
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.752+1341C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27536443 | ||||||
| chr16:27536564
|
A | G | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.752+1220T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27536564 | ||||||
| chr16:27536727
|
TCCA | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0157a0001c0001t0001g0168 | 4 | HG02109.hp2 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.752+1054_752+1056d others(5): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27536727 | ||||||
| chr16:27536785
|
C | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(121): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.752+999G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27536785 | ||||||
| chr16:27536803
|
G | A | 1 | a0001c0019t0001g0085 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.752+981C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27536803 | ||||||
| chr16:27536973
|
C | G | 1 | a0001c0001t0001g0167 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.752+811G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27536973 | ||||||
| chr16:27537355
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.752+429T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27537355 | ||||||
| chr16:27537388
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0107 | 3 | NA18941.hp2 NA18999.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.752+396A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27537388 | ||||||
| chr16:27537696
|
C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 16 | HG01109.hp1 HG02145.hp1 HG02896.hp2 others(13): Show |
intron_variant | MODIFIER | c.752+88G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 4/36 | chr16 | 27537696 | ||||||
| chr16:27538103
|
A | G | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.608+77T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 3/36 | chr16 | 27538103 | ||||||
| chr16:27538597
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.432-241T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27538597 | ||||||
| chr16:27538786
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.432-430C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27538786 | ||||||
| chr16:27538971
|
T | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0049a0001c0001t0001g0111others(4): Show | 7 | HG01071.hp1 HG02129.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.432-615A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27538971 | ||||||
| chr16:27538971
|
T | TAC | 25 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(22): Show | 28 | HG00408.hp1 HG01081.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.432-617_432-616dup others(2): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27538971 | ||||||
| chr16:27538971
|
TAC | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(10): Show | 23 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.432-617_432-616del others(2): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27538971 | ||||||
| chr16:27538971
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0119 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.432-625_432-616del others(10): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27538971 | ||||||
| chr16:27538971
|
TACACACA others(5): Show |
T | 2 | a0004c0005t0001g0008a0004c0005t0001g0047 | 3 | HG02647.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.432-627_432-616del others(12): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27538971 | ||||||
| chr16:27539004
|
C | CT | 25 | a0001c0001t0001g0050a0001c0001t0001g0083a0001c0001t0001g0089others(22): Show | 27 | HG00408.hp2 HG00423.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.432-649dupA | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27539004 | ||||||
| chr16:27539004
|
CT | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 6 | HG02165.hp2 HG03041.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-649delA | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27539004 | ||||||
| chr16:27539114
|
G | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.432-758C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27539114 | ||||||
| chr16:27539129
|
T | C | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.432-773A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27539129 | ||||||
| chr16:27539133
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(156): Show | 180 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.432-777T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27539133 | ||||||
| chr16:27539280
|
A | G | 1 | a0013c0020t0001g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.432-924T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27539280 | ||||||
| chr16:27539317
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.432-961T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27539317 | ||||||
| chr16:27539795
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(156): Show | 180 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.432-1439T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27539795 | ||||||
| chr16:27539885
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.432-1529A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27539885 | ||||||
| chr16:27540016
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(186): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.432-1660G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27540016 | ||||||
| chr16:27540085
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.432-1729G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27540085 | ||||||
| chr16:27540229
|
A | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.432-1873T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27540229 | ||||||
| chr16:27540274
|
A | G | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.432-1918T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27540274 | ||||||
| chr16:27540305
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.432-1949T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27540305 | ||||||
| chr16:27540458
|
C | G | 1 | a0008c0012t0001g0030 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.432-2102G>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27540458 | ||||||
| chr16:27540520
|
G | T | 6 | a0001c0001t0001g0067a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 7 | HG00423.hp2 HG03834.hp2 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.432-2164C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27540520 | ||||||
| chr16:27540904
|
G | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 28 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.432-2548C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27540904 | ||||||
| chr16:27540921
|
A | T | 3 | a0001c0007t0001g0029a0001c0007t0001g0039a0001c0007t0001g0040 | 3 | HG01243.hp1 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.432-2565T>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27540921 | ||||||
| chr16:27541206
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.432-2850C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27541206 | ||||||
| chr16:27541266
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.432-2910G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27541266 | ||||||
| chr16:27541414
|
T | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(154): Show | 178 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.432-3058A>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27541414 | ||||||
| chr16:27541700
|
G | A | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.432-3344C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27541700 | ||||||
| chr16:27541774
|
C | T | 8 | a0001c0001t0002g0004a0001c0001t0002g0020a0001c0001t0002g0171others(5): Show | 11 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.432-3418G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27541774 | ||||||
| chr16:27541943
|
G | A | 2 | a0005c0010t0001g0170a0005c0010t0001g0183 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.431+3371C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27541943 | ||||||
| chr16:27542193
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.431+3121G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27542193 | ||||||
| chr16:27542431
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.431+2883C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27542431 | ||||||
| chr16:27542567
|
G | GA | 29 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(26): Show | 37 | HG00099.hp1 HG00639.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.431+2746dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27542567 | ||||||
| chr16:27543339
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.431+1975G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27543339 | ||||||
| chr16:27543427
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.431+1887T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27543427 | ||||||
| chr16:27543505
|
C | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(121): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.431+1809G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27543505 | ||||||
| chr16:27543626
|
A | G | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.431+1688T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27543626 | ||||||
| chr16:27543635
|
T | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(153): Show | 172 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.431+1679A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27543635 | ||||||
| chr16:27543689
|
C | T | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.431+1625G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27543689 | ||||||
| chr16:27543757
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.431+1557A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27543757 | ||||||
| chr16:27543941
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.431+1373C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27543941 | ||||||
| chr16:27544286
|
A | G | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.431+1028T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544286 | ||||||
| chr16:27544348
|
G | A | 1 | a0009c0018t0001g0112 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.431+966C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544348 | ||||||
| chr16:27544367
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.431+947T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544367 | ||||||
| chr16:27544399
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0065 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.431+915C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544399 | ||||||
| chr16:27544458
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431+856G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544458 | ||||||
| chr16:27544538
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.431+776G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544538 | ||||||
| chr16:27544628
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.431+686C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544628 | ||||||
| chr16:27544826
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.431+488G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544826 | ||||||
| chr16:27544934
|
C | T | 38 | a0001c0001t0001g0015a0001c0001t0001g0083a0001c0001t0001g0084others(35): Show | 40 | HG00408.hp2 HG00423.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.431+380G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544934 | ||||||
| chr16:27544961
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.431+353T>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544961 | ||||||
| chr16:27544974
|
CT | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(158): Show | 182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.431+339delA | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27544974 | ||||||
| chr16:27545029
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.431+285C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27545029 | ||||||
| chr16:27545097
|
C | T | 2 | a0001c0001t0001g0084a0001c0019t0001g0085 | 2 | NA18995.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.431+217G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 2/36 | chr16 | 27545097 | ||||||
| chr16:27545552
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.222-29G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27545552 | ||||||
| chr16:27545748
|
T | G | 1 | a0005c0010t0001g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.222-225A>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27545748 | ||||||
| chr16:27546010
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.222-487C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546010 | ||||||
| chr16:27546428
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(121): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.222-905A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546428 | ||||||
| chr16:27546472
|
GT | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 7 | HG02970.hp2 HG03098.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-950delA | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546472 | ||||||
| chr16:27546485
|
T | G | 6 | a0001c0001t0001g0184a0001c0001t0002g0020a0001c0001t0002g0189others(3): Show | 7 | HG00639.hp2 HG01081.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-962A>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546485 | ||||||
| chr16:27546485
|
T | TTG | 3 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0005g0066 | 8 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-963_222-962ins others(2): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546485 | ||||||
| chr16:27546486
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0184others(6): Show | 15 | HG00639.hp2 HG01081.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.222-963C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546486 | ||||||
| chr16:27546486
|
G | GA | 78 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(75): Show | 86 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.222-964dupT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546486 | ||||||
| chr16:27546486
|
G | T | 1 | a0001c0001t0001g0043 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.222-963C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546486 | ||||||
| chr16:27546486
|
GA | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0083others(4): Show | 8 | HG00099.hp2 HG00140.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.222-964delT | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546486 | ||||||
| chr16:27546486
|
GAA | G | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-965_222-964del others(2): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546486 | ||||||
| chr16:27546487
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.222-964T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546487 | ||||||
| chr16:27546507
|
C | CAT | 2 | a0001c0001t0001g0042a0001c0022t0004g0021 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.222-986_222-985dup others(2): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546507 | ||||||
| chr16:27546513
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.222-990A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546513 | ||||||
| chr16:27546835
|
C | T | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-1312G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546835 | ||||||
| chr16:27546852
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(157): Show | 181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.222-1329A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27546852 | ||||||
| chr16:27547051
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(155): Show | 179 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.222-1528C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27547051 | ||||||
| chr16:27547238
|
G | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(121): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.222-1715C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27547238 | ||||||
| chr16:27547350
|
A | G | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.222-1827T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27547350 | ||||||
| chr16:27547554
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.222-2031C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27547554 | ||||||
| chr16:27547562
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG00423.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.222-2039A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27547562 | ||||||
| chr16:27547781
|
C | T | 1 | a0001c0001t0003g0006 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.221+1889G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27547781 | ||||||
| chr16:27547851
|
C | T | 5 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(2): Show | 5 | HG01258.hp1 HG01361.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+1819G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27547851 | ||||||
| chr16:27547858
|
C | T | 5 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(2): Show | 5 | HG01258.hp1 HG01361.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+1812G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27547858 | ||||||
| chr16:27547953
|
G | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.221+1717C>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27547953 | ||||||
| chr16:27548456
|
A | G | 1 | a0001c0024t0001g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.221+1214T>C | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27548456 | ||||||
| chr16:27548494
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(176): Show | 206 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.221+1176G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27548494 | ||||||
| chr16:27548579
|
T | C | 4 | a0001c0001t0002g0020a0001c0001t0002g0189a0001c0001t0002g0190others(1): Show | 5 | HG00639.hp2 HG01081.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+1091A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27548579 | ||||||
| chr16:27548608
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.221+1062G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27548608 | ||||||
| chr16:27548822
|
T | C | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.221+848A>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27548822 | ||||||
| chr16:27548854
|
TTC | T | 4 | a0001c0003t0001g0005a0001c0003t0001g0026a0001c0003t0001g0027others(1): Show | 5 | HG02258.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+814_221+815del others(2): Show |
GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27548854 | ||||||
| chr16:27548986
|
C | T | 1 | a0001c0022t0004g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.221+684G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27548986 | ||||||
| chr16:27549011
|
G | A | 1 | a0002c0002t0006g0081 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.221+659C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27549011 | ||||||
| chr16:27549115
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.221+555C>G | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27549115 | ||||||
| chr16:27549444
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.221+226G>A | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27549444 | ||||||
| chr16:27549565
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(120): Show | 134 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.221+105C>T | GTF3C1 | ENSG00000077235.18 | transcript | ENST00000356183.9 | protein_coding | 1/36 | chr16 | 27549565 |