Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 53630 |
|---|---|
| ensemblid | ENSG00000135697.10 |
| hgncid | 13815 |
| symbol | BCO1 |
| name | beta-carotene oxygenase 1 |
| refseq_nuc | NM_017429.3 |
| refseq_prot | NP_059125.2 |
| ensembl_nuc | ENST00000258168.7 |
| ensembl_prot | ENSP00000258168.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 81238689 |
| end | 81291142 |
| strand | + |
| ver | v1.2 |
| region | chr16:81238689-81291142 |
| region5000 | chr16:81233689-81296142 |
| regionname0 | BCO1_chr16_81238689_81291142 |
| regionname5000 | BCO1_chr16_81233689_81296142 |
| 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 | 547 | 263 | 80 | 40 | 113 | 4 | 24 | 82 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0002 | 0/0 | 547 | 68 | 8 | 22 | 22 | 8 | 8 | 16 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0003 | 0/0 | 547 | 55 | 1 | 10 | 30 | 5 | 9 | 20 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0004 | 0/0 | 547 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0005 | 0/0 | 547 | 3 | 0 | 1 | 1 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0006 | 0/0 | 547 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0007 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0008 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0009 | 0/0 | 547 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0010 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0011 | 0/0 | 547 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0012 | 0/0 | 547 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0013 | 0/0 | 547 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0014 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| 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 | 1/0 | 1644 | 160 | 31 | 26 | 79 | 3 | 20 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0002 | 0/0 | 1644 | 56 | 15 | 4 | 34 | 0 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0003 | 0/0 | 1644 | 52 | 1 | 10 | 29 | 5 | 7 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0004 | 0/0 | 1644 | 45 | 3 | 14 | 20 | 5 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0005 | 0/0 | 1644 | 39 | 28 | 9 | 0 | 1 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0006 | 0/0 | 1644 | 21 | 4 | 8 | 2 | 3 | 4 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0007 | 0/0 | 1644 | 5 | 5 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0008 | 0/0 | 1644 | 3 | 0 | 3 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0009 | 0/0 | 1644 | 3 | 0 | 0 | 1 | 0 | 2 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0010 | 0/0 | 1644 | 2 | 0 | 0 | 1 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0011 | 0/1 | 1644 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0012 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0013 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0014 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0015 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0016 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0017 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0018 | 0/0 | 1644 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0019 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0020 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0021 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0022 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0023 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0024 | 0/0 | 1644 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0025 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| c0026 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| 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 | 786 | 392 | 94 | 68 | 166 | 18 | 44 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| t0002 | 0/0 | 786 | 10 | 0 | 8 | 2 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| 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 | 1/0 | 1644 | 160 | 31 | 26 | 79 | 3 | 20 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0002 | 0/0 | 1644 | 56 | 15 | 4 | 34 | 0 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0005 | 0/0 | 1644 | 39 | 28 | 9 | 0 | 1 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0007 | 0/0 | 1644 | 5 | 5 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0011 | 0/1 | 1644 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0017 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0018 | 0/0 | 1644 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0002c0004 | 0/0 | 1644 | 45 | 3 | 14 | 20 | 5 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0002c0006 | 0/0 | 1644 | 21 | 4 | 8 | 2 | 3 | 4 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0002c0020 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0002c0022 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0003c0003 | 0/0 | 1644 | 52 | 1 | 10 | 29 | 5 | 7 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0003c0009 | 0/0 | 1644 | 3 | 0 | 0 | 1 | 0 | 2 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0004c0008 | 0/0 | 1644 | 3 | 0 | 3 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0005c0010 | 0/0 | 1644 | 2 | 0 | 0 | 1 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0005c0024 | 0/0 | 1644 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0006c0014 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0006c0016 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0007c0026 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0008c0013 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0009c0021 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0010c0015 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0011c0023 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0012c0012 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0013c0019 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0014c0025 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2429 | 151 | 31 | 18 | 78 | 3 | 20 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0001t0002 | 0/0 | 2429 | 9 | 0 | 8 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0002t0001 | 0/0 | 2429 | 55 | 15 | 4 | 33 | 0 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0002t0002 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0005t0001 | 0/0 | 2429 | 39 | 28 | 9 | 0 | 1 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0007t0001 | 0/0 | 2429 | 5 | 5 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0011t0001 | 0/1 | 2429 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0017t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0001c0018t0001 | 0/0 | 2429 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0002c0004t0001 | 0/0 | 2429 | 45 | 3 | 14 | 20 | 5 | 3 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0002c0006t0001 | 0/0 | 2429 | 21 | 4 | 8 | 2 | 3 | 4 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0002c0020t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0002c0022t0001 | 0/0 | 2429 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0003c0003t0001 | 0/0 | 2429 | 52 | 1 | 10 | 29 | 5 | 7 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0003c0009t0001 | 0/0 | 2429 | 3 | 0 | 0 | 1 | 0 | 2 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0004c0008t0001 | 0/0 | 2429 | 3 | 0 | 3 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0005c0010t0001 | 0/0 | 2429 | 2 | 0 | 0 | 1 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0005c0024t0001 | 0/0 | 2429 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0006c0014t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0006c0016t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0007c0026t0001 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0008c0013t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0009c0021t0001 | 0/0 | 2429 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0010c0015t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0011c0023t0001 | 0/0 | 2429 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0012c0012t0001 | 0/0 | 2429 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0013c0019t0001 | 0/0 | 2429 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| a0014c0025t0001 | 0/0 | 2429 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | copy fasta | chr16 | 81233689 | 81296142 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0001g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0001t0002g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0005t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0007t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0011t0001g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0017t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0001c0018t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0006t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0020t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0002c0022t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0003t0001g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0009t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0003c0009t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0004c0008t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0004c0008t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0004c0008t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0005c0010t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0005c0010t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0005c0024t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0006c0014t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0006c0016t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0007c0026t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0008c0013t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0009c0021t0001g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0010c0015t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0011c0023t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0012c0012t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0013c0019t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| a0014c0025t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0001 | g0139 | EUR | GBR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00099 | hp2 | a0002 | c0006 | t0001 | g0312 | EUR | GBR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00140 | hp1 | a0002 | c0006 | t0001 | g0250 | EUR | GBR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0332 | EUR | GBR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00280 | hp2 | a0001 | c0005 | t0001 | g0020 | EUR | FIN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00323 | hp1 | a0002 | c0004 | t0001 | g0110 | EUR | FIN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00323 | hp2 | a0011 | c0023 | t0001 | g0174 | EUR | FIN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00558 | hp2 | a0002 | c0004 | t0001 | g0145 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00597 | hp1 | a0002 | c0004 | t0001 | g0130 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00609 | hp1 | a0002 | c0004 | t0001 | g0055 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00609 | hp2 | a0002 | c0006 | t0001 | g0378 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0328 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00639 | hp2 | a0001 | c0005 | t0001 | g0117 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0316 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00733 | hp1 | a0001 | c0005 | t0001 | g0026 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0354 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00735 | hp2 | a0001 | c0018 | t0001 | g0276 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00738 | hp1 | a0002 | c0004 | t0001 | g0109 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00738 | hp2 | a0004 | c0008 | t0001 | g0054 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00741 | hp1 | a0004 | c0008 | t0001 | g0084 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG00741 | hp2 | a0002 | c0004 | t0001 | g0108 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01074 | hp1 | a0002 | c0006 | t0001 | g0314 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01074 | hp2 | a0001 | c0005 | t0001 | g0021 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01081 | hp2 | a0002 | c0004 | t0001 | g0141 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01099 | hp1 | a0002 | c0004 | t0001 | g0092 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0390 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01106 | hp1 | a0005 | c0024 | t0001 | g0384 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01109 | hp1 | a0002 | c0004 | t0001 | g0080 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0105 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0309 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01167 | hp2 | a0002 | c0004 | t0001 | g0103 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01168 | hp1 | a0001 | c0005 | t0001 | g0022 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01169 | hp2 | a0002 | c0004 | t0001 | g0104 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0360 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01192 | hp1 | a0004 | c0008 | t0001 | g0096 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0379 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0121 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0387 | AMR | PUR | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01255 | hp1 | a0002 | c0006 | t0001 | g0311 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0376 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01256 | hp1 | a0002 | c0006 | t0001 | g0245 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01256 | hp2 | a0001 | c0005 | t0001 | g0023 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01257 | hp1 | a0002 | c0004 | t0001 | g0004 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0385 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01258 | hp1 | a0002 | c0004 | t0001 | g0004 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01258 | hp2 | a0001 | c0005 | t0001 | g0024 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01261 | hp1 | a0001 | c0005 | t0001 | g0025 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01346 | hp1 | a0002 | c0006 | t0001 | g0186 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0382 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01358 | hp1 | a0002 | c0004 | t0001 | g0140 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01358 | hp2 | a0002 | c0006 | t0001 | g0310 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01361 | hp1 | a0002 | c0006 | t0001 | g0389 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01361 | hp2 | a0002 | c0004 | t0001 | g0090 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0033 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01433 | hp2 | a0001 | c0005 | t0001 | g0136 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0386 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0293 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01515 | hp1 | a0002 | c0004 | t0001 | g0047 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0322 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0324 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0007 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01517 | hp1 | a0002 | c0004 | t0001 | g0048 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0007 | EUR | IBS | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0125 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0030 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0359 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0349 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0346 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0383 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01978 | hp2 | a0002 | c0004 | t0001 | g0142 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0372 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0368 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01993 | hp2 | a0002 | c0004 | t0001 | g0039 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02004 | hp2 | a0003 | c0003 | t0001 | g0303 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0336 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0320 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0335 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02055 | hp2 | a0002 | c0006 | t0001 | g0028 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0357 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0377 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02083 | hp2 | a0002 | c0004 | t0001 | g0053 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02129 | hp2 | a0005 | c0010 | t0001 | g0095 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0228 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0155 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02155 | hp1 | a0002 | c0004 | t0001 | g0082 | EAS | CDX | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0301 | EAS | CDX | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02257 | hp2 | a0002 | c0004 | t0001 | g0168 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02258 | hp2 | a0001 | c0005 | t0001 | g0120 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0027 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02293 | hp2 | a0002 | c0006 | t0001 | g0222 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02300 | hp1 | a0002 | c0006 | t0001 | g0150 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0375 | AMR | PEL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0031 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0202 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | KHV | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0323 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02602 | hp2 | a0001 | c0005 | t0001 | g0091 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0153 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0119 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02630 | hp1 | a0001 | c0007 | t0001 | g0392 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0313 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02698 | hp1 | a0005 | c0010 | t0001 | g0343 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0156 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02723 | hp2 | a0001 | c0005 | t0001 | g0112 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02738 | hp1 | a0002 | c0004 | t0001 | g0102 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0340 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0131 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0097 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02896 | hp1 | a0002 | c0004 | t0001 | g0009 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0122 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02897 | hp2 | a0002 | c0004 | t0001 | g0011 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02922 | hp1 | a0010 | c0015 | t0001 | g0154 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02965 | hp1 | a0008 | c0013 | t0001 | g0029 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02976 | hp2 | a0006 | c0014 | t0001 | g0098 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03041 | hp2 | a0002 | c0020 | t0001 | g0275 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0148 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03098 | hp2 | a0002 | c0006 | t0001 | g0163 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03139 | hp1 | a0001 | c0007 | t0001 | g0162 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0118 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0138 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0132 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0137 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0251 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03453 | hp1 | a0001 | c0007 | t0001 | g0235 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0358 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03490 | hp2 | a0013 | c0019 | t0001 | g0188 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03491 | hp1 | a0002 | c0004 | t0001 | g0134 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03491 | hp2 | a0003 | c0003 | t0001 | g0194 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0196 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03516 | hp1 | a0006 | c0016 | t0001 | g0010 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0115 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0113 | AFR | GWD | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0111 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03654 | hp2 | a0002 | c0006 | t0001 | g0249 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03688 | hp1 | a0002 | c0006 | t0001 | g0243 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03704 | hp1 | a0003 | c0003 | t0001 | g0239 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0366 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03831 | hp2 | a0003 | c0009 | t0001 | g0171 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03927 | hp2 | a0002 | c0006 | t0001 | g0248 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03942 | hp1 | a0002 | c0022 | t0001 | g0333 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04184 | hp1 | a0002 | c0004 | t0001 | g0079 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04184 | hp2 | a0009 | c0021 | t0001 | g0391 | SAS | BEB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG04228 | hp2 | a0003 | c0009 | t0001 | g0088 | SAS | STU | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18522 | hp1 | a0012 | c0012 | t0001 | g0152 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0114 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0334 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18940 | hp2 | a0003 | c0009 | t0001 | g0052 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18943 | hp1 | a0003 | c0003 | t0001 | g0339 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18945 | hp2 | a0002 | c0004 | t0001 | g0129 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0351 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0367 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18950 | hp2 | a0002 | c0004 | t0001 | g0093 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18952 | hp2 | a0002 | c0004 | t0001 | g0078 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18961 | hp1 | a0003 | c0003 | t0001 | g0177 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18961 | hp2 | a0014 | c0025 | t0001 | g0302 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0291 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0371 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18964 | hp2 | a0002 | c0004 | t0001 | g0032 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18968 | hp1 | a0002 | c0004 | t0001 | g0035 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0200 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18973 | hp1 | a0002 | c0004 | t0001 | g0050 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18975 | hp1 | a0002 | c0004 | t0001 | g0065 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18978 | hp2 | a0003 | c0003 | t0001 | g0369 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18982 | hp2 | a0002 | c0004 | t0001 | g0044 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18988 | hp1 | a0002 | c0004 | t0001 | g0099 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0338 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18990 | hp1 | a0002 | c0006 | t0001 | g0364 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0363 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18998 | hp2 | a0002 | c0004 | t0001 | g0106 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18999 | hp2 | a0002 | c0004 | t0001 | g0144 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0365 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0319 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19005 | hp1 | a0002 | c0004 | t0001 | g0066 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19009 | hp1 | a0003 | c0003 | t0001 | g0327 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0304 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0124 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19043 | hp1 | a0001 | c0007 | t0001 | g0201 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19043 | hp2 | a0001 | c0017 | t0001 | g0133 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19058 | hp2 | a0002 | c0004 | t0001 | g0051 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19062 | hp1 | a0002 | c0004 | t0001 | g0094 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0337 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19068 | hp1 | a0003 | c0003 | t0001 | g0388 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0064 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19078 | hp1 | a0003 | c0003 | t0001 | g0246 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19087 | hp1 | a0007 | c0026 | t0001 | g0370 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0012 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0126 | AFR | YRI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ASW | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ASW | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0326 | EUR | TSI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20752 | hp2 | a0002 | c0006 | t0001 | g0315 | EUR | TSI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0380 | EUR | TSI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20805 | hp2 | a0002 | c0004 | t0001 | g0128 | EUR | TSI | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0381 | SAS | GIH | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20905 | hp2 | a0002 | c0006 | t0001 | g0321 | SAS | GIH | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0356 | AMR | CLM | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0143 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0116 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0151 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | ACB | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03471 | hp1 | a0002 | c0006 | t0001 | g0173 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | USA | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0393 | AFR | USA | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20300 | hp1 | a0002 | c0006 | t0001 | g0238 | AFR | USA | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0373 | AFR | USA | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA21309 | hp1 | a0001 | c0005 | t0001 | g0167 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | LWK | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0011 | t0001 | g0081 | REF | REF | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0236 | REF | REF | BCO1_chr16_81233689_81296142 | BCO1 | chr16 | 81233689 | 81296142 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81259740
|
C | G | 1 | a0007 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.258C>G | p.Asn86Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/11 | 478/2429 | 258/1644 | 86/547 | chr16 | 81259740 | ||
| chr16:81262242
|
A | G | 1 | a0014 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.430A>G | p.Ile144Val | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/11 | 650/2429 | 430/1644 | 144/547 | chr16 | 81262242 | ||
| chr16:81264700
|
G | C | 1 | a0013 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.532G>C | p.Ala178Pro | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/11 | 752/2429 | 532/1644 | 178/547 | chr16 | 81264700 | ||
| chr16:81264736
|
G | A | 1 | a0012 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.568G>A | p.Glu190Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/11 | 788/2429 | 568/1644 | 190/547 | chr16 | 81264736 | ||
| chr16:81268089
|
A | T | 3 | a0002a0005a0011 | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
missense_variant | MODERATE | c.801A>T | p.Arg267Ser | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/11 | 1021/2429 | 801/1644 | 267/547 | chr16 | 81268089 | ||
| chr16:81270294
|
G | A | 1 | a0010 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.979G>A | p.Glu327Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/11 | 1199/2429 | 979/1644 | 327/547 | chr16 | 81270294 | ||
| chr16:81280891
|
C | T | 4 | a0003a0005a0007others(1): Show | 60 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
missense_variant | MODERATE | c.1136C>T | p.Ala379Val | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/11 | 1356/2429 | 1136/1644 | 379/547 | chr16 | 81280891 | ||
| chr16:81285618
|
G | C | 1 | a0009 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1286G>C | p.Ser429Thr | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/11 | 1506/2429 | 1286/1644 | 429/547 | chr16 | 81285618 | ||
| chr16:81290521
|
G | A | 1 | a0008 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.1588G>A | p.Ala530Thr | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 11/11 | 1808/2429 | 1588/1644 | 530/547 | chr16 | 81290521 | ||
| chr16:81290543
|
G | A | 1 | a0006 | 2 | HG02976.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.1610G>A | p.Arg537Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 11/11 | 1830/2429 | 1610/1644 | 537/547 | chr16 | 81290543 | ||
| chr16:81290555
|
G | A | 2 | a0004a0011 | 4 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(1): Show |
missense_variant | MODERATE | c.1622G>A | p.Cys541Tyr | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 11/11 | 1842/2429 | 1622/1644 | 541/547 | chr16 | 81290555 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81245515
|
T | C | 13 | a0001c0002a0001c0005a0001c0011others(10): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
synonymous_variant | LOW | c.105T>C | p.Asn35Asn | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/11 | 325/2429 | 105/1644 | 35/547 | chr16 | 81245515 | ||
| chr16:81262175
|
C | A | 2 | a0001c0011a0001c0018 | 2 | HG00735.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.363C>A | p.Thr121Thr | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/11 | 583/2429 | 363/1644 | 121/547 | chr16 | 81262175 | ||
| chr16:81264747
|
G | A | 1 | a0002c0020 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.579G>A | p.Lys193Lys | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/11 | 799/2429 | 579/1644 | 193/547 | chr16 | 81264747 | ||
| chr16:81267966
|
A | G | 5 | a0001c0005a0001c0007a0001c0017others(2): Show | 47 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(44): Show |
synonymous_variant | LOW | c.678A>G | p.Pro226Pro | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/11 | 898/2429 | 678/1644 | 226/547 | chr16 | 81267966 | ||
| chr16:81270320
|
C | T | 1 | a0001c0017 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1005C>T | p.Phe335Phe | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/11 | 1225/2429 | 1005/1644 | 335/547 | chr16 | 81270320 | ||
| chr16:81285598
|
T | C | 1 | a0002c0022 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1266T>C | p.Phe422Phe | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/11 | 1486/2429 | 1266/1644 | 422/547 | chr16 | 81285598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81290719
|
C | A | 2 | a0001c0001t0002a0001c0002t0002 | 10 | HG01099.hp2 HG01255.hp2 HG01928.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*142C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 11/11 | 142 | chr16 | 81290719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81238991
|
A | G | 1 | a0001c0001t0001g0393 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64+19A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81238991 | ||||||
| chr16:81239020
|
A | AT | 30 | a0001c0001t0001g0361a0001c0001t0001g0362a0001c0001t0001g0366others(27): Show | 30 | HG00609.hp2 HG00621.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.64+62dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81239020 | |||||
| chr16:81239020
|
A | T | 2 | a0001c0007t0001g0392a0009c0021t0001g0391 | 2 | HG02630.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.64+48A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239020 | ||||||
| chr16:81239020
|
AT | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(125): Show | 131 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.64+62delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81239020 | |||||
| chr16:81239020
|
ATT | A | 15 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(12): Show | 15 | HG00735.hp1 HG01070.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+61_64+62delTT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81239020 | |||||
| chr16:81239023
|
T | A | 8 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(5): Show | 8 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+51T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239023 | ||||||
| chr16:81239025
|
T | A | 11 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(8): Show | 11 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+53T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239025 | ||||||
| chr16:81239164
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.64+192C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239164 | ||||||
| chr16:81239178
|
G | A | 8 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(5): Show | 8 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+206G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239178 | ||||||
| chr16:81239220
|
T | C | 1 | a0003c0003t0001g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64+248T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239220 | ||||||
| chr16:81239276
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.64+304G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239276 | ||||||
| chr16:81239314
|
G | T | 4 | a0001c0005t0001g0153a0001c0005t0001g0155a0001c0005t0001g0156others(1): Show | 4 | HG02145.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+342G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239314 | ||||||
| chr16:81239444
|
T | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(2): Show | 5 | HG02647.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+472T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239444 | ||||||
| chr16:81239465
|
G | A | 3 | a0001c0002t0002g0034a0002c0004t0001g0032a0002c0004t0001g0033 | 3 | HG01433.hp1 HG02071.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.64+493G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239465 | ||||||
| chr16:81239546
|
A | G | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64+574A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239546 | ||||||
| chr16:81239652
|
C | T | 1 | a0001c0005t0001g0156 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.64+680C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239652 | ||||||
| chr16:81239653
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.64+681G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239653 | ||||||
| chr16:81239903
|
G | T | 2 | a0001c0005t0001g0030a0001c0005t0001g0031 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.64+931G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81239903 | ||||||
| chr16:81240264
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(126): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.64+1292T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240264 | ||||||
| chr16:81240373
|
C | G | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.64+1401C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240373 | ||||||
| chr16:81240396
|
T | C | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1424T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240396 | ||||||
| chr16:81240410
|
A | C | 5 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(2): Show | 5 | HG02647.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1438A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240410 | ||||||
| chr16:81240419
|
C | T | 1 | a0003c0003t0001g0360 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.64+1447C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240419 | ||||||
| chr16:81240462
|
T | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1490T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240462 | ||||||
| chr16:81240464
|
C | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(152): Show | 158 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.64+1492C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240464 | ||||||
| chr16:81240594
|
A | G | 1 | a0001c0002t0001g0146 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.64+1622A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240594 | ||||||
| chr16:81240631
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0147others(66): Show | 72 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.64+1659G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240631 | ||||||
| chr16:81240780
|
G | C | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+1808G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240780 | ||||||
| chr16:81240836
|
A | AT | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(371): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.64+1879dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81240836 | |||||
| chr16:81240836
|
A | ATT | 6 | a0001c0001t0002g0390a0001c0002t0001g0016a0001c0002t0001g0017others(3): Show | 6 | HG00558.hp2 HG01099.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+1878_64+1879dup others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81240836 | |||||
| chr16:81240871
|
G | A | 1 | a0009c0021t0001g0391 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64+1899G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240871 | ||||||
| chr16:81240904
|
G | T | 47 | a0001c0002t0001g0003a0001c0002t0001g0123a0001c0002t0001g0124others(44): Show | 49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.64+1932G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240904 | ||||||
| chr16:81240973
|
G | T | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2001G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81240973 | ||||||
| chr16:81241017
|
T | A | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2045T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241017 | ||||||
| chr16:81241045
|
G | C | 1 | a0002c0004t0001g0032 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.64+2073G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241045 | ||||||
| chr16:81241052
|
G | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01106.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.64+2080G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241052 | ||||||
| chr16:81241054
|
A | G | 150 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(147): Show | 152 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.64+2082A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241054 | ||||||
| chr16:81241080
|
C | A | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2108C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241080 | ||||||
| chr16:81241081
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64+2109G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241081 | ||||||
| chr16:81241095
|
G | A | 1 | a0002c0006t0001g0238 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.64+2123G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241095 | ||||||
| chr16:81241114
|
G | A | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2142G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241114 | ||||||
| chr16:81241175
|
A | G | 19 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(16): Show | 19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+2203A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241175 | ||||||
| chr16:81241200
|
G | C | 1 | a0003c0003t0001g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.64+2228G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241200 | ||||||
| chr16:81241215
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.64+2243G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241215 | ||||||
| chr16:81241228
|
A | G | 19 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(16): Show | 19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+2256A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241228 | ||||||
| chr16:81241268
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64+2296G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241268 | ||||||
| chr16:81241277
|
T | C | 147 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(144): Show | 149 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.64+2305T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241277 | ||||||
| chr16:81241346
|
C | A | 2 | a0001c0002t0001g0016a0001c0002t0001g0017 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.64+2374C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241346 | ||||||
| chr16:81241417
|
T | A | 1 | a0002c0006t0001g0243 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64+2445T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241417 | ||||||
| chr16:81241444
|
G | A | 10 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+2472G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241444 | ||||||
| chr16:81241454
|
G | A | 19 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(16): Show | 19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+2482G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241454 | ||||||
| chr16:81241504
|
C | T | 19 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(16): Show | 19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+2532C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241504 | ||||||
| chr16:81241583
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2611G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241583 | ||||||
| chr16:81241629
|
C | G | 3 | a0001c0005t0001g0030a0001c0005t0001g0031a0008c0013t0001g0029 | 3 | HG01884.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.64+2657C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241629 | ||||||
| chr16:81241663
|
C | A | 128 | a0001c0002t0001g0003a0001c0002t0001g0036a0001c0002t0001g0037others(125): Show | 130 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.64+2691C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241663 | ||||||
| chr16:81241668
|
T | C | 5 | a0001c0005t0001g0012a0001c0005t0001g0013a0002c0004t0001g0009others(2): Show | 5 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2696T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241668 | ||||||
| chr16:81241677
|
G | C | 147 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(144): Show | 149 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.64+2705G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241677 | ||||||
| chr16:81241796
|
A | G | 159 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(156): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.64+2824A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241796 | ||||||
| chr16:81241811
|
A | G | 152 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(149): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.64+2839A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241811 | ||||||
| chr16:81241852
|
A | G | 5 | a0001c0005t0001g0012a0001c0005t0001g0013a0002c0004t0001g0009others(2): Show | 5 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2880A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241852 | ||||||
| chr16:81241854
|
G | A | 2 | a0001c0005t0001g0111a0001c0005t0001g0112 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.64+2882G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241854 | ||||||
| chr16:81241865
|
T | G | 133 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(130): Show | 135 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.64+2893T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81241865 | ||||||
| chr16:81242143
|
T | A | 1 | a0001c0005t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+3171T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242143 | ||||||
| chr16:81242150
|
C | T | 3 | a0002c0004t0001g0108a0002c0004t0001g0109a0002c0004t0001g0110 | 3 | HG00323.hp1 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.64+3178C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242150 | ||||||
| chr16:81242192
|
C | CT | 34 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(31): Show | 35 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.64+3245dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | |||||
| chr16:81242192
|
CT | C | 131 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0244others(128): Show | 133 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.64+3245delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | |||||
| chr16:81242192
|
CTT | C | 18 | a0001c0001t0001g0164a0001c0002t0001g0042a0001c0002t0001g0043others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.64+3244_64+3245del others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | |||||
| chr16:81242192
|
CTTTTTTT | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0178others(8): Show | 13 | HG02027.hp1 NA18612.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+3239_64+3245del others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | |||||
| chr16:81242192
|
CTTTTTTT others(5): Show |
C | 3 | a0002c0006t0001g0364a0003c0003t0001g0363a0003c0003t0001g0365 | 3 | NA18990.hp1 NA18993.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.64+3234_64+3245del others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81242192 | |||||
| chr16:81242239
|
G | A | 2 | a0001c0005t0001g0030a0001c0005t0001g0031 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.65-3236G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242239 | ||||||
| chr16:81242261
|
G | A | 1 | a0001c0005t0001g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.65-3214G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242261 | ||||||
| chr16:81242370
|
T | G | 6 | a0002c0006t0001g0186a0002c0006t0001g0243a0002c0006t0001g0248others(3): Show | 6 | HG00140.hp1 HG01346.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-3105T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242370 | ||||||
| chr16:81242391
|
G | A | 147 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(144): Show | 149 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.65-3084G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242391 | ||||||
| chr16:81242445
|
T | C | 159 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(156): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.65-3030T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242445 | ||||||
| chr16:81242461
|
C | A | 1 | a0001c0001t0001g0165 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.65-3014C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242461 | ||||||
| chr16:81242466
|
G | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0178others(9): Show | 14 | HG02027.hp1 NA18612.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-3009G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242466 | ||||||
| chr16:81242493
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.65-2982G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242493 | ||||||
| chr16:81242505
|
T | G | 2 | a0001c0005t0001g0030a0001c0005t0001g0031 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.65-2970T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242505 | ||||||
| chr16:81242583
|
A | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2892A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242583 | ||||||
| chr16:81242714
|
T | A | 142 | a0001c0002t0001g0003a0001c0002t0001g0036a0001c0002t0001g0037others(139): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.65-2761T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242714 | ||||||
| chr16:81242794
|
C | T | 9 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(6): Show | 9 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-2681C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242794 | ||||||
| chr16:81242824
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.65-2651C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242824 | ||||||
| chr16:81242859
|
G | A | 12 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0254others(9): Show | 12 | HG01175.hp2 HG02080.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-2616G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242859 | ||||||
| chr16:81242938
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2537G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81242938 | ||||||
| chr16:81243003
|
G | C | 1 | a0003c0003t0001g0228 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.65-2472G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243003 | ||||||
| chr16:81243038
|
A | T | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.65-2437A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243038 | ||||||
| chr16:81243127
|
G | T | 129 | a0001c0002t0001g0003a0001c0002t0001g0036a0001c0002t0001g0037others(126): Show | 131 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.65-2348G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243127 | ||||||
| chr16:81243171
|
G | A | 1 | a0001c0002t0001g0046 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.65-2304G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243171 | ||||||
| chr16:81243176
|
A | G | 130 | a0001c0002t0001g0003a0001c0002t0001g0036a0001c0002t0001g0037others(127): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.65-2299A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243176 | ||||||
| chr16:81243203
|
C | T | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.65-2272C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243203 | ||||||
| chr16:81243210
|
T | C | 130 | a0001c0002t0001g0003a0001c0002t0001g0036a0001c0002t0001g0037others(127): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.65-2265T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243210 | ||||||
| chr16:81243246
|
A | G | 65 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0240others(62): Show | 67 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.65-2229A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243246 | ||||||
| chr16:81243454
|
A | ATCAT | 22 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0002t0001g0014others(19): Show | 23 | HG00735.hp1 HG01070.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-1995_65-1992dup others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81243454 | |||||
| chr16:81243454
|
A | ATCATTCA others(1): Show |
113 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(110): Show | 114 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.65-1999_65-1992dup others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81243454 | |||||
| chr16:81243454
|
A | ATCATTCA others(5): Show |
22 | a0001c0002t0001g0003a0001c0002t0001g0049a0001c0002t0001g0358others(19): Show | 23 | HG00323.hp1 HG00733.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-2003_65-1992dup others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81243454 | |||||
| chr16:81243454
|
A | ATCATTCA others(9): Show |
2 | a0001c0005t0001g0020a0001c0005t0001g0021 | 2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.65-2007_65-1992dup others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81243454 | |||||
| chr16:81243564
|
G | A | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1911G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243564 | ||||||
| chr16:81243574
|
T | C | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.65-1901T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243574 | ||||||
| chr16:81243578
|
C | T | 2 | a0002c0004t0001g0141a0002c0004t0001g0142 | 2 | HG01081.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.65-1897C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243578 | ||||||
| chr16:81243582
|
T | C | 158 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(155): Show | 160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.65-1893T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243582 | ||||||
| chr16:81243658
|
G | A | 3 | a0002c0004t0001g0050a0002c0004t0001g0051a0003c0009t0001g0052 | 3 | NA18940.hp2 NA18973.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.65-1817G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243658 | ||||||
| chr16:81243720
|
C | T | 2 | a0001c0001t0001g0361a0001c0001t0001g0362 | 2 | HG00621.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.65-1755C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243720 | ||||||
| chr16:81243906
|
G | A | 1 | a0001c0002t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.65-1569G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81243906 | ||||||
| chr16:81244032
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0178others(9): Show | 14 | HG02027.hp1 NA18612.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-1443C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244032 | ||||||
| chr16:81244137
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-1338G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244137 | ||||||
| chr16:81244179
|
G | A | 149 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(146): Show | 151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.65-1296G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244179 | ||||||
| chr16:81244219
|
A | C | 5 | a0001c0005t0001g0012a0001c0005t0001g0013a0002c0004t0001g0009others(2): Show | 5 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-1256A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244219 | ||||||
| chr16:81244255
|
C | G | 152 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(149): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.65-1220C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244255 | ||||||
| chr16:81244299
|
C | G | 149 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(146): Show | 151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.65-1176C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244299 | ||||||
| chr16:81244355
|
A | G | 128 | a0001c0002t0001g0003a0001c0002t0001g0036a0001c0002t0001g0037others(125): Show | 130 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.65-1120A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244355 | ||||||
| chr16:81244407
|
T | TAAAAAAT others(307): Show |
5 | a0002c0006t0001g0150a0002c0006t0001g0238a0002c0006t0001g0314others(2): Show | 5 | HG01074.hp1 HG02300.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-1058_65-1057ins others(314): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244407 | |||||
| chr16:81244407
|
T | TAAAAAAT others(308): Show |
3 | a0002c0006t0001g0311a0002c0006t0001g0312a0005c0010t0001g0343 | 3 | HG00099.hp2 HG01255.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.65-1058_65-1057ins others(315): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244407 | |||||
| chr16:81244407
|
T | TAAAAAAT others(309): Show |
2 | a0002c0006t0001g0310a0002c0006t0001g0389 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.65-1058_65-1057ins others(316): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244407 | |||||
| chr16:81244533
|
T | C | 152 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(149): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.65-942T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244533 | ||||||
| chr16:81244623
|
T | C | 153 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(150): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.65-852T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244623 | ||||||
| chr16:81244635
|
C | G | 9 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(6): Show | 9 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-840C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244635 | ||||||
| chr16:81244660
|
C | T | 153 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(150): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.65-815C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244660 | ||||||
| chr16:81244661
|
G | A | 1 | a0005c0024t0001g0384 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.65-814G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244661 | ||||||
| chr16:81244706
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-769G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244706 | ||||||
| chr16:81244717
|
C | CT | 19 | a0001c0001t0001g0308a0001c0001t0001g0341a0001c0001t0001g0342others(16): Show | 19 | HG00738.hp2 HG01167.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.65-739dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244717 | |||||
| chr16:81244717
|
C | CTT | 118 | a0001c0002t0001g0003a0001c0002t0001g0037a0001c0002t0001g0038others(115): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.65-740_65-739dupTT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244717 | |||||
| chr16:81244717
|
C | CTTT | 14 | a0001c0002t0001g0014a0001c0002t0001g0045a0001c0002t0001g0100others(11): Show | 14 | HG00733.hp1 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-741_65-739dupTT others(1): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244717 | |||||
| chr16:81244717
|
CT | C | 20 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0189others(17): Show | 20 | HG00639.hp1 HG00673.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.65-739delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81244717 | |||||
| chr16:81244737
|
A | T | 1 | a0002c0004t0001g0099 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.65-738A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244737 | ||||||
| chr16:81244739
|
T | A | 1 | a0002c0004t0001g0099 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.65-736T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244739 | ||||||
| chr16:81244752
|
G | A | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-723G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244752 | ||||||
| chr16:81244767
|
C | A | 1 | a0001c0001t0001g0192 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.65-708C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244767 | ||||||
| chr16:81244894
|
T | G | 3 | a0001c0001t0001g0252a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | NA18966.hp1 NA18973.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.65-581T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244894 | ||||||
| chr16:81244900
|
G | T | 1 | a0001c0001t0001g0147 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.65-575G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244900 | ||||||
| chr16:81244913
|
A | G | 3 | a0001c0002t0001g0149a0001c0005t0001g0031a0008c0013t0001g0029 | 3 | HG02280.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.65-562A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244913 | ||||||
| chr16:81244915
|
A | T | 1 | a0003c0003t0001g0228 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.65-560A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244915 | ||||||
| chr16:81244920
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG00558.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.65-555C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244920 | ||||||
| chr16:81244921
|
G | A | 3 | a0001c0002t0001g0149a0001c0005t0001g0031a0008c0013t0001g0029 | 3 | HG02280.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.65-554G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244921 | ||||||
| chr16:81244956
|
T | A | 153 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(150): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.65-519T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244956 | ||||||
| chr16:81244961
|
G | A | 153 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(150): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.65-514G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244961 | ||||||
| chr16:81244965
|
G | A | 150 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(147): Show | 152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.65-510G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81244965 | ||||||
| chr16:81245013
|
C | T | 153 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(150): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.65-462C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245013 | ||||||
| chr16:81245015
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.65-460C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245015 | ||||||
| chr16:81245016
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-459G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245016 | ||||||
| chr16:81245079
|
G | A | 3 | a0001c0002t0001g0149a0001c0005t0001g0031a0008c0013t0001g0029 | 3 | HG02280.hp2 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.65-396G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245079 | ||||||
| chr16:81245118
|
C | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0178a0001c0001t0001g0179others(8): Show | 13 | HG02027.hp1 NA18612.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-357C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245118 | ||||||
| chr16:81245258
|
A | G | 1 | a0002c0006t0001g0186 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.65-217A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245258 | ||||||
| chr16:81245446
|
G | A | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.65-29G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 1/10 | chr16 | 81245446 | ||||||
| chr16:81245773
|
C | G | 153 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(150): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.193+170C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245773 | ||||||
| chr16:81245829
|
A | G | 154 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(151): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.193+226A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245829 | ||||||
| chr16:81245849
|
C | CT | 125 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(122): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.193+272dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | |||||
| chr16:81245849
|
C | CTT | 16 | a0001c0001t0001g0008a0001c0001t0001g0185a0001c0001t0001g0225others(13): Show | 17 | HG01169.hp1 HG01175.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.193+271_193+272dup others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | |||||
| chr16:81245849
|
CTTTTTT | C | 120 | a0001c0002t0001g0003a0001c0002t0001g0036a0001c0002t0001g0037others(117): Show | 122 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.193+267_193+272del others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | |||||
| chr16:81245849
|
CTTTTTTT | C | 6 | a0001c0002t0001g0056a0001c0005t0001g0118a0001c0005t0001g0119others(3): Show | 6 | HG00609.hp1 HG01243.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+266_193+272del others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | |||||
| chr16:81245849
|
CTTTTTTT others(1): Show |
C | 19 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(16): Show | 19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.193+265_193+272del others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | |||||
| chr16:81245849
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+263_193+272del others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245849 | |||||
| chr16:81245877
|
T | C | 152 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0015others(149): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.193+274T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245877 | ||||||
| chr16:81245917
|
C | CA | 3 | a0002c0006t0001g0245a0003c0003t0001g0007a0003c0003t0001g0309 | 4 | HG01167.hp1 HG01256.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+316dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81245917 | |||||
| chr16:81245920
|
T | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+317T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245920 | ||||||
| chr16:81245958
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.193+355G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245958 | ||||||
| chr16:81245982
|
C | G | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+379C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81245982 | ||||||
| chr16:81246075
|
C | G | 129 | a0001c0002t0001g0003a0001c0002t0001g0036a0001c0002t0001g0037others(126): Show | 131 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.193+472C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246075 | ||||||
| chr16:81246080
|
C | T | 4 | a0001c0001t0001g0252a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | NA18955.hp2 NA18966.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+477C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246080 | ||||||
| chr16:81246211
|
C | G | 1 | a0001c0001t0001g0356 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.193+608C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246211 | ||||||
| chr16:81246260
|
G | A | 10 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(7): Show | 10 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+657G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246260 | ||||||
| chr16:81246275
|
A | G | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0003c0003t0001g0301others(1): Show | 4 | HG02155.hp2 NA18943.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+672A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246275 | ||||||
| chr16:81246335
|
T | C | 46 | a0001c0001t0001g0221a0001c0001t0001g0247a0001c0001t0001g0252others(43): Show | 46 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.193+732T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246335 | ||||||
| chr16:81246412
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.193+809G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246412 | ||||||
| chr16:81246418
|
A | G | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+815A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246418 | ||||||
| chr16:81246453
|
T | G | 1 | a0001c0001t0001g0318 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.193+850T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246453 | ||||||
| chr16:81246611
|
GA | G | 134 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.193+1009delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246611 | ||||||
| chr16:81246641
|
G | A | 1 | a0002c0006t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.193+1038G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246641 | ||||||
| chr16:81246758
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.193+1155C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246758 | ||||||
| chr16:81246842
|
C | T | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+1239C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246842 | ||||||
| chr16:81246850
|
C | CA | 10 | a0001c0001t0001g0147a0001c0001t0001g0193a0001c0001t0001g0229others(7): Show | 10 | HG01981.hp1 HG02280.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+1265dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAA | 55 | a0001c0002t0001g0003a0001c0002t0001g0056a0001c0002t0001g0123others(52): Show | 57 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.193+1263_193+1265d others(5): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAAAAAA others(3): Show |
6 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(3): Show | 6 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+1256_193+1265d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAAAAAA others(4): Show |
1 | a0006c0016t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.193+1255_193+1265d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAAAAAA others(5): Show |
1 | a0001c0005t0001g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193+1254_193+1265d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAAAAAA others(6): Show |
1 | a0002c0004t0001g0103 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.193+1253_193+1265d others(15): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAAAAAA others(7): Show |
17 | a0001c0005t0001g0091a0002c0004t0001g0035a0002c0004t0001g0044others(14): Show | 17 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+1252_193+1265d others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAAAAAA others(8): Show |
25 | a0001c0001t0001g0255a0001c0002t0001g0036a0001c0002t0001g0043others(22): Show | 25 | HG00323.hp1 HG00609.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.193+1251_193+1265d others(17): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAAAAAA others(9): Show |
26 | a0001c0002t0001g0037a0001c0002t0001g0038a0001c0002t0001g0042others(23): Show | 26 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.193+1250_193+1265d others(18): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAAAAAA others(10): Show |
6 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0061others(3): Show | 6 | HG00438.hp1 HG01433.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+1249_193+1265d others(19): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0001g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.193+1265_193+1266i others(21): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
CA | C | 15 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(12): Show | 15 | HG00280.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.193+1265delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246850
|
CAA | C | 8 | a0001c0005t0001g0022a0001c0005t0001g0023a0001c0005t0001g0024others(5): Show | 8 | HG00733.hp1 HG01168.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+1264_193+1265d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81246850 | |||||
| chr16:81246866
|
A | G | 2 | a0001c0001t0001g0355a0003c0003t0001g0354 | 2 | HG00733.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.193+1263A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246866 | ||||||
| chr16:81246869
|
G | A | 134 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.193+1266G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246869 | ||||||
| chr16:81246982
|
A | C | 151 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.193+1379A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81246982 | ||||||
| chr16:81247008
|
C | T | 8 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(5): Show | 8 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+1405C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247008 | ||||||
| chr16:81247009
|
G | A | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.193+1406G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247009 | ||||||
| chr16:81247028
|
C | G | 1 | a0001c0005t0001g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.193+1425C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247028 | ||||||
| chr16:81247095
|
A | G | 140 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0016others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.193+1492A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247095 | ||||||
| chr16:81247216
|
G | A | 6 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0269others(3): Show | 6 | HG01081.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+1613G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247216 | ||||||
| chr16:81247250
|
C | T | 3 | a0001c0005t0001g0012a0001c0005t0001g0013a0006c0016t0001g0010 | 3 | HG02559.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.193+1647C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247250 | ||||||
| chr16:81247251
|
TCA | T | 5 | a0003c0003t0001g0334a0003c0003t0001g0335a0003c0003t0001g0336others(2): Show | 5 | HG02015.hp2 HG02040.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+1649_193+1650d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247251 | ||||||
| chr16:81247275
|
G | C | 8 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(5): Show | 8 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+1672G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247275 | ||||||
| chr16:81247292
|
T | G | 138 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.193+1689T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247292 | ||||||
| chr16:81247355
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG00558.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.193+1752T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247355 | ||||||
| chr16:81247427
|
C | T | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.193+1824C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247427 | ||||||
| chr16:81247440
|
G | A | 7 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(4): Show | 7 | HG02055.hp2 HG03098.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+1837G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247440 | ||||||
| chr16:81247468
|
A | T | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.193+1865A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247468 | ||||||
| chr16:81247532
|
A | G | 1 | a0002c0006t0001g0150 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.193+1929A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247532 | ||||||
| chr16:81247557
|
G | T | 2 | a0001c0005t0001g0136a0001c0005t0001g0137 | 2 | HG01433.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.193+1954G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247557 | ||||||
| chr16:81247651
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.193+2048C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247651 | ||||||
| chr16:81247783
|
C | T | 1 | a0001c0007t0001g0148 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193+2180C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247783 | ||||||
| chr16:81247822
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+2219G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247822 | ||||||
| chr16:81247852
|
T | A | 1 | a0001c0005t0001g0022 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.193+2249T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247852 | ||||||
| chr16:81247881
|
C | CCCACCAT | 12 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(9): Show | 12 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.193+2279_193+2280i others(9): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81247881 | |||||
| chr16:81247937
|
C | G | 1 | a0002c0004t0001g0110 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.193+2334C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247937 | ||||||
| chr16:81247978
|
T | G | 43 | a0001c0002t0001g0063a0001c0002t0001g0083a0001c0002t0001g0107others(40): Show | 43 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.193+2375T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81247978 | ||||||
| chr16:81248008
|
G | A | 1 | a0013c0019t0001g0188 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.193+2405G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248008 | ||||||
| chr16:81248040
|
A | T | 1 | a0001c0001t0001g0284 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193+2437A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248040 | ||||||
| chr16:81248264
|
G | A | 1 | a0001c0001t0001g0347 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.193+2661G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248264 | ||||||
| chr16:81248287
|
C | G | 1 | a0001c0002t0001g0077 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.193+2684C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248287 | ||||||
| chr16:81248337
|
C | A | 160 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.193+2734C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248337 | ||||||
| chr16:81248357
|
T | C | 149 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.193+2754T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248357 | ||||||
| chr16:81248366
|
G | A | 145 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.193+2763G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248366 | ||||||
| chr16:81248390
|
C | T | 160 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.193+2787C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248390 | ||||||
| chr16:81248405
|
C | CA | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(196): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.193+2823dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | |||||
| chr16:81248405
|
C | CAA | 145 | a0001c0001t0001g0040a0001c0001t0001g0160a0001c0001t0001g0161others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.193+2822_193+2823d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | |||||
| chr16:81248405
|
C | CAAA | 20 | a0001c0002t0001g0056a0001c0002t0001g0067a0001c0002t0001g0068others(17): Show | 20 | HG01243.hp1 HG01361.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.193+2821_193+2823d others(5): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | |||||
| chr16:81248405
|
C | CAAAAAAA others(1): Show |
8 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(5): Show | 8 | HG00280.hp2 HG01074.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+2816_193+2823d others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | |||||
| chr16:81248405
|
C | CAAAAAAA others(3): Show |
2 | a0001c0005t0001g0027a0001c0005t0001g0031 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.193+2814_193+2823d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | |||||
| chr16:81248405
|
C | CAAAAAAA others(5): Show |
1 | a0002c0006t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.193+2812_193+2823d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | |||||
| chr16:81248405
|
C | CAAAAAAA others(8): Show |
1 | a0001c0002t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.193+2809_193+2823d others(17): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | |||||
| chr16:81248405
|
C | CAAAAAAA others(10): Show |
4 | a0001c0002t0001g0014a0001c0005t0001g0012a0001c0005t0001g0013others(1): Show | 4 | HG02559.hp2 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+2807_193+2823d others(19): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | |||||
| chr16:81248405
|
C | CAAAAAAA others(16): Show |
2 | a0002c0004t0001g0009a0002c0004t0001g0011 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.193+2823_193+2824i others(25): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81248405 | |||||
| chr16:81248499
|
G | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+2896G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248499 | ||||||
| chr16:81248591
|
A | C | 160 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.193+2988A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248591 | ||||||
| chr16:81248663
|
T | C | 160 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.193+3060T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248663 | ||||||
| chr16:81248688
|
C | T | 160 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.193+3085C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248688 | ||||||
| chr16:81248690
|
G | T | 136 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.193+3087G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248690 | ||||||
| chr16:81248747
|
C | G | 1 | a0001c0002t0001g0077 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.193+3144C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248747 | ||||||
| chr16:81248774
|
A | G | 160 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.193+3171A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248774 | ||||||
| chr16:81248778
|
A | G | 160 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(157): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.193+3175A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248778 | ||||||
| chr16:81248801
|
C | T | 1 | a0001c0005t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.193+3198C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248801 | ||||||
| chr16:81248869
|
G | A | 12 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(9): Show | 12 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.193+3266G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248869 | ||||||
| chr16:81248938
|
A | G | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3335A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248938 | ||||||
| chr16:81248986
|
T | G | 12 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(9): Show | 12 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.193+3383T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81248986 | ||||||
| chr16:81249006
|
C | T | 12 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(9): Show | 12 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.193+3403C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249006 | ||||||
| chr16:81249049
|
C | A | 165 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.193+3446C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249049 | ||||||
| chr16:81249092
|
C | CTT | 12 | a0001c0002t0001g0123a0001c0005t0001g0020a0001c0005t0001g0021others(9): Show | 12 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.193+3504_193+3505d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249092 | |||||
| chr16:81249092
|
C | CTTT | 132 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.193+3503_193+3505d others(5): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249092 | |||||
| chr16:81249092
|
CT | C | 17 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0175others(14): Show | 17 | HG00323.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.193+3505delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249092 | |||||
| chr16:81249112
|
A | ATGGAGTC others(18): Show |
1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193+3516_193+3540d others(27): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249112 | |||||
| chr16:81249215
|
G | T | 162 | a0001c0001t0001g0008a0001c0001t0001g0255a0001c0002t0001g0003others(159): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.193+3612G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249215 | ||||||
| chr16:81249238
|
A | G | 1 | a0001c0005t0001g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.193+3635A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249238 | ||||||
| chr16:81249239
|
T | C | 2 | a0001c0001t0001g0379a0001c0001t0001g0380 | 2 | HG01192.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.193+3636T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249239 | ||||||
| chr16:81249243
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3640A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249243 | ||||||
| chr16:81249257
|
G | GT | 8 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0005t0001g0012others(5): Show | 8 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+3663dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249257 | |||||
| chr16:81249267
|
C | CT | 5 | a0001c0001t0001g0008a0001c0002t0001g0083a0004c0008t0001g0054others(2): Show | 6 | HG00738.hp2 HG00741.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+3671dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81249267 | |||||
| chr16:81249336
|
A | G | 155 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.193+3733A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249336 | ||||||
| chr16:81249393
|
A | G | 3 | a0001c0005t0001g0114a0001c0005t0001g0116a0001c0005t0001g0117 | 3 | HG00639.hp2 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193+3790A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249393 | ||||||
| chr16:81249423
|
A | T | 1 | a0001c0005t0001g0156 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.193+3820A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249423 | ||||||
| chr16:81249458
|
G | A | 1 | a0003c0003t0001g0340 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.193+3855G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249458 | ||||||
| chr16:81249481
|
C | T | 1 | a0003c0003t0001g0251 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.193+3878C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249481 | ||||||
| chr16:81249502
|
C | T | 1 | a0001c0002t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193+3899C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249502 | ||||||
| chr16:81249519
|
A | G | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0229others(1): Show | 4 | HG01978.hp1 HG01981.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3916A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249519 | ||||||
| chr16:81249551
|
C | T | 1 | a0001c0005t0001g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193+3948C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249551 | ||||||
| chr16:81249552
|
G | A | 1 | a0003c0003t0001g0346 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.193+3949G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249552 | ||||||
| chr16:81249575
|
T | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+3972T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249575 | ||||||
| chr16:81249592
|
G | C | 1 | a0002c0004t0001g0099 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.193+3989G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249592 | ||||||
| chr16:81249595
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.193+3992T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249595 | ||||||
| chr16:81249614
|
C | T | 3 | a0001c0001t0001g0197a0001c0018t0001g0276a0013c0019t0001g0188 | 3 | HG00735.hp2 HG03239.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.193+4011C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249614 | ||||||
| chr16:81249692
|
C | T | 5 | a0002c0004t0001g0055a0002c0004t0001g0065a0002c0004t0001g0078others(2): Show | 5 | HG00609.hp1 HG02129.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+4089C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249692 | ||||||
| chr16:81249701
|
G | A | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+4098G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249701 | ||||||
| chr16:81249706
|
A | G | 1 | a0003c0003t0001g0332 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.193+4103A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249706 | ||||||
| chr16:81249717
|
C | T | 157 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.193+4114C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249717 | ||||||
| chr16:81249727
|
T | C | 157 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0014others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.193+4124T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249727 | ||||||
| chr16:81249784
|
C | A | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+4181C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249784 | ||||||
| chr16:81249800
|
G | C | 1 | a0002c0004t0001g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.193+4197G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249800 | ||||||
| chr16:81249839
|
G | T | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+4236G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249839 | ||||||
| chr16:81249971
|
G | A | 1 | a0002c0004t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.193+4368G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249971 | ||||||
| chr16:81249993
|
A | G | 156 | a0001c0001t0001g0255a0001c0001t0001g0347a0001c0002t0001g0003others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.193+4390A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81249993 | ||||||
| chr16:81250022
|
C | T | 1 | a0003c0003t0001g0007 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.193+4419C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250022 | ||||||
| chr16:81250025
|
A | G | 6 | a0001c0002t0001g0014a0001c0005t0001g0012a0001c0005t0001g0013others(3): Show | 6 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+4422A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250025 | ||||||
| chr16:81250026
|
G | A | 143 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.193+4423G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250026 | ||||||
| chr16:81250032
|
C | A | 7 | a0001c0002t0001g0014a0001c0005t0001g0012a0001c0005t0001g0013others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+4429C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250032 | ||||||
| chr16:81250101
|
C | T | 7 | a0001c0002t0001g0014a0001c0005t0001g0012a0001c0005t0001g0013others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+4498C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250101 | ||||||
| chr16:81250124
|
G | A | 2 | a0001c0001t0001g0231a0003c0003t0001g0200 | 2 | NA18969.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.193+4521G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250124 | ||||||
| chr16:81250224
|
C | G | 155 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0255others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.193+4621C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250224 | ||||||
| chr16:81250234
|
G | A | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.193+4631G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250234 | ||||||
| chr16:81250237
|
G | A | 132 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.193+4634G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250237 | ||||||
| chr16:81250460
|
C | G | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+4857C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250460 | ||||||
| chr16:81250470
|
C | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG03017.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.193+4867C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250470 | ||||||
| chr16:81250492
|
C | T | 1 | a0002c0006t0001g0378 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.193+4889C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250492 | ||||||
| chr16:81250578
|
C | CT | 133 | a0001c0001t0001g0193a0001c0001t0001g0230a0001c0001t0001g0237others(130): Show | 136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.193+4995dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | |||||
| chr16:81250578
|
C | CTT | 11 | a0001c0001t0001g0218a0001c0002t0001g0135a0001c0005t0001g0121others(8): Show | 11 | HG00099.hp2 HG00741.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+4994_193+4995d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | |||||
| chr16:81250578
|
C | CTTTTTTT others(4): Show |
8 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(5): Show | 8 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+4985_193+4995d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | |||||
| chr16:81250578
|
C | CTTTTTTT others(5): Show |
1 | a0001c0005t0001g0025 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.193+4984_193+4995d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | |||||
| chr16:81250578
|
CT | C | 14 | a0001c0001t0001g0226a0001c0001t0001g0270a0001c0001t0001g0271others(11): Show | 14 | HG00323.hp2 HG00558.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.193+4995delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81250578 | |||||
| chr16:81250697
|
C | T | 7 | a0001c0002t0001g0014a0001c0005t0001g0012a0001c0005t0001g0013others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+5094C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250697 | ||||||
| chr16:81250773
|
G | T | 2 | a0003c0003t0001g0346a0003c0003t0001g0351 | 2 | HG01943.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.193+5170G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250773 | ||||||
| chr16:81250800
|
C | T | 2 | a0001c0001t0001g0217a0003c0003t0001g0158 | 2 | HG02074.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.193+5197C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250800 | ||||||
| chr16:81250868
|
A | C | 1 | a0002c0004t0001g0099 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.193+5265A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250868 | ||||||
| chr16:81250871
|
G | A | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.193+5268G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250871 | ||||||
| chr16:81250979
|
C | T | 1 | a0001c0001t0001g0288 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193+5376C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81250979 | ||||||
| chr16:81251062
|
T | C | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+5459T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251062 | ||||||
| chr16:81251132
|
C | A | 1 | a0001c0001t0001g0288 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193+5529C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251132 | ||||||
| chr16:81251169
|
C | T | 6 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0269others(3): Show | 6 | HG01081.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+5566C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251169 | ||||||
| chr16:81251220
|
T | C | 1 | a0001c0001t0001g0366 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.193+5617T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251220 | ||||||
| chr16:81251414
|
T | G | 107 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.193+5811T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251414 | ||||||
| chr16:81251502
|
G | C | 53 | a0001c0001t0001g0221a0001c0001t0001g0247a0001c0001t0001g0252others(50): Show | 53 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.193+5899G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251502 | ||||||
| chr16:81251521
|
C | G | 1 | a0003c0003t0001g0228 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.193+5918C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251521 | ||||||
| chr16:81251695
|
G | C | 1 | a0003c0003t0001g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.193+6092G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251695 | ||||||
| chr16:81251709
|
C | T | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6106C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251709 | ||||||
| chr16:81251836
|
A | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6233A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251836 | ||||||
| chr16:81251838
|
A | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6235A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251838 | ||||||
| chr16:81251851
|
C | T | 1 | a0002c0004t0001g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.193+6248C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251851 | ||||||
| chr16:81251852
|
GCA | G | 3 | a0002c0006t0001g0028a0002c0006t0001g0173a0002c0020t0001g0275 | 3 | HG02055.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.193+6266_193+6267d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251852 | |||||
| chr16:81251859
|
C | A | 1 | a0001c0001t0001g0356 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.193+6256C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251859 | ||||||
| chr16:81251869
|
C | T | 15 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0002t0001g0014others(12): Show | 15 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.193+6266C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251869 | ||||||
| chr16:81251871
|
T | C | 1 | a0001c0007t0001g0235 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193+6268T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251871 | ||||||
| chr16:81251872
|
A | ATGTGTGT others(1): Show |
3 | a0001c0007t0001g0162a0002c0006t0001g0163a0012c0012t0001g0152 | 3 | HG03098.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.193+6270_193+6271i others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | |||||
| chr16:81251872
|
A | ATGTGTGT others(3): Show |
1 | a0001c0002t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193+6270_193+6271i others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | |||||
| chr16:81251872
|
A | ATGTGTGT others(5): Show |
4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6270_193+6271i others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | |||||
| chr16:81251872
|
A | ATGTGTGT others(7): Show |
3 | a0001c0005t0001g0012a0001c0005t0001g0013a0006c0016t0001g0010 | 3 | HG02559.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.193+6270_193+6271i others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | |||||
| chr16:81251872
|
A | ATGTGTGT others(9): Show |
2 | a0002c0004t0001g0009a0002c0004t0001g0011 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.193+6270_193+6271i others(18): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | |||||
| chr16:81251872
|
A | ATGTGTGT others(15): Show |
1 | a0001c0005t0001g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193+6270_193+6271i others(24): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251872 | |||||
| chr16:81251874
|
A | ATGTG | 34 | a0001c0001t0001g0255a0001c0002t0001g0036a0001c0002t0001g0038others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.193+6285_193+6288d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251874 | |||||
| chr16:81251874
|
A | ATGTGTG | 64 | a0001c0002t0001g0003a0001c0002t0001g0123a0001c0002t0001g0124others(61): Show | 66 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.193+6283_193+6288d others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251874 | |||||
| chr16:81251874
|
A | ATGTGTGT others(3): Show |
2 | a0001c0005t0001g0027a0001c0007t0001g0201 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.193+6279_193+6288d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251874 | |||||
| chr16:81251874
|
A | ATGTGTGT others(5): Show |
1 | a0001c0005t0001g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.193+6277_193+6288d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81251874 | |||||
| chr16:81251874
|
A | G | 17 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0002t0001g0014others(14): Show | 17 | HG00735.hp1 HG01070.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+6271A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251874 | ||||||
| chr16:81251892
|
A | G | 7 | a0001c0001t0001g0164a0001c0002t0001g0015a0001c0002t0001g0149others(4): Show | 8 | HG01257.hp1 HG01258.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+6289A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251892 | ||||||
| chr16:81251894
|
A | G | 1 | a0003c0003t0001g0239 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.193+6291A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251894 | ||||||
| chr16:81251900
|
C | G | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6297C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251900 | ||||||
| chr16:81251978
|
G | A | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | NA18944.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.193+6375G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81251978 | ||||||
| chr16:81252085
|
G | C | 1 | a0001c0005t0001g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+6482G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252085 | ||||||
| chr16:81252195
|
T | A | 1 | a0001c0001t0001g0288 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193+6592T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252195 | ||||||
| chr16:81252204
|
T | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+6601T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252204 | ||||||
| chr16:81252396
|
C | G | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | NA18984.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.193+6793C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252396 | ||||||
| chr16:81252413
|
G | C | 1 | a0001c0005t0001g0022 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.193+6810G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252413 | ||||||
| chr16:81252536
|
G | A | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.193+6933G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252536 | ||||||
| chr16:81252545
|
A | G | 1 | a0001c0001t0001g0382 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.193+6942A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252545 | ||||||
| chr16:81252608
|
G | A | 2 | a0001c0002t0001g0016a0001c0002t0001g0017 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193+7005G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252608 | ||||||
| chr16:81252738
|
G | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-6938G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252738 | ||||||
| chr16:81252745
|
C | G | 8 | a0001c0002t0001g0003a0001c0002t0001g0358a0001c0002t0001g0359others(5): Show | 9 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-6931C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252745 | ||||||
| chr16:81252856
|
T | C | 171 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(168): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.194-6820T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252856 | ||||||
| chr16:81252867
|
A | G | 122 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.194-6809A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252867 | ||||||
| chr16:81252995
|
C | G | 3 | a0002c0006t0001g0028a0002c0006t0001g0173a0002c0020t0001g0275 | 3 | HG02055.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.194-6681C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81252995 | ||||||
| chr16:81253090
|
C | T | 1 | a0001c0002t0002g0034 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.194-6586C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253090 | ||||||
| chr16:81253139
|
C | G | 1 | a0001c0002t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-6537C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253139 | ||||||
| chr16:81253193
|
G | A | 1 | a0002c0004t0001g0065 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.194-6483G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253193 | ||||||
| chr16:81253344
|
C | G | 1 | a0001c0002t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-6332C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253344 | ||||||
| chr16:81253545
|
C | G | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.194-6131C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253545 | ||||||
| chr16:81253840
|
A | G | 122 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.194-5836A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253840 | ||||||
| chr16:81253894
|
T | C | 108 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0255others(105): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.194-5782T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81253894 | ||||||
| chr16:81254037
|
C | G | 14 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(11): Show | 14 | HG00735.hp1 HG01070.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.194-5639C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254037 | ||||||
| chr16:81254171
|
C | G | 4 | a0001c0001t0001g0252a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | NA18955.hp2 NA18966.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-5505C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254171 | ||||||
| chr16:81254185
|
A | G | 1 | a0001c0002t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-5491A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254185 | ||||||
| chr16:81254243
|
C | T | 118 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.194-5433C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254243 | ||||||
| chr16:81254269
|
T | A | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.194-5407T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254269 | ||||||
| chr16:81254270
|
G | A | 10 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0002t0001g0015others(7): Show | 10 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-5406G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254270 | ||||||
| chr16:81254277
|
T | C | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.194-5399T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254277 | ||||||
| chr16:81254289
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.194-5387C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254289 | ||||||
| chr16:81254295
|
A | AT | 166 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0183others(163): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.194-5354dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254295 | |||||
| chr16:81254295
|
A | ATT | 39 | a0001c0001t0001g0230a0001c0001t0001g0234a0001c0001t0001g0247others(36): Show | 39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.194-5355_194-5354d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254295 | |||||
| chr16:81254295
|
AT | A | 6 | a0001c0001t0001g0187a0001c0001t0001g0285a0001c0001t0001g0330others(3): Show | 6 | HG01515.hp2 HG02886.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-5354delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254295 | |||||
| chr16:81254295
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.194-5364_194-5354d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254295 | |||||
| chr16:81254332
|
G | A | 103 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(100): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.194-5344G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254332 | ||||||
| chr16:81254359
|
C | A | 2 | a0001c0001t0001g0385a0001c0001t0001g0386 | 2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.194-5317C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254359 | ||||||
| chr16:81254370
|
C | T | 1 | a0001c0005t0001g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.194-5306C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254370 | ||||||
| chr16:81254426
|
C | G | 1 | a0001c0001t0001g0356 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.194-5250C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254426 | ||||||
| chr16:81254429
|
G | A | 1 | a0001c0007t0001g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.194-5247G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254429 | ||||||
| chr16:81254450
|
A | AT | 9 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0001t0001g0288others(6): Show | 9 | HG00735.hp1 HG01070.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-5213dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254450 | |||||
| chr16:81254450
|
AT | A | 13 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0262others(10): Show | 13 | HG02055.hp2 HG02451.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.194-5213delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81254450 | |||||
| chr16:81254493
|
G | A | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.194-5183G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254493 | ||||||
| chr16:81254537
|
A | G | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.194-5139A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254537 | ||||||
| chr16:81254607
|
A | C | 2 | a0002c0004t0001g0103a0002c0004t0001g0104 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.194-5069A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254607 | ||||||
| chr16:81254671
|
A | G | 2 | a0001c0011t0001g0081a0002c0004t0001g0090 | 2 | HG01361.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.194-5005A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254671 | ||||||
| chr16:81254851
|
C | T | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4825C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254851 | ||||||
| chr16:81254891
|
G | A | 3 | a0001c0005t0001g0027a0001c0005t0001g0151a0001c0007t0001g0201 | 3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.194-4785G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254891 | ||||||
| chr16:81254892
|
G | T | 2 | a0001c0001t0001g0281a0001c0001t0001g0283 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.194-4784G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254892 | ||||||
| chr16:81254915
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.194-4761G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81254915 | ||||||
| chr16:81255058
|
C | T | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4618C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255058 | ||||||
| chr16:81255076
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0203a0001c0001t0001g0225others(1): Show | 5 | HG01071.hp2 HG01261.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-4600C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255076 | ||||||
| chr16:81255117
|
G | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0011 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.194-4559G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255117 | ||||||
| chr16:81255125
|
C | G | 11 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(8): Show | 11 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.194-4551C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255125 | ||||||
| chr16:81255313
|
G | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-4363G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255313 | ||||||
| chr16:81255324
|
C | G | 5 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(2): Show | 5 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-4352C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255324 | ||||||
| chr16:81255493
|
AT | A | 10 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(7): Show | 10 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-4174delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81255493 | |||||
| chr16:81255497
|
T | A | 5 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(2): Show | 5 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-4179T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255497 | ||||||
| chr16:81255509
|
TA | T | 11 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(8): Show | 11 | HG02280.hp2 HG02602.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.194-4166delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255509 | ||||||
| chr16:81255510
|
A | T | 99 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(96): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.194-4166A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255510 | ||||||
| chr16:81255803
|
C | A | 1 | a0002c0020t0001g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.194-3873C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255803 | ||||||
| chr16:81255827
|
T | G | 3 | a0002c0006t0001g0364a0003c0003t0001g0363a0003c0003t0001g0365 | 3 | NA18990.hp1 NA18993.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.194-3849T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255827 | ||||||
| chr16:81255911
|
C | T | 1 | a0001c0001t0002g0375 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.194-3765C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255911 | ||||||
| chr16:81255947
|
G | C | 1 | a0003c0003t0001g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.194-3729G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255947 | ||||||
| chr16:81255967
|
G | C | 118 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(115): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.194-3709G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255967 | ||||||
| chr16:81255979
|
A | AT | 101 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(98): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.194-3689dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81255979 | |||||
| chr16:81255996
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 12 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.194-3680A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81255996 | ||||||
| chr16:81256117
|
A | AT | 35 | a0001c0001t0001g0182a0001c0001t0001g0190a0001c0001t0001g0234others(32): Show | 36 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.194-3546dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81256117 | |||||
| chr16:81256220
|
G | C | 8 | a0001c0002t0001g0015a0001c0005t0001g0027a0001c0005t0001g0151others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-3456G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256220 | ||||||
| chr16:81256255
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0344 | 3 | HG03704.hp2 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.194-3421G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256255 | ||||||
| chr16:81256546
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.194-3130A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256546 | ||||||
| chr16:81256576
|
T | C | 1 | a0001c0002t0001g0059 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.194-3100T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256576 | ||||||
| chr16:81256642
|
C | A | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.194-3034C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256642 | ||||||
| chr16:81256690
|
C | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2986C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256690 | ||||||
| chr16:81256739
|
T | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2937T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256739 | ||||||
| chr16:81256821
|
G | C | 101 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(98): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.194-2855G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256821 | ||||||
| chr16:81256866
|
C | T | 3 | a0001c0005t0001g0027a0001c0005t0001g0151a0001c0007t0001g0201 | 3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.194-2810C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256866 | ||||||
| chr16:81256980
|
C | T | 1 | a0001c0002t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-2696C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256980 | ||||||
| chr16:81256989
|
G | A | 2 | a0001c0001t0001g0164a0001c0002t0001g0149 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.194-2687G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81256989 | ||||||
| chr16:81257000
|
G | A | 98 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.194-2676G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257000 | ||||||
| chr16:81257026
|
T | A | 117 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(114): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.194-2650T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257026 | ||||||
| chr16:81257259
|
C | T | 103 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(100): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.194-2417C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257259 | ||||||
| chr16:81257285
|
G | C | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.194-2391G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257285 | ||||||
| chr16:81257287
|
C | T | 74 | a0001c0001t0001g0255a0001c0002t0001g0003a0001c0002t0001g0036others(71): Show | 75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.194-2389C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257287 | ||||||
| chr16:81257289
|
G | T | 3 | a0001c0002t0001g0003a0001c0002t0001g0358a0001c0002t0001g0359 | 4 | HG01891.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-2387G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257289 | ||||||
| chr16:81257296
|
G | T | 2 | a0001c0001t0001g0382a0001c0001t0001g0393 | 2 | HG01346.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.194-2380G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257296 | ||||||
| chr16:81257299
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.194-2377C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257299 | ||||||
| chr16:81257513
|
C | T | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.194-2163C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257513 | ||||||
| chr16:81257606
|
A | AGGCAAAC others(17): Show |
1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.194-2069_194-2046d others(26): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81257606 | |||||
| chr16:81257674
|
G | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-2002G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257674 | ||||||
| chr16:81257695
|
G | A | 1 | a0002c0004t0001g0064 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.194-1981G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257695 | ||||||
| chr16:81257773
|
G | A | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.194-1903G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257773 | ||||||
| chr16:81257858
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.194-1818T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257858 | ||||||
| chr16:81257872
|
T | G | 1 | a0001c0001t0001g0286 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.194-1804T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257872 | ||||||
| chr16:81257879
|
C | CA | 9 | a0001c0001t0001g0161a0001c0001t0001g0164a0001c0002t0001g0085others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-1780dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81257879 | |||||
| chr16:81257879
|
CA | C | 7 | a0001c0001t0001g0226a0001c0002t0001g0046a0001c0005t0001g0097others(4): Show | 7 | HG00558.hp1 HG01099.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.194-1780delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81257879 | |||||
| chr16:81257928
|
G | A | 1 | a0002c0004t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.194-1748G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257928 | ||||||
| chr16:81257973
|
G | T | 2 | a0001c0007t0001g0162a0002c0006t0001g0163 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.194-1703G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257973 | ||||||
| chr16:81257999
|
C | G | 8 | a0001c0002t0001g0015a0001c0005t0001g0027a0001c0005t0001g0151others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-1677C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81257999 | ||||||
| chr16:81258033
|
G | A | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.194-1643G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258033 | ||||||
| chr16:81258037
|
C | T | 2 | a0001c0001t0001g0382a0001c0001t0001g0393 | 2 | HG01346.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.194-1639C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258037 | ||||||
| chr16:81258124
|
T | C | 1 | a0003c0003t0001g0336 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.194-1552T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258124 | ||||||
| chr16:81258134
|
A | G | 3 | a0001c0005t0001g0027a0001c0005t0001g0151a0001c0007t0001g0201 | 3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.194-1542A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258134 | ||||||
| chr16:81258258
|
C | T | 1 | a0003c0009t0001g0088 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.194-1418C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258258 | ||||||
| chr16:81258290
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-1386G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258290 | ||||||
| chr16:81258416
|
G | A | 1 | a0003c0003t0001g0323 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.194-1260G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258416 | ||||||
| chr16:81258453
|
C | T | 3 | a0001c0005t0001g0027a0001c0005t0001g0151a0001c0007t0001g0201 | 3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.194-1223C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258453 | ||||||
| chr16:81258478
|
T | C | 70 | a0001c0001t0001g0203a0001c0002t0001g0003a0001c0002t0001g0123others(67): Show | 72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.194-1198T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258478 | ||||||
| chr16:81258501
|
G | A | 3 | a0002c0006t0001g0028a0002c0006t0001g0173a0002c0020t0001g0275 | 3 | HG02055.hp2 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.194-1175G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258501 | ||||||
| chr16:81258602
|
G | C | 8 | a0001c0002t0001g0015a0001c0005t0001g0027a0001c0005t0001g0151others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-1074G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258602 | ||||||
| chr16:81258611
|
G | T | 1 | a0001c0002t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.194-1065G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258611 | ||||||
| chr16:81258623
|
T | C | 2 | a0001c0002t0001g0172a0001c0005t0001g0113 | 2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.194-1053T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258623 | ||||||
| chr16:81258782
|
G | C | 1 | a0002c0006t0001g0173 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.194-894G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81258782 | ||||||
| chr16:81258937
|
A | AAG | 4 | a0001c0001t0001g0001a0001c0001t0001g0178a0001c0001t0001g0182others(1): Show | 6 | NA18949.hp1 NA18988.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-724_194-723dup others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 81258937 | |||||
| chr16:81259002
|
G | T | 3 | a0001c0005t0001g0012a0001c0005t0001g0013a0006c0016t0001g0010 | 3 | HG02559.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.194-674G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259002 | ||||||
| chr16:81259019
|
C | G | 5 | a0001c0001t0001g0341a0001c0001t0001g0342a0003c0003t0001g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-657C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259019 | ||||||
| chr16:81259054
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.194-622C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259054 | ||||||
| chr16:81259125
|
C | G | 72 | a0001c0001t0001g0203a0001c0001t0001g0326a0001c0002t0001g0015others(69): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.194-551C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259125 | ||||||
| chr16:81259143
|
A | C | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | NA18944.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.194-533A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259143 | ||||||
| chr16:81259218
|
G | C | 1 | a0003c0003t0001g0367 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.194-458G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259218 | ||||||
| chr16:81259245
|
G | A | 8 | a0001c0002t0001g0015a0001c0005t0001g0027a0001c0005t0001g0151others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-431G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259245 | ||||||
| chr16:81259351
|
G | T | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.194-325G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259351 | ||||||
| chr16:81259355
|
G | A | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(3): Show | 6 | HG02280.hp2 HG02647.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-321G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259355 | ||||||
| chr16:81259363
|
G | A | 1 | a0003c0003t0001g0323 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.194-313G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259363 | ||||||
| chr16:81259438
|
G | A | 1 | a0003c0003t0001g0324 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.194-238G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259438 | ||||||
| chr16:81259457
|
A | G | 8 | a0001c0002t0001g0015a0001c0005t0001g0027a0001c0005t0001g0151others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-219A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259457 | ||||||
| chr16:81259493
|
A | T | 3 | a0001c0005t0001g0153a0001c0005t0001g0156a0010c0015t0001g0154 | 3 | HG02615.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.194-183A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259493 | ||||||
| chr16:81259516
|
A | G | 1 | a0002c0006t0001g0186 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.194-160A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259516 | ||||||
| chr16:81259579
|
A | T | 1 | a0002c0004t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.194-97A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259579 | ||||||
| chr16:81259602
|
A | G | 8 | a0001c0002t0001g0015a0001c0005t0001g0027a0001c0005t0001g0151others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-74A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259602 | ||||||
| chr16:81259630
|
C | T | 2 | a0001c0001t0001g0232a0001c0002t0001g0037 | 2 | NA18968.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.194-46C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259630 | ||||||
| chr16:81259655
|
A | T | 1 | a0001c0005t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.194-21A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 2/10 | chr16 | 81259655 | ||||||
| chr16:81260064
|
G | A | 7 | a0001c0002t0001g0015a0001c0005t0001g0027a0001c0005t0001g0151others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.323+259G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260064 | ||||||
| chr16:81260119
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.323+314A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260119 | ||||||
| chr16:81260196
|
C | G | 103 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(100): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.323+391C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260196 | ||||||
| chr16:81260225
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.323+420C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260225 | ||||||
| chr16:81260308
|
G | GA | 11 | a0001c0001t0001g0225a0001c0001t0001g0229a0001c0001t0001g0234others(8): Show | 11 | HG01255.hp2 HG01981.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.323+518dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81260308 | |||||
| chr16:81260308
|
GA | G | 46 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0213others(43): Show | 49 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.323+518delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81260308 | |||||
| chr16:81260387
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.323+582A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260387 | ||||||
| chr16:81260401
|
G | C | 2 | a0001c0001t0001g0361a0001c0001t0001g0362 | 2 | HG00621.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.323+596G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260401 | ||||||
| chr16:81260485
|
T | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(9): Show | 13 | HG01081.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+680T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260485 | ||||||
| chr16:81260518
|
A | G | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+713A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260518 | ||||||
| chr16:81260659
|
C | G | 2 | a0001c0001t0001g0347a0001c0001t0001g0374 | 2 | NA19074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.323+854C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260659 | ||||||
| chr16:81260715
|
A | C | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.323+910A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260715 | ||||||
| chr16:81260764
|
A | C | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.323+959A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260764 | ||||||
| chr16:81260837
|
A | C | 2 | a0001c0005t0001g0097a0006c0014t0001g0098 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.323+1032A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260837 | ||||||
| chr16:81260839
|
T | G | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.323+1034T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81260839 | ||||||
| chr16:81261114
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0225a0001c0001t0002g0204 | 4 | HG01071.hp2 HG02004.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-1022G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261114 | ||||||
| chr16:81261216
|
T | C | 4 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-920T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261216 | ||||||
| chr16:81261232
|
G | A | 2 | a0001c0001t0001g0164a0001c0002t0001g0149 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.324-904G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261232 | ||||||
| chr16:81261282
|
A | G | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.324-854A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261282 | ||||||
| chr16:81261284
|
T | G | 1 | a0001c0002t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324-852T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261284 | ||||||
| chr16:81261288
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(247): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.324-848T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261288 | ||||||
| chr16:81261403
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-733T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261403 | ||||||
| chr16:81261408
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-728T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261408 | ||||||
| chr16:81261409
|
C | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-727C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261409 | ||||||
| chr16:81261412
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-724G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261412 | ||||||
| chr16:81261415
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-721T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261415 | ||||||
| chr16:81261416
|
A | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-720A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261416 | ||||||
| chr16:81261453
|
A | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-683A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261453 | ||||||
| chr16:81261507
|
C | T | 1 | a0002c0004t0001g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.324-629C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261507 | ||||||
| chr16:81261523
|
T | C | 1 | a0002c0020t0001g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.324-613T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261523 | ||||||
| chr16:81261527
|
G | A | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324-609G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261527 | ||||||
| chr16:81261554
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-582T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261554 | ||||||
| chr16:81261581
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-555T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261581 | ||||||
| chr16:81261582
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-554T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261582 | ||||||
| chr16:81261584
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-552G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261584 | ||||||
| chr16:81261586
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-550G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261586 | ||||||
| chr16:81261587
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-549G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261587 | ||||||
| chr16:81261589
|
G | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-547G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261589 | ||||||
| chr16:81261594
|
G | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-542G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261594 | ||||||
| chr16:81261597
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-539G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261597 | ||||||
| chr16:81261598
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-538G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261598 | ||||||
| chr16:81261600
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-536T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261600 | ||||||
| chr16:81261603
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-533G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261603 | ||||||
| chr16:81261604
|
C | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-532C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261604 | ||||||
| chr16:81261614
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-522T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261614 | ||||||
| chr16:81261650
|
C | T | 1 | a0001c0002t0001g0042 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.324-486C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261650 | ||||||
| chr16:81261652
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-484T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261652 | ||||||
| chr16:81261653
|
G | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-483G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261653 | ||||||
| chr16:81261654
|
G | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-482G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261654 | ||||||
| chr16:81261659
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-477G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261659 | ||||||
| chr16:81261660
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-476T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261660 | ||||||
| chr16:81261661
|
C | T | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.324-475C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261661 | ||||||
| chr16:81261662
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-474T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261662 | ||||||
| chr16:81261663
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-473T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261663 | ||||||
| chr16:81261665
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-471G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261665 | ||||||
| chr16:81261668
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-468G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261668 | ||||||
| chr16:81261670
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-466G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261670 | ||||||
| chr16:81261674
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-462G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261674 | ||||||
| chr16:81261686
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-450T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261686 | ||||||
| chr16:81261696
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-440G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261696 | ||||||
| chr16:81261706
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-430G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261706 | ||||||
| chr16:81261709
|
C | A | 1 | a0002c0020t0001g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.324-427C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261709 | ||||||
| chr16:81261714
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-422T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261714 | ||||||
| chr16:81261715
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-421G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261715 | ||||||
| chr16:81261716
|
C | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-420C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261716 | ||||||
| chr16:81261723
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-413T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261723 | ||||||
| chr16:81261742
|
C | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-394C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261742 | ||||||
| chr16:81261743
|
A | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-393A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261743 | ||||||
| chr16:81261783
|
C | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-353C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261783 | ||||||
| chr16:81261785
|
A | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-351A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261785 | ||||||
| chr16:81261790
|
G | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-346G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261790 | ||||||
| chr16:81261791
|
G | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-345G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261791 | ||||||
| chr16:81261792
|
A | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-344A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261792 | ||||||
| chr16:81261795
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-341G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261795 | ||||||
| chr16:81261797
|
A | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-339A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261797 | ||||||
| chr16:81261799
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-337T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261799 | ||||||
| chr16:81261800
|
G | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-336G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261800 | ||||||
| chr16:81261801
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-335G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261801 | ||||||
| chr16:81261838
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-298T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261838 | ||||||
| chr16:81261845
|
C | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-291C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261845 | ||||||
| chr16:81261846
|
A | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-290A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261846 | ||||||
| chr16:81261848
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-288T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261848 | ||||||
| chr16:81261854
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-282G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261854 | ||||||
| chr16:81261863
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-273T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261863 | ||||||
| chr16:81261883
|
A | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-253A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261883 | ||||||
| chr16:81261884
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-252G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261884 | ||||||
| chr16:81261893
|
C | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-243C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261893 | ||||||
| chr16:81261902
|
CGGCTGAT others(25): Show |
C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-231_324-200del others(32): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81261902 | |||||
| chr16:81261938
|
T | C | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-198T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261938 | ||||||
| chr16:81261942
|
C | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-194C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261942 | ||||||
| chr16:81261946
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-190G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261946 | ||||||
| chr16:81261949
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-187G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261949 | ||||||
| chr16:81261965
|
A | T | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-171A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261965 | ||||||
| chr16:81261975
|
C | A | 1 | a0001c0002t0001g0166 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.324-161C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81261975 | ||||||
| chr16:81262032
|
A | G | 1 | a0001c0005t0001g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.324-104A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 3/10 | chr16 | 81262032 | ||||||
| chr16:81262297
|
T | C | 99 | a0001c0001t0001g0255a0001c0001t0001g0282a0001c0002t0001g0003others(96): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.471+14T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262297 | ||||||
| chr16:81262423
|
C | T | 2 | a0003c0003t0001g0335a0003c0003t0001g0338 | 2 | HG02040.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.471+140C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262423 | ||||||
| chr16:81262434
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.471+151C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262434 | ||||||
| chr16:81262633
|
GC | G | 10 | a0001c0002t0001g0135a0001c0005t0001g0114a0001c0005t0001g0116others(7): Show | 10 | HG00639.hp2 HG01433.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+352delC | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81262633 | |||||
| chr16:81262742
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.471+459G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262742 | ||||||
| chr16:81262780
|
T | C | 3 | a0001c0005t0001g0027a0001c0005t0001g0151a0001c0007t0001g0201 | 3 | HG02280.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.471+497T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262780 | ||||||
| chr16:81262836
|
C | A | 1 | a0001c0007t0001g0235 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.471+553C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262836 | ||||||
| chr16:81262836
|
CAAAA | C | 8 | a0001c0002t0001g0149a0001c0005t0001g0027a0001c0005t0001g0091others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.471+570_471+573del others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81262836 | |||||
| chr16:81262841
|
A | AAC | 94 | a0001c0001t0001g0255a0001c0001t0001g0282a0001c0002t0001g0003others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.471+559_471+560ins others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81262841 | |||||
| chr16:81262841
|
A | AC | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(162): Show | 169 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.471+558_471+559ins others(1): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262841 | ||||||
| chr16:81262841
|
A | ACAAAAAC | 7 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0269others(4): Show | 7 | HG01081.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+558_471+559ins others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262841 | ||||||
| chr16:81262842
|
A | C | 46 | a0001c0001t0001g0008a0001c0001t0001g0159a0001c0001t0001g0240others(43): Show | 49 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.471+559A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262842 | ||||||
| chr16:81262843
|
A | C | 1 | a0001c0001t0001g0317 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.471+560A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262843 | ||||||
| chr16:81262845
|
A | C | 9 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0002t0001g0169others(6): Show | 9 | HG00280.hp2 HG01074.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.471+562A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262845 | ||||||
| chr16:81262846
|
A | C | 8 | a0001c0002t0001g0149a0001c0005t0001g0027a0001c0005t0001g0091others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.471+563A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262846 | ||||||
| chr16:81262870
|
T | TA | 12 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0002t0001g0149others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.471+594dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81262870 | |||||
| chr16:81262935
|
C | A | 1 | a0002c0004t0001g0134 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.471+652C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262935 | ||||||
| chr16:81262998
|
C | T | 7 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0259others(4): Show | 7 | HG00673.hp1 HG02080.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+715C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81262998 | ||||||
| chr16:81263012
|
C | T | 1 | a0002c0020t0001g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.471+729C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263012 | ||||||
| chr16:81263094
|
T | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+811T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263094 | ||||||
| chr16:81263108
|
C | CT | 22 | a0001c0001t0001g0198a0001c0001t0001g0259a0001c0001t0001g0266others(19): Show | 22 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.471+845dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81263108 | |||||
| chr16:81263108
|
C | CTTTT | 7 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(4): Show | 7 | HG02055.hp2 HG02965.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+842_471+845dup others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81263108 | |||||
| chr16:81263108
|
CT | C | 7 | a0001c0001t0001g0269a0001c0001t0001g0342a0001c0002t0001g0036others(4): Show | 7 | HG00280.hp2 HG01081.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+845delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81263108 | |||||
| chr16:81263108
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.471+836_471+845del others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 81263108 | |||||
| chr16:81263162
|
G | C | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | NA18944.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.471+879G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263162 | ||||||
| chr16:81263188
|
G | A | 1 | a0002c0006t0001g0245 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.471+905G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263188 | ||||||
| chr16:81263196
|
C | T | 6 | a0001c0002t0001g0014a0001c0005t0001g0012a0001c0005t0001g0013others(3): Show | 6 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+913C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263196 | ||||||
| chr16:81263197
|
G | A | 1 | a0001c0005t0001g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.471+914G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263197 | ||||||
| chr16:81263259
|
T | G | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.471+976T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263259 | ||||||
| chr16:81263279
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.471+996T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263279 | ||||||
| chr16:81263301
|
G | A | 1 | a0001c0005t0001g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.471+1018G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263301 | ||||||
| chr16:81263311
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.471+1028C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263311 | ||||||
| chr16:81263385
|
C | A | 1 | a0001c0002t0001g0089 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.471+1102C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263385 | ||||||
| chr16:81263393
|
G | A | 1 | a0001c0002t0001g0073 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.471+1110G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263393 | ||||||
| chr16:81263441
|
G | C | 1 | a0001c0001t0001g0289 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.471+1158G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263441 | ||||||
| chr16:81263534
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0007t0001g0162others(1): Show | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-1106A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263534 | ||||||
| chr16:81263785
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0212 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.472-855A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263785 | ||||||
| chr16:81263837
|
C | T | 4 | a0001c0001t0001g0203a0003c0003t0001g0251a0003c0003t0001g0346others(1): Show | 4 | HG01261.hp2 HG01943.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-803C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263837 | ||||||
| chr16:81263876
|
T | A | 1 | a0001c0001t0001g0205 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.472-764T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263876 | ||||||
| chr16:81263902
|
C | T | 1 | a0001c0002t0001g0086 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.472-738C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263902 | ||||||
| chr16:81263909
|
G | C | 1 | a0001c0002t0001g0042 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.472-731G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263909 | ||||||
| chr16:81263971
|
A | C | 1 | a0002c0004t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.472-669A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81263971 | ||||||
| chr16:81264085
|
C | G | 1 | a0001c0002t0001g0089 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.472-555C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264085 | ||||||
| chr16:81264091
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0147others(156): Show | 162 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.472-549G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264091 | ||||||
| chr16:81264097
|
A | G | 79 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0326others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.472-543A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264097 | ||||||
| chr16:81264205
|
C | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0003c0003t0001g0313others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-435C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264205 | ||||||
| chr16:81264270
|
G | T | 5 | a0003c0003t0001g0334a0003c0003t0001g0335a0003c0003t0001g0336others(2): Show | 5 | HG02015.hp2 HG02040.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-370G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264270 | ||||||
| chr16:81264390
|
C | T | 2 | a0002c0004t0001g0035a0002c0004t0001g0106 | 2 | NA18968.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.472-250C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264390 | ||||||
| chr16:81264428
|
A | G | 43 | a0001c0001t0001g0326a0002c0004t0001g0032a0002c0004t0001g0033others(40): Show | 43 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.472-212A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264428 | ||||||
| chr16:81264472
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.472-168G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264472 | ||||||
| chr16:81264531
|
C | T | 1 | a0001c0002t0001g0067 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.472-109C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 4/10 | chr16 | 81264531 | ||||||
| chr16:81264860
|
G | A | 1 | a0001c0002t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.619+73G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81264860 | ||||||
| chr16:81264932
|
C | G | 9 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0197others(6): Show | 9 | HG00735.hp2 HG01106.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.619+145C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81264932 | ||||||
| chr16:81264983
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.619+196C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81264983 | ||||||
| chr16:81265034
|
A | G | 3 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0001t0001g0298 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.619+247A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265034 | ||||||
| chr16:81265046
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.619+259C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265046 | ||||||
| chr16:81265142
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.619+355A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265142 | ||||||
| chr16:81265177
|
C | G | 1 | a0002c0004t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.619+390C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265177 | ||||||
| chr16:81265204
|
TCACCCAT others(12): Show |
T | 1 | a0001c0005t0001g0126 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.619+430_619+448del others(19): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 81265204 | |||||
| chr16:81265213
|
C | T | 1 | a0001c0005t0001g0031 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.619+426C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265213 | ||||||
| chr16:81265221
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.619+434G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265221 | ||||||
| chr16:81265469
|
A | G | 9 | a0001c0005t0001g0012a0001c0005t0001g0013a0001c0005t0001g0027others(6): Show | 9 | HG02280.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.619+682A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265469 | ||||||
| chr16:81265475
|
C | T | 1 | a0001c0002t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.619+688C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265475 | ||||||
| chr16:81265482
|
C | T | 52 | a0001c0002t0001g0003a0001c0002t0001g0135a0001c0002t0001g0359others(49): Show | 53 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.619+695C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265482 | ||||||
| chr16:81265514
|
C | G | 1 | a0001c0007t0001g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.619+727C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265514 | ||||||
| chr16:81265564
|
T | A | 1 | a0002c0004t0001g0039 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.619+777T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265564 | ||||||
| chr16:81265574
|
T | A | 73 | a0001c0002t0001g0003a0001c0002t0001g0135a0001c0002t0001g0359others(70): Show | 75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.619+787T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265574 | ||||||
| chr16:81265676
|
G | A | 1 | a0001c0001t0001g0330 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.619+889G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265676 | ||||||
| chr16:81265676
|
G | C | 9 | a0001c0005t0001g0012a0001c0005t0001g0013a0001c0005t0001g0027others(6): Show | 9 | HG02280.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.619+889G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265676 | ||||||
| chr16:81265740
|
C | A | 1 | a0001c0005t0001g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.619+953C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265740 | ||||||
| chr16:81265758
|
G | C | 71 | a0001c0002t0001g0003a0001c0002t0001g0135a0001c0002t0001g0359others(68): Show | 73 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.619+971G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265758 | ||||||
| chr16:81265782
|
TCCACCAT others(51): Show |
T | 61 | a0001c0002t0001g0003a0001c0002t0001g0135a0001c0002t0001g0359others(58): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.619+1004_619+1061d others(60): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 81265782 | |||||
| chr16:81265844
|
C | T | 6 | a0001c0001t0001g0008a0001c0002t0001g0083a0001c0002t0001g0107others(3): Show | 7 | HG00738.hp2 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.619+1057C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265844 | ||||||
| chr16:81265887
|
C | T | 1 | a0001c0005t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.619+1100C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265887 | ||||||
| chr16:81265895
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.619+1108C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265895 | ||||||
| chr16:81265948
|
C | A | 6 | a0001c0001t0001g0242a0001c0001t0001g0264a0001c0001t0001g0273others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.619+1161C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81265948 | ||||||
| chr16:81266034
|
T | C | 3 | a0002c0004t0001g0090a0002c0004t0001g0103a0002c0004t0001g0104 | 3 | HG01167.hp2 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.619+1247T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266034 | ||||||
| chr16:81266079
|
A | G | 1 | a0001c0001t0001g0326 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.619+1292A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266079 | ||||||
| chr16:81266081
|
A | C | 49 | a0001c0002t0001g0003a0001c0002t0001g0135a0001c0002t0001g0359others(46): Show | 50 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.619+1294A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266081 | ||||||
| chr16:81266113
|
C | T | 1 | a0001c0005t0001g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.619+1326C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266113 | ||||||
| chr16:81266186
|
C | T | 39 | a0001c0002t0001g0003a0001c0002t0001g0135a0001c0002t0001g0359others(36): Show | 40 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.619+1399C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266186 | ||||||
| chr16:81266191
|
C | T | 39 | a0001c0002t0001g0003a0001c0002t0001g0135a0001c0002t0001g0359others(36): Show | 40 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.619+1404C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266191 | ||||||
| chr16:81266397
|
A | G | 1 | a0002c0004t0001g0139 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.620-1511A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266397 | ||||||
| chr16:81266619
|
C | G | 3 | a0001c0001t0001g0161a0002c0006t0001g0163a0002c0020t0001g0275 | 3 | HG03041.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.620-1289C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266619 | ||||||
| chr16:81266788
|
G | T | 38 | a0001c0002t0001g0003a0001c0002t0001g0135a0001c0002t0001g0359others(35): Show | 39 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.620-1120G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266788 | ||||||
| chr16:81266820
|
C | T | 1 | a0002c0006t0001g0245 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.620-1088C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266820 | ||||||
| chr16:81266886
|
C | G | 39 | a0001c0002t0001g0003a0001c0002t0001g0135a0001c0002t0001g0359others(36): Show | 40 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.620-1022C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266886 | ||||||
| chr16:81266995
|
G | A | 2 | a0001c0001t0001g0271a0001c0002t0001g0123 | 2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.620-913G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81266995 | ||||||
| chr16:81267026
|
C | T | 47 | a0001c0002t0001g0003a0001c0002t0001g0359a0001c0005t0001g0012others(44): Show | 48 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.620-882C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267026 | ||||||
| chr16:81267029
|
G | A | 5 | a0001c0005t0001g0012a0001c0005t0001g0013a0002c0004t0001g0009others(2): Show | 5 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.620-879G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267029 | ||||||
| chr16:81267159
|
G | A | 1 | a0002c0006t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.620-749G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267159 | ||||||
| chr16:81267293
|
C | T | 1 | a0001c0002t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.620-615C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267293 | ||||||
| chr16:81267348
|
C | T | 3 | a0002c0004t0001g0009a0002c0004t0001g0011a0002c0020t0001g0275 | 3 | HG02896.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.620-560C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267348 | ||||||
| chr16:81267411
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0344 | 3 | HG03704.hp2 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.620-497G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267411 | ||||||
| chr16:81267568
|
G | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0191a0001c0001t0001g0205others(6): Show | 10 | HG01071.hp2 HG02004.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.620-340G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267568 | ||||||
| chr16:81267622
|
G | T | 4 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0283others(1): Show | 4 | HG03688.hp2 HG03704.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-286G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267622 | ||||||
| chr16:81267671
|
G | A | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.620-237G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267671 | ||||||
| chr16:81267805
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.620-103G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267805 | ||||||
| chr16:81267810
|
T | C | 1 | a0002c0006t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.620-98T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267810 | ||||||
| chr16:81267855
|
G | C | 109 | a0001c0001t0001g0159a0001c0001t0001g0224a0001c0001t0001g0255others(106): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.620-53G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 5/10 | chr16 | 81267855 | ||||||
| chr16:81268222
|
TGGCATGG others(4): Show |
T | 47 | a0001c0005t0001g0012a0001c0005t0001g0013a0001c0005t0001g0020others(44): Show | 47 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.843+94_843+104delC others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81268222 | |||||
| chr16:81268326
|
C | T | 2 | a0001c0005t0001g0091a0002c0006t0001g0163 | 2 | HG02602.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.843+195C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268326 | ||||||
| chr16:81268358
|
C | T | 38 | a0001c0001t0001g0159a0001c0001t0001g0224a0001c0001t0001g0255others(35): Show | 39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.843+227C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268358 | ||||||
| chr16:81268404
|
A | G | 49 | a0001c0001t0001g0008a0001c0001t0001g0240a0001c0001t0001g0241others(46): Show | 52 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.843+273A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268404 | ||||||
| chr16:81268439
|
C | A | 1 | a0001c0007t0001g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843+308C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268439 | ||||||
| chr16:81268460
|
C | T | 1 | a0001c0005t0001g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.843+329C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268460 | ||||||
| chr16:81268486
|
C | T | 7 | a0001c0005t0001g0012a0001c0005t0001g0013a0001c0005t0001g0027others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+355C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268486 | ||||||
| chr16:81268524
|
C | CG | 3 | a0001c0002t0001g0076a0001c0005t0001g0143a0002c0004t0001g0035 | 3 | HG02109.hp1 NA18968.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.843+395dupG | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81268524 | |||||
| chr16:81268636
|
G | A | 2 | a0001c0001t0001g0385a0001c0001t0001g0386 | 2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.843+505G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268636 | ||||||
| chr16:81268650
|
T | C | 1 | a0001c0002t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+519T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268650 | ||||||
| chr16:81268679
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0157others(79): Show | 85 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.843+548A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268679 | ||||||
| chr16:81268737
|
A | T | 1 | a0003c0003t0001g0332 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.843+606A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268737 | ||||||
| chr16:81268739
|
G | A | 4 | a0001c0001t0001g0197a0001c0011t0001g0081a0001c0018t0001g0276others(1): Show | 4 | HG00735.hp2 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+608G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268739 | ||||||
| chr16:81268827
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.843+696G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81268827 | ||||||
| chr16:81269065
|
C | CT | 39 | a0001c0001t0001g0187a0001c0001t0001g0197a0001c0001t0001g0198others(36): Show | 39 | HG00735.hp2 HG01123.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.843+957dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | |||||
| chr16:81269065
|
C | CTTT | 28 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(25): Show | 28 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.843+955_843+957dup others(3): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | |||||
| chr16:81269065
|
C | CTTTT | 9 | a0001c0005t0001g0024a0001c0005t0001g0119a0001c0005t0001g0120others(6): Show | 9 | HG01258.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.843+954_843+957dup others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | |||||
| chr16:81269065
|
CT | C | 44 | a0001c0001t0001g0159a0001c0001t0001g0224a0001c0001t0001g0242others(41): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.843+957delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | |||||
| chr16:81269065
|
CTTT | C | 8 | a0002c0004t0001g0004a0002c0004t0001g0039a0002c0004t0001g0064others(5): Show | 9 | HG00140.hp1 HG01074.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+955_843+957del others(3): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | |||||
| chr16:81269065
|
CTTTT | C | 51 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0044others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.843+954_843+957del others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269065 | |||||
| chr16:81269070
|
T | A | 38 | a0001c0001t0001g0159a0001c0001t0001g0224a0001c0001t0001g0255others(35): Show | 39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.843+939T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269070 | ||||||
| chr16:81269074
|
T | A | 38 | a0001c0001t0001g0159a0001c0001t0001g0224a0001c0001t0001g0255others(35): Show | 39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.843+943T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269074 | ||||||
| chr16:81269167
|
C | G | 48 | a0001c0005t0001g0012a0001c0005t0001g0013a0001c0005t0001g0020others(45): Show | 48 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.844-992C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269167 | ||||||
| chr16:81269171
|
T | C | 39 | a0001c0001t0001g0159a0001c0001t0001g0224a0001c0001t0001g0255others(36): Show | 40 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.844-988T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269171 | ||||||
| chr16:81269301
|
C | CT | 52 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0192others(49): Show | 52 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.844-844dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269301 | |||||
| chr16:81269311
|
T | G | 1 | a0002c0006t0001g0311 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.844-848T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269311 | ||||||
| chr16:81269342
|
G | C | 7 | a0001c0005t0001g0012a0001c0005t0001g0013a0001c0005t0001g0027others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-817G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269342 | ||||||
| chr16:81269351
|
G | A | 48 | a0001c0001t0001g0008a0001c0001t0001g0240a0001c0001t0001g0241others(45): Show | 51 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.844-808G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269351 | ||||||
| chr16:81269434
|
T | C | 48 | a0001c0001t0001g0008a0001c0001t0001g0240a0001c0001t0001g0241others(45): Show | 51 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.844-725T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269434 | ||||||
| chr16:81269444
|
C | T | 3 | a0001c0005t0001g0091a0001c0007t0001g0235a0001c0007t0001g0392 | 3 | HG02602.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.844-715C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269444 | ||||||
| chr16:81269522
|
C | T | 37 | a0001c0005t0001g0020a0001c0005t0001g0021a0001c0005t0001g0022others(34): Show | 37 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.844-637C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269522 | ||||||
| chr16:81269534
|
C | G | 2 | a0002c0006t0001g0028a0002c0006t0001g0173 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.844-625C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269534 | ||||||
| chr16:81269719
|
C | T | 2 | a0002c0004t0001g0099a0002c0006t0001g0364 | 2 | NA18988.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.844-440C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269719 | ||||||
| chr16:81269758
|
T | C | 2 | a0002c0004t0001g0099a0002c0006t0001g0364 | 2 | NA18988.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.844-401T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81269758 | ||||||
| chr16:81269911
|
CAA | C | 3 | a0002c0004t0001g0009a0002c0004t0001g0011a0002c0020t0001g0275 | 3 | HG02896.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.844-246_844-245del others(2): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81269911 | |||||
| chr16:81270000
|
T | C | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.844-159T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81270000 | ||||||
| chr16:81270020
|
G | A | 38 | a0001c0001t0001g0159a0001c0001t0001g0255a0001c0001t0001g0259others(35): Show | 39 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.844-139G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81270020 | ||||||
| chr16:81270154
|
T | C | 67 | a0001c0001t0001g0211a0001c0001t0001g0318a0001c0002t0001g0127others(64): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
splice_region_variant&intron_variant | LOW | c.844-5T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 6/10 | chr16 | 81270154 | ||||||
| chr16:81270464
|
C | T | 80 | a0001c0001t0001g0255a0001c0001t0001g0259a0001c0001t0002g0204others(77): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1101+48C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270464 | ||||||
| chr16:81270535
|
A | G | 1 | a0003c0003t0001g0105 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1101+119A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270535 | ||||||
| chr16:81270586
|
T | TAGAAAAT others(321): Show |
1 | a0003c0003t0001g0324 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1101+186_1101+187i others(330): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270586 | |||||
| chr16:81270586
|
T | TAGAAAAT others(337): Show |
1 | a0003c0003t0001g0332 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1101+186_1101+187i others(346): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270586 | |||||
| chr16:81270682
|
C | CTTTCTGT others(1): Show |
5 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0260others(2): Show | 5 | HG01175.hp2 HG03017.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1101+267_1101+268i others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270682 | |||||
| chr16:81270686
|
C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0255a0001c0002t0001g0038a0001c0002t0001g0042others(4): Show | 7 | HG00423.hp1 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1101+275_1101+276i others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270686 | |||||
| chr16:81270686
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0001g0317 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1101+275_1101+276i others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270686 | |||||
| chr16:81270692
|
C | CTCTGTG | 6 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 7 | HG00597.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTCTGTGT others(1): Show |
58 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0159others(55): Show | 59 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTCTGTGT others(3): Show |
93 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0178others(90): Show | 95 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTCTGTGT others(5): Show |
13 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0262others(10): Show | 13 | HG00621.hp1 HG01081.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTCTGTGT others(7): Show |
4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0385others(1): Show | 4 | HG01106.hp2 HG01257.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+277_1101+278i others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTGTG | 43 | a0001c0001t0001g0273a0001c0005t0001g0012a0001c0005t0001g0013others(40): Show | 43 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1101+301_1101+304d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTGTGTG | 6 | a0001c0005t0001g0112a0001c0005t0001g0156a0002c0004t0001g0144others(3): Show | 6 | HG00558.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+299_1101+304d others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTGTGTGT others(1): Show |
41 | a0001c0001t0001g0259a0001c0001t0002g0204a0001c0002t0001g0003others(38): Show | 42 | HG00438.hp1 HG00609.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1101+297_1101+304d others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTGTGTGT others(3): Show |
31 | a0001c0001t0001g0318a0001c0002t0001g0015a0001c0002t0001g0056others(28): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1101+295_1101+304d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTGTGTGT others(5): Show |
26 | a0001c0001t0001g0008a0001c0002t0001g0067a0002c0004t0001g0032others(23): Show | 27 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1101+293_1101+304d others(14): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTGTGTGT others(7): Show |
36 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0325others(33): Show | 38 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1101+291_1101+304d others(16): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTGTGTGT others(9): Show |
7 | a0001c0002t0001g0083a0001c0002t0001g0107a0002c0004t0001g0103others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1101+289_1101+304d others(18): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | CTGTGTGT others(11): Show |
2 | a0001c0001t0001g0329a0009c0021t0001g0391 | 2 | HG04184.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1101+287_1101+304d others(20): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270692 | |||||
| chr16:81270692
|
C | G | 13 | a0001c0001t0001g0255a0001c0001t0001g0257a0001c0001t0001g0258others(10): Show | 13 | HG00423.hp1 HG01175.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1101+276C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270692 | ||||||
| chr16:81270703
|
T | G | 1 | a0001c0001t0001g0181 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1101+287T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270703 | ||||||
| chr16:81270749
|
AT | A | 74 | a0001c0001t0001g0255a0001c0001t0001g0259a0001c0001t0001g0277others(71): Show | 75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1101+346delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81270749 | |||||
| chr16:81270812
|
T | C | 1 | a0002c0006t0001g0245 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1101+396T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270812 | ||||||
| chr16:81270827
|
C | G | 1 | a0001c0007t0001g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1101+411C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81270827 | ||||||
| chr16:81271033
|
T | C | 9 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0269others(6): Show | 9 | HG01081.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101+617T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271033 | ||||||
| chr16:81271112
|
A | AT | 18 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 19 | HG01081.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1101+707dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81271112 | |||||
| chr16:81271115
|
T | TA | 45 | a0001c0001t0001g0008a0001c0001t0001g0240a0001c0001t0001g0241others(42): Show | 48 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1101+699_1101+700i others(3): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271115 | ||||||
| chr16:81271116
|
T | A | 6 | a0001c0002t0001g0015a0001c0007t0001g0235a0001c0007t0001g0392others(3): Show | 6 | HG00323.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1101+700T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271116 | ||||||
| chr16:81271116
|
T | TA | 160 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0147others(157): Show | 163 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.1101+700_1101+701i others(3): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271116 | ||||||
| chr16:81271117
|
T | A | 35 | a0001c0001t0001g0273a0001c0005t0001g0020a0001c0005t0001g0021others(32): Show | 35 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1101+701T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271117 | ||||||
| chr16:81271127
|
T | G | 1 | a0001c0002t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1101+711T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271127 | ||||||
| chr16:81271526
|
C | T | 3 | a0002c0004t0001g0092a0002c0004t0001g0128a0002c0004t0001g0139 | 3 | HG00099.hp1 HG01099.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1101+1110C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271526 | ||||||
| chr16:81271789
|
G | A | 1 | a0002c0006t0001g0312 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1101+1373G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271789 | ||||||
| chr16:81271804
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 10 | HG01106.hp2 HG01978.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1101+1388C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271804 | ||||||
| chr16:81271874
|
T | C | 10 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0269others(7): Show | 10 | HG01081.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1101+1458T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271874 | ||||||
| chr16:81271900
|
C | T | 301 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(298): Show | 308 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.1101+1484C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271900 | ||||||
| chr16:81271995
|
C | T | 1 | a0003c0003t0001g0301 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1101+1579C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271995 | ||||||
| chr16:81271996
|
C | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(124): Show | 132 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1101+1580C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271996 | ||||||
| chr16:81271999
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1101+1583C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81271999 | ||||||
| chr16:81272113
|
C | CT | 35 | a0001c0001t0001g0263a0001c0001t0001g0329a0001c0002t0001g0149others(32): Show | 35 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1101+1715dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272113 | |||||
| chr16:81272113
|
CT | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(233): Show | 243 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.1101+1715delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272113 | |||||
| chr16:81272144
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0308 | 2 | NA18940.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1101+1728C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272144 | ||||||
| chr16:81272226
|
T | G | 1 | a0001c0005t0001g0022 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1101+1810T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272226 | ||||||
| chr16:81272262
|
T | C | 2 | a0001c0001t0001g0350a0001c0002t0001g0015 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1101+1846T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272262 | ||||||
| chr16:81272293
|
AT | A | 4 | a0001c0001t0001g0366a0001c0001t0001g0379a0001c0001t0001g0380others(1): Show | 4 | HG01192.hp2 HG01361.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+1883delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272293 | |||||
| chr16:81272309
|
A | G | 41 | a0001c0001t0001g0318a0001c0001t0001g0356a0001c0002t0001g0016others(38): Show | 42 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1101+1893A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272309 | ||||||
| chr16:81272393
|
C | T | 4 | a0001c0001t0001g0164a0001c0005t0001g0012a0001c0005t0001g0013others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+1977C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272393 | ||||||
| chr16:81272441
|
T | C | 1 | a0001c0001t0001g0290 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1101+2025T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272441 | ||||||
| chr16:81272444
|
A | G | 5 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(2): Show | 5 | HG02027.hp1 NA18612.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1101+2028A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272444 | ||||||
| chr16:81272558
|
G | A | 383 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(380): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1101+2142G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272558 | ||||||
| chr16:81272566
|
G | A | 2 | a0001c0001t0001g0350a0001c0002t0001g0015 | 2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1101+2150G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272566 | ||||||
| chr16:81272659
|
A | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(279): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1101+2243A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272659 | ||||||
| chr16:81272730
|
A | T | 4 | a0001c0007t0001g0235a0001c0007t0001g0392a0002c0006t0001g0028others(1): Show | 4 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+2314A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272730 | ||||||
| chr16:81272742
|
C | T | 1 | a0002c0006t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1101+2326C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272742 | ||||||
| chr16:81272817
|
C | G | 2 | a0001c0005t0001g0091a0002c0004t0001g0134 | 2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1101+2401C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272817 | ||||||
| chr16:81272861
|
A | G | 3 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019 | 3 | HG00735.hp1 HG01070.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1101+2445A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272861 | ||||||
| chr16:81272882
|
G | A | 5 | a0003c0003t0001g0367a0003c0003t0001g0369a0003c0003t0001g0371others(2): Show | 5 | NA18947.hp2 NA18964.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1101+2466G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272882 | ||||||
| chr16:81272931
|
A | AGACTGGA others(31): Show |
1 | a0002c0004t0001g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1101+2516_1101+255 others(42): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272931 | |||||
| chr16:81272949
|
G | A | 316 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(313): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1101+2533G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272949 | ||||||
| chr16:81272965
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1101+2549C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272965 | ||||||
| chr16:81272967
|
A | T | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1101+2551A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81272967 | ||||||
| chr16:81272978
|
C | CT | 4 | a0001c0001t0001g0164a0001c0005t0001g0012a0001c0005t0001g0013others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+2567dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81272978 | |||||
| chr16:81273055
|
C | T | 1 | a0002c0006t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1101+2639C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273055 | ||||||
| chr16:81273116
|
T | C | 383 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(380): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1101+2700T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273116 | ||||||
| chr16:81273235
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(106): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1101+2819G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273235 | ||||||
| chr16:81273258
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(105): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.1101+2842C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273258 | ||||||
| chr16:81273278
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1101+2862C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273278 | ||||||
| chr16:81273279
|
G | A | 1 | a0002c0004t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1101+2863G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273279 | ||||||
| chr16:81273305
|
G | A | 53 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0382others(50): Show | 55 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1101+2889G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273305 | ||||||
| chr16:81273345
|
G | C | 54 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0382others(51): Show | 56 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1101+2929G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273345 | ||||||
| chr16:81273401
|
G | A | 1 | a0001c0005t0001g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1101+2985G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273401 | ||||||
| chr16:81273470
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG03017.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1101+3054C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273470 | ||||||
| chr16:81273533
|
G | C | 56 | a0001c0001t0001g0382a0001c0002t0001g0014a0001c0002t0001g0169others(53): Show | 58 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1101+3117G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273533 | ||||||
| chr16:81273561
|
C | T | 1 | a0001c0002t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1101+3145C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273561 | ||||||
| chr16:81273576
|
T | C | 2 | a0003c0003t0001g0313a0005c0010t0001g0343 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1101+3160T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273576 | ||||||
| chr16:81273582
|
G | A | 383 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(380): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1101+3166G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273582 | ||||||
| chr16:81273639
|
C | CT | 107 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(104): Show | 109 | HG00140.hp2 HG00280.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.1101+3235dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81273639 | |||||
| chr16:81273639
|
C | CTTT | 47 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(44): Show | 50 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1101+3233_1101+323 others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81273639 | |||||
| chr16:81273656
|
T | G | 1 | a0001c0002t0001g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1101+3240T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273656 | ||||||
| chr16:81273885
|
C | T | 2 | a0001c0002t0001g0071a0001c0002t0001g0072 | 2 | NA18944.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1101+3469C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273885 | ||||||
| chr16:81273966
|
G | A | 2 | a0003c0003t0001g0313a0005c0010t0001g0343 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1101+3550G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273966 | ||||||
| chr16:81273979
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(321): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1101+3563C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81273979 | ||||||
| chr16:81274011
|
G | C | 1 | a0001c0002t0001g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1101+3595G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274011 | ||||||
| chr16:81274099
|
A | G | 1 | a0001c0001t0002g0377 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1101+3683A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274099 | ||||||
| chr16:81274258
|
C | CT | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0308others(3): Show | 6 | HG00735.hp1 HG03225.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+3865dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81274258 | |||||
| chr16:81274258
|
CT | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1101+3865delT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81274258 | |||||
| chr16:81274258
|
CTT | C | 9 | a0001c0001t0001g0244a0001c0001t0001g0286a0001c0001t0001g0331others(6): Show | 9 | HG00323.hp2 HG01256.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101+3864_1101+386 others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81274258 | |||||
| chr16:81274357
|
G | A | 6 | a0001c0001t0001g0273a0001c0007t0001g0162a0002c0004t0001g0009others(3): Show | 6 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1101+3941G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274357 | ||||||
| chr16:81274373
|
G | C | 2 | a0003c0003t0001g0194a0003c0003t0001g0196 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1101+3957G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274373 | ||||||
| chr16:81274382
|
G | C | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1101+3966G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274382 | ||||||
| chr16:81274399
|
G | T | 2 | a0002c0004t0001g0009a0002c0004t0001g0011 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1101+3983G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274399 | ||||||
| chr16:81274486
|
G | A | 2 | a0001c0001t0001g0263a0001c0007t0001g0148 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1101+4070G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274486 | ||||||
| chr16:81274500
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1101+4084G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274500 | ||||||
| chr16:81274521
|
T | C | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1101+4105T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274521 | ||||||
| chr16:81274555
|
C | T | 1 | a0001c0005t0001g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1101+4139C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274555 | ||||||
| chr16:81274664
|
G | T | 6 | a0001c0001t0001g0164a0001c0005t0001g0012a0001c0005t0001g0013others(3): Show | 6 | HG02559.hp2 HG02602.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+4248G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274664 | ||||||
| chr16:81274747
|
C | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0270others(5): Show | 8 | HG00735.hp1 HG01070.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101+4331C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274747 | ||||||
| chr16:81274909
|
A | C | 4 | a0001c0001t0001g0164a0001c0005t0001g0012a0001c0005t0001g0013others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+4493A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274909 | ||||||
| chr16:81274913
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(220): Show | 227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1101+4497A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81274913 | ||||||
| chr16:81275014
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(76): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1101+4598T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275014 | ||||||
| chr16:81275081
|
C | T | 1 | a0001c0005t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1101+4665C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275081 | ||||||
| chr16:81275219
|
A | G | 1 | a0001c0001t0001g0331 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1101+4803A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275219 | ||||||
| chr16:81275244
|
C | T | 2 | a0001c0007t0001g0162a0008c0013t0001g0029 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1101+4828C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275244 | ||||||
| chr16:81275261
|
C | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(225): Show | 232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1101+4845C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275261 | ||||||
| chr16:81275508
|
A | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(229): Show | 236 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1101+5092A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275508 | ||||||
| chr16:81275758
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1102-5099T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275758 | ||||||
| chr16:81275859
|
G | A | 3 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0001t0001g0298 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1102-4998G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275859 | ||||||
| chr16:81275879
|
C | T | 34 | a0001c0001t0001g0193a0001c0001t0001g0208a0001c0001t0001g0223others(31): Show | 34 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.1102-4978C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275879 | ||||||
| chr16:81275884
|
T | A | 5 | a0001c0001t0001g0273a0001c0007t0001g0162a0002c0004t0001g0009others(2): Show | 5 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1102-4973T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275884 | ||||||
| chr16:81275979
|
C | A | 1 | a0001c0002t0001g0075 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1102-4878C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81275979 | ||||||
| chr16:81276021
|
G | A | 2 | a0001c0007t0001g0162a0008c0013t0001g0029 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-4836G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276021 | ||||||
| chr16:81276064
|
G | T | 1 | a0001c0001t0001g0207 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1102-4793G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276064 | ||||||
| chr16:81276065
|
G | T | 229 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(226): Show | 233 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1102-4792G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276065 | ||||||
| chr16:81276132
|
G | A | 288 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(285): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1102-4725G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276132 | ||||||
| chr16:81276161
|
G | A | 1 | a0002c0006t0001g0249 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1102-4696G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276161 | ||||||
| chr16:81276215
|
A | G | 1 | a0008c0013t0001g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1102-4642A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276215 | ||||||
| chr16:81276402
|
G | A | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(290): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1102-4455G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276402 | ||||||
| chr16:81276457
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0002t0001g0018others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102-4400C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276457 | ||||||
| chr16:81276700
|
G | A | 5 | a0001c0001t0001g0273a0001c0007t0001g0162a0002c0004t0001g0009others(2): Show | 5 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1102-4157G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276700 | ||||||
| chr16:81276926
|
G | T | 1 | a0001c0001t0001g0325 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1102-3931G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81276926 | ||||||
| chr16:81277002
|
G | A | 1 | a0001c0002t0001g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1102-3855G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277002 | ||||||
| chr16:81277060
|
G | A | 382 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(379): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1102-3797G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277060 | ||||||
| chr16:81277065
|
C | CA | 219 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(216): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1102-3773dupA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81277065 | |||||
| chr16:81277065
|
C | CAA | 10 | a0001c0001t0001g0195a0001c0001t0001g0211a0001c0001t0001g0221others(7): Show | 10 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.1102-3774_1102-377 others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81277065 | |||||
| chr16:81277097
|
A | T | 2 | a0001c0001t0001g0244a0001c0002t0001g0169 | 2 | HG02922.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1102-3760A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277097 | ||||||
| chr16:81277118
|
C | T | 1 | a0001c0007t0001g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1102-3739C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277118 | ||||||
| chr16:81277129
|
C | T | 1 | a0003c0003t0001g0105 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1102-3728C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277129 | ||||||
| chr16:81277158
|
G | A | 4 | a0001c0001t0001g0270a0001c0001t0001g0350a0001c0002t0001g0015others(1): Show | 4 | HG02895.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1102-3699G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277158 | ||||||
| chr16:81277165
|
T | G | 1 | a0001c0001t0001g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1102-3692T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277165 | ||||||
| chr16:81277197
|
T | C | 1 | a0001c0002t0001g0049 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1102-3660T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277197 | ||||||
| chr16:81277342
|
C | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(218): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1102-3515C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277342 | ||||||
| chr16:81277349
|
C | G | 1 | a0001c0001t0001g0393 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1102-3508C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277349 | ||||||
| chr16:81277420
|
C | T | 1 | a0002c0006t0001g0245 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1102-3437C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277420 | ||||||
| chr16:81277543
|
A | T | 1 | a0002c0006t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1102-3314A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277543 | ||||||
| chr16:81277610
|
G | A | 1 | a0001c0002t0001g0135 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1102-3247G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277610 | ||||||
| chr16:81277718
|
G | A | 1 | a0003c0003t0001g0291 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1102-3139G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277718 | ||||||
| chr16:81277728
|
T | C | 1 | a0002c0006t0001g0312 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1102-3129T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277728 | ||||||
| chr16:81277812
|
A | C | 1 | a0001c0005t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1102-3045A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277812 | ||||||
| chr16:81277880
|
G | C | 3 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0001t0001g0298 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1102-2977G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81277880 | ||||||
| chr16:81278073
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1102-2784G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278073 | ||||||
| chr16:81278091
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1102-2766G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278091 | ||||||
| chr16:81278103
|
G | A | 1 | a0001c0007t0001g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1102-2754G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278103 | ||||||
| chr16:81278127
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | NA18944.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1102-2730C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278127 | ||||||
| chr16:81278154
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0002t0001g0036others(8): Show | 13 | HG00597.hp1 HG00609.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102-2703G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278154 | ||||||
| chr16:81278232
|
G | A | 2 | a0003c0003t0001g0324a0003c0003t0001g0332 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1102-2625G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278232 | ||||||
| chr16:81278257
|
G | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0350a0001c0002t0001g0015 | 3 | HG02895.hp1 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1102-2600G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278257 | ||||||
| chr16:81278280
|
G | C | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1102-2577G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278280 | ||||||
| chr16:81278303
|
A | T | 1 | a0001c0005t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1102-2554A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278303 | ||||||
| chr16:81278425
|
C | A | 1 | a0003c0003t0001g0336 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1102-2432C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278425 | ||||||
| chr16:81278470
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1102-2387T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278470 | ||||||
| chr16:81278549
|
T | C | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1102-2308T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278549 | ||||||
| chr16:81278609
|
A | C | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1102-2248A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278609 | ||||||
| chr16:81278747
|
C | T | 2 | a0006c0014t0001g0098a0006c0016t0001g0010 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1102-2110C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278747 | ||||||
| chr16:81278954
|
A | G | 1 | a0001c0002t0001g0049 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1102-1903A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81278954 | ||||||
| chr16:81278967
|
G | GTTGGTTT others(58): Show |
1 | a0001c0005t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1102-1885_1102-182 others(69): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81278967 | |||||
| chr16:81279022
|
A | G | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1102-1835A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279022 | ||||||
| chr16:81279038
|
A | G | 1 | a0003c0003t0001g0360 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1102-1819A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279038 | ||||||
| chr16:81279145
|
C | T | 1 | a0003c0003t0001g0006 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1102-1712C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279145 | ||||||
| chr16:81279153
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1102-1704C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279153 | ||||||
| chr16:81279257
|
C | T | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1102-1600C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279257 | ||||||
| chr16:81279290
|
G | C | 1 | a0001c0005t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1102-1567G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279290 | ||||||
| chr16:81279297
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 7 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1102-1560T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279297 | ||||||
| chr16:81279344
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1102-1513C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279344 | ||||||
| chr16:81279361
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(85): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1102-1496A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279361 | ||||||
| chr16:81279397
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1102-1460C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279397 | ||||||
| chr16:81279401
|
G | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(84): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1102-1456G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279401 | ||||||
| chr16:81279411
|
G | A | 1 | a0003c0003t0001g0367 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1102-1446G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279411 | ||||||
| chr16:81279472
|
A | G | 1 | a0001c0001t0001g0331 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1102-1385A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279472 | ||||||
| chr16:81279832
|
A | G | 2 | a0002c0004t0001g0103a0002c0004t0001g0104 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1102-1025A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279832 | ||||||
| chr16:81279853
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0288 | 2 | NA18941.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1102-1004G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279853 | ||||||
| chr16:81279930
|
A | G | 2 | a0001c0001t0001g0366a0001c0001t0001g0381 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1102-927A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279930 | ||||||
| chr16:81279963
|
A | T | 215 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0147others(212): Show | 218 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1102-894A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81279963 | ||||||
| chr16:81280004
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(78): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1102-853T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280004 | ||||||
| chr16:81280138
|
C | A | 8 | a0001c0001t0001g0263a0001c0005t0001g0114a0001c0005t0001g0116others(5): Show | 8 | HG00639.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1102-719C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280138 | ||||||
| chr16:81280146
|
C | T | 58 | a0003c0003t0001g0006a0003c0003t0001g0007a0003c0003t0001g0105others(55): Show | 60 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1102-711C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280146 | ||||||
| chr16:81280148
|
A | C | 1 | a0001c0005t0001g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1102-709A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280148 | ||||||
| chr16:81280152
|
A | T | 1 | a0001c0001t0001g0234 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1102-705A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280152 | ||||||
| chr16:81280166
|
G | C | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1102-691G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280166 | ||||||
| chr16:81280269
|
CA | C | 6 | a0001c0001t0001g0297a0001c0002t0001g0018a0001c0002t0001g0019others(3): Show | 6 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1102-549delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAA | C | 11 | a0001c0001t0001g0280a0001c0001t0001g0393a0001c0002t0001g0014others(8): Show | 11 | HG00280.hp2 HG01358.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1102-550_1102-549d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAA | C | 26 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0261others(23): Show | 27 | HG00099.hp2 HG00597.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1102-551_1102-549d others(5): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAAA | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0257others(39): Show | 44 | HG00099.hp1 HG00609.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1102-552_1102-549d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAAAA | C | 42 | a0001c0001t0001g0329a0001c0005t0001g0023a0001c0005t0001g0024others(39): Show | 42 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1102-553_1102-549d others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAAAAA | C | 16 | a0001c0001t0001g0263a0001c0005t0001g0131a0001c0007t0001g0201others(13): Show | 18 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1102-554_1102-549d others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0001g0229a0001c0001t0001g0270a0001c0001t0001g0305others(7): Show | 10 | HG01109.hp1 HG01433.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1102-556_1102-549d others(10): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAAAAAA others(2): Show |
C | 54 | a0001c0001t0001g0157a0001c0001t0001g0164a0001c0001t0001g0182others(51): Show | 54 | HG00140.hp1 HG00423.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1102-557_1102-549d others(11): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAAAAAA others(3): Show |
C | 142 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0147others(139): Show | 145 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1102-558_1102-549d others(12): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAAAAAA others(4): Show |
C | 15 | a0001c0001t0001g0159a0001c0001t0001g0213a0001c0001t0001g0217others(12): Show | 15 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1102-559_1102-549d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAAAAAA others(10): Show |
C | 5 | a0001c0001t0001g0273a0001c0005t0001g0091a0002c0004t0001g0009others(2): Show | 5 | HG02602.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102-565_1102-549d others(19): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280269
|
CAAAAAAA others(15): Show |
C | 9 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(6): Show | 10 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1102-570_1102-549d others(24): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280269 | |||||
| chr16:81280292
|
A | T | 2 | a0001c0007t0001g0162a0008c0013t0001g0029 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-565A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280292 | ||||||
| chr16:81280293
|
A | T | 2 | a0001c0007t0001g0162a0008c0013t0001g0029 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-564A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280293 | ||||||
| chr16:81280295
|
A | C | 2 | a0001c0007t0001g0162a0008c0013t0001g0029 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-562A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280295 | ||||||
| chr16:81280297
|
A | C | 2 | a0001c0007t0001g0162a0008c0013t0001g0029 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-560A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280297 | ||||||
| chr16:81280298
|
AAAAAAAA others(4): Show |
A | 2 | a0001c0007t0001g0162a0008c0013t0001g0029 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-558_1102-548d others(13): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280298 | ||||||
| chr16:81280310
|
T | C | 2 | a0001c0007t0001g0162a0008c0013t0001g0029 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-547T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280310 | ||||||
| chr16:81280318
|
C | G | 59 | a0001c0007t0001g0162a0003c0003t0001g0006a0003c0003t0001g0007others(56): Show | 61 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1102-539C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280318 | ||||||
| chr16:81280320
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1102-537C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280320 | ||||||
| chr16:81280320
|
CACAG | C | 57 | a0003c0003t0001g0006a0003c0003t0001g0007a0003c0003t0001g0105others(54): Show | 59 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1102-533_1102-530d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280320 | |||||
| chr16:81280322
|
C | T | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1102-535C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280322 | ||||||
| chr16:81280324
|
G | C | 3 | a0001c0007t0001g0162a0003c0003t0001g0323a0008c0013t0001g0029 | 3 | HG02602.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1102-533G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280324 | ||||||
| chr16:81280324
|
G | GACAC | 5 | a0001c0001t0001g0273a0001c0005t0001g0091a0002c0004t0001g0009others(2): Show | 5 | HG02602.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102-509_1102-506d others(6): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280324 | |||||
| chr16:81280324
|
GAC | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1102-507_1102-506d others(4): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81280324 | |||||
| chr16:81280326
|
C | G | 1 | a0002c0022t0001g0333 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1102-531C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280326 | ||||||
| chr16:81280612
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1102-245A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280612 | ||||||
| chr16:81280680
|
C | T | 1 | a0001c0007t0001g0148 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1102-177C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280680 | ||||||
| chr16:81280776
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(74): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1102-81T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 7/10 | chr16 | 81280776 | ||||||
| chr16:81280973
|
T | C | 6 | a0001c0001t0001g0231a0001c0001t0001g0256a0001c0002t0001g0058others(3): Show | 6 | HG00408.hp2 HG02080.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207+11T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81280973 | ||||||
| chr16:81281174
|
G | A | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1207+212G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281174 | ||||||
| chr16:81281267
|
G | A | 7 | a0001c0001t0001g0273a0001c0005t0001g0091a0001c0007t0001g0162others(4): Show | 7 | HG02602.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1207+305G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281267 | ||||||
| chr16:81281280
|
T | C | 1 | a0003c0009t0001g0088 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1207+318T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281280 | ||||||
| chr16:81281314
|
C | T | 1 | a0003c0003t0001g0309 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1207+352C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281314 | ||||||
| chr16:81281407
|
T | C | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1207+445T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281407 | ||||||
| chr16:81281437
|
C | G | 1 | a0002c0006t0001g0150 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1207+475C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281437 | ||||||
| chr16:81281753
|
A | G | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1207+791A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281753 | ||||||
| chr16:81281795
|
C | G | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1207+833C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281795 | ||||||
| chr16:81281824
|
G | A | 1 | a0001c0001t0001g0355 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1207+862G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281824 | ||||||
| chr16:81281898
|
T | C | 2 | a0001c0001t0001g0318a0002c0006t0001g0238 | 2 | HG01928.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1207+936T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281898 | ||||||
| chr16:81281994
|
A | C | 1 | a0001c0001t0001g0286 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1207+1032A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81281994 | ||||||
| chr16:81282015
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1207+1053A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282015 | ||||||
| chr16:81282217
|
G | A | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1207+1255G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282217 | ||||||
| chr16:81282282
|
G | A | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1207+1320G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282282 | ||||||
| chr16:81282377
|
A | C | 1 | a0001c0001t0001g0355 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1207+1415A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282377 | ||||||
| chr16:81282482
|
T | G | 5 | a0001c0005t0001g0118a0001c0005t0001g0120a0001c0005t0001g0121others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+1520T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282482 | ||||||
| chr16:81282535
|
A | C | 1 | a0002c0004t0001g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1207+1573A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282535 | ||||||
| chr16:81282659
|
C | G | 358 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(355): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1207+1697C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282659 | ||||||
| chr16:81282710
|
T | G | 5 | a0001c0001t0001g0203a0002c0004t0001g0004a0002c0004t0001g0039others(2): Show | 6 | HG01257.hp1 HG01258.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207+1748T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282710 | ||||||
| chr16:81282717
|
A | G | 1 | a0003c0003t0001g0354 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1207+1755A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282717 | ||||||
| chr16:81282787
|
G | A | 210 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0147others(207): Show | 213 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1207+1825G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282787 | ||||||
| chr16:81282878
|
C | T | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1207+1916C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282878 | ||||||
| chr16:81282928
|
A | G | 60 | a0001c0001t0001g0203a0001c0001t0001g0393a0003c0003t0001g0006others(57): Show | 62 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1207+1966A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81282928 | ||||||
| chr16:81283320
|
T | G | 6 | a0001c0001t0001g0193a0001c0001t0001g0255a0001c0002t0001g0038others(3): Show | 6 | HG00423.hp1 HG01943.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-2220T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283320 | ||||||
| chr16:81283372
|
C | T | 1 | a0001c0002t0001g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1208-2168C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283372 | ||||||
| chr16:81283402
|
C | T | 1 | a0001c0001t0002g0372 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1208-2138C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283402 | ||||||
| chr16:81283583
|
C | T | 2 | a0001c0005t0001g0118a0002c0006t0001g0173 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1208-1957C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283583 | ||||||
| chr16:81283743
|
T | C | 1 | a0003c0003t0001g0292 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1208-1797T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283743 | ||||||
| chr16:81283793
|
GTTGGCGG others(4): Show |
G | 1 | a0001c0002t0001g0036 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1208-1746_1208-173 others(15): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283793 | ||||||
| chr16:81283959
|
G | A | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1208-1581G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283959 | ||||||
| chr16:81283967
|
T | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 7 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-1573T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81283967 | ||||||
| chr16:81284020
|
C | A | 2 | a0001c0005t0001g0122a0001c0005t0001g0132 | 2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1208-1520C>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284020 | ||||||
| chr16:81284125
|
G | A | 1 | a0001c0005t0001g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1208-1415G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284125 | ||||||
| chr16:81284228
|
A | T | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1208-1312A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284228 | ||||||
| chr16:81284240
|
TTATATAT others(37): Show |
T | 372 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(369): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1208-1283_1208-124 others(48): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284240 | |||||
| chr16:81284261
|
T | TTTATATA others(11): Show |
1 | a0002c0004t0001g0011 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1208-1279_1208-127 others(22): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284261 | ||||||
| chr16:81284261
|
TATATTTA others(15): Show |
T | 4 | a0001c0001t0001g0273a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-1274_1208-125 others(26): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284261 | |||||
| chr16:81284284
|
A | ATATT | 3 | a0001c0007t0001g0162a0002c0004t0001g0009a0002c0004t0001g0011 | 3 | HG02896.hp1 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1208-1253_1208-125 others(8): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284284 | |||||
| chr16:81284284
|
A | T | 4 | a0001c0001t0001g0273a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-1256A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284284 | ||||||
| chr16:81284548
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(81): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1208-992T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284548 | ||||||
| chr16:81284753
|
G | A | 1 | a0003c0003t0001g0324 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1208-787G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284753 | ||||||
| chr16:81284766
|
T | C | 1 | a0002c0004t0001g0130 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1208-774T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284766 | ||||||
| chr16:81284808
|
T | C | 1 | a0001c0001t0001g0287 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1208-732T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284808 | ||||||
| chr16:81284819
|
G | C | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1208-721G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284819 | ||||||
| chr16:81284819
|
G | GTTTTC | 2 | a0001c0001t0001g0001a0001c0001t0001g0184 | 4 | NA18988.hp2 NA18990.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-701_1208-697d others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284819 | |||||
| chr16:81284824
|
C | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 19 | HG00280.hp2 HG00733.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1208-716C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284824 | ||||||
| chr16:81284839
|
C | CT | 10 | a0001c0001t0001g0225a0001c0001t0001g0270a0001c0001t0001g0350others(7): Show | 10 | HG02630.hp1 HG02895.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1208-687dupT | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81284839 | |||||
| chr16:81284848
|
T | C | 4 | a0001c0001t0001g0164a0001c0005t0001g0012a0001c0005t0001g0013others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-692T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81284848 | ||||||
| chr16:81285039
|
C | T | 1 | a0001c0007t0001g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1208-501C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285039 | ||||||
| chr16:81285072
|
T | C | 1 | a0001c0001t0001g0366 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1208-468T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285072 | ||||||
| chr16:81285076
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | NA18944.hp1 NA18953.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1208-464G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285076 | ||||||
| chr16:81285146
|
C | T | 1 | a0001c0001t0001g0374 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1208-394C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285146 | ||||||
| chr16:81285154
|
C | T | 1 | a0001c0007t0001g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1208-386C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285154 | ||||||
| chr16:81285155
|
A | T | 1 | a0002c0006t0001g0150 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1208-385A>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285155 | ||||||
| chr16:81285160
|
A | G | 1 | a0002c0006t0001g0311 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1208-380A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285160 | ||||||
| chr16:81285170
|
A | G | 9 | a0001c0001t0001g0270a0001c0001t0001g0350a0001c0002t0001g0014others(6): Show | 9 | HG00735.hp1 HG01070.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1208-370A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285170 | ||||||
| chr16:81285276
|
G | C | 1 | a0001c0005t0001g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1208-264G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285276 | ||||||
| chr16:81285277
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0210others(76): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1208-263A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285277 | ||||||
| chr16:81285445
|
G | A | 1 | a0001c0005t0001g0121 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1208-95G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285445 | ||||||
| chr16:81285470
|
C | T | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1208-70C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285470 | ||||||
| chr16:81285496
|
C | T | 1 | a0001c0002t0001g0038 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1208-44C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 8/10 | chr16 | 81285496 | ||||||
| chr16:81285733
|
G | A | 5 | a0001c0001t0001g0273a0001c0007t0001g0162a0002c0004t0001g0009others(2): Show | 5 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+99G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285733 | ||||||
| chr16:81285814
|
A | C | 6 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(3): Show | 6 | HG00735.hp1 HG01070.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1302+180A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285814 | ||||||
| chr16:81285833
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0041others(94): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1302+199G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285833 | ||||||
| chr16:81285839
|
G | A | 1 | a0002c0020t0001g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1302+205G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285839 | ||||||
| chr16:81285878
|
A | C | 1 | a0003c0003t0001g0006 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1302+244A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81285878 | ||||||
| chr16:81286053
|
T | A | 8 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0018t0001g0276others(5): Show | 8 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+419T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286053 | ||||||
| chr16:81286053
|
TA | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0040others(89): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1302+429delA | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 81286053 | |||||
| chr16:81286194
|
C | T | 1 | a0002c0004t0001g0032 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1302+560C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286194 | ||||||
| chr16:81286314
|
T | A | 1 | a0001c0002t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1302+680T>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286314 | ||||||
| chr16:81286426
|
G | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 7 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1302+792G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286426 | ||||||
| chr16:81286476
|
G | A | 2 | a0006c0014t0001g0098a0006c0016t0001g0010 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1303-819G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286476 | ||||||
| chr16:81286515
|
A | C | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1303-780A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286515 | ||||||
| chr16:81286580
|
G | A | 1 | a0002c0004t0001g0134 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1303-715G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286580 | ||||||
| chr16:81286756
|
G | A | 1 | a0001c0007t0001g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1303-539G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286756 | ||||||
| chr16:81286802
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1303-493C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286802 | ||||||
| chr16:81286803
|
G | A | 2 | a0001c0001t0001g0374a0002c0004t0001g0129 | 2 | NA18945.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1303-492G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286803 | ||||||
| chr16:81286902
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1303-393C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286902 | ||||||
| chr16:81286907
|
C | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0210others(78): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1303-388C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81286907 | ||||||
| chr16:81287016
|
A | G | 1 | a0001c0001t0001g0344 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1303-279A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81287016 | ||||||
| chr16:81287224
|
C | T | 2 | a0003c0003t0001g0328a0003c0003t0001g0339 | 2 | HG00621.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1303-71C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81287224 | ||||||
| chr16:81287225
|
A | G | 383 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(380): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1303-70A>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81287225 | ||||||
| chr16:81287282
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 7 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-13G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 9/10 | chr16 | 81287282 | ||||||
| chr16:81287693
|
T | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0203others(81): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1414+287T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81287693 | ||||||
| chr16:81287918
|
T | G | 53 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0005t0001g0091others(50): Show | 55 | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1414+512T>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81287918 | ||||||
| chr16:81288055
|
C | T | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1414+649C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288055 | ||||||
| chr16:81288071
|
G | T | 1 | a0002c0004t0001g0139 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1414+665G>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288071 | ||||||
| chr16:81288099
|
G | A | 1 | a0001c0011t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1414+693G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288099 | ||||||
| chr16:81288101
|
G | A | 1 | a0001c0007t0001g0392 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1414+695G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288101 | ||||||
| chr16:81288173
|
G | A | 6 | a0001c0001t0001g0147a0001c0001t0001g0182a0001c0001t0001g0214others(3): Show | 6 | HG00438.hp2 HG00597.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1414+767G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288173 | ||||||
| chr16:81288204
|
C | T | 227 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0147others(224): Show | 230 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1414+798C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288204 | ||||||
| chr16:81288204
|
CATTAA | C | 44 | a0001c0005t0001g0091a0003c0003t0001g0006a0003c0003t0001g0007others(41): Show | 46 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1414+800_1414+804d others(7): Show |
BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 81288204 | |||||
| chr16:81288477
|
C | T | 1 | a0002c0004t0001g0134 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1414+1071C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288477 | ||||||
| chr16:81288503
|
G | A | 1 | a0002c0006t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1414+1097G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288503 | ||||||
| chr16:81288633
|
G | A | 3 | a0001c0001t0001g0273a0002c0004t0001g0009a0002c0004t0001g0011 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1414+1227G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288633 | ||||||
| chr16:81288715
|
A | C | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1414+1309A>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288715 | ||||||
| chr16:81288768
|
G | A | 4 | a0004c0008t0001g0054a0004c0008t0001g0084a0004c0008t0001g0096others(1): Show | 4 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414+1362G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288768 | ||||||
| chr16:81288838
|
G | C | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1414+1432G>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288838 | ||||||
| chr16:81288856
|
C | T | 1 | a0002c0004t0001g0134 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1414+1450C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81288856 | ||||||
| chr16:81289066
|
T | C | 383 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(380): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1415-1282T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289066 | ||||||
| chr16:81289184
|
C | T | 1 | a0002c0006t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1415-1164C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289184 | ||||||
| chr16:81289615
|
T | C | 1 | a0001c0005t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1415-733T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289615 | ||||||
| chr16:81289772
|
G | A | 1 | a0006c0014t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1415-576G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289772 | ||||||
| chr16:81289813
|
G | A | 1 | a0012c0012t0001g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1415-535G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289813 | ||||||
| chr16:81289901
|
G | A | 1 | a0001c0001t0002g0376 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1415-447G>A | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81289901 | ||||||
| chr16:81290015
|
C | G | 2 | a0001c0002t0001g0169a0001c0002t0001g0170 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1415-333C>G | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81290015 | ||||||
| chr16:81290148
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1415-200C>T | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81290148 | ||||||
| chr16:81290245
|
T | C | 2 | a0006c0014t0001g0098a0006c0016t0001g0010 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1415-103T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81290245 | ||||||
| chr16:81290316
|
T | C | 2 | a0006c0014t0001g0098a0006c0016t0001g0010 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1415-32T>C | BCO1 | ENSG00000135697.10 | transcript | ENST00000258168.7 | protein_coding | 10/10 | chr16 | 81290316 |