Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51411 |
|---|---|
| ensemblid | ENSG00000110934.13 |
| hgncid | 1053 |
| symbol | BIN2 |
| name | bridging integrator 2 |
| refseq_nuc | NM_016293.4 |
| refseq_prot | NP_057377.4 |
| ensembl_nuc | ENST00000615107.6 |
| ensembl_prot | ENSP00000483983.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 51281038 |
| end | 51324174 |
| strand | - |
| ver | v1.2 |
| region | chr12:51281038-51324174 |
| region5000 | chr12:51276038-51329174 |
| regionname0 | BIN2_chr12_51281038_51324174 |
| regionname5000 | BIN2_chr12_51276038_51329174 |
| 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 | 0/1 | 565 | 285 | 50 | 60 | 128 | 10 | 36 | 95 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002 | 0/0 | 565 | 40 | 7 | 3 | 30 | 0 | 0 | 25 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0003 | 1/0 | 565 | 32 | 26 | 1 | 0 | 0 | 4 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0004 | 0/0 | 565 | 31 | 8 | 3 | 16 | 2 | 2 | 12 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0005 | 0/0 | 565 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0006 | 0/0 | 565 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0007 | 0/0 | 43 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0008 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0009 | 0/0 | 565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0010 | 0/0 | 565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0011 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0012 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| 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 | 0/1 | 1698 | 250 | 46 | 56 | 104 | 10 | 33 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0002 | 0/0 | 1698 | 34 | 7 | 3 | 24 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0003 | 1/0 | 1698 | 32 | 26 | 1 | 0 | 0 | 4 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0004 | 0/0 | 1698 | 30 | 3 | 4 | 20 | 0 | 3 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0005 | 0/0 | 1698 | 23 | 8 | 3 | 8 | 2 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0006 | 0/0 | 1698 | 8 | 0 | 0 | 8 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0007 | 0/0 | 1698 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0008 | 0/0 | 1698 | 4 | 0 | 3 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0009 | 0/0 | 1698 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0010 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0011 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0012 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0013 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0014 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0015 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0016 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0017 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0018 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0019 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| c0020 | 0/0 | 1708 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| 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 | 534 | 315 | 77 | 55 | 133 | 10 | 38 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| t0002 | 0/0 | 534 | 67 | 14 | 13 | 40 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| t0003 | 0/0 | 534 | 11 | 0 | 4 | 0 | 2 | 5 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| t0004 | 0/0 | 534 | 3 | 0 | 0 | 3 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| t0005 | 0/0 | 534 | 2 | 1 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| t0006 | 0/0 | 534 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0004 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| 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 | 0/1 | 1698 | 250 | 46 | 56 | 104 | 10 | 33 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0004 | 0/0 | 1698 | 30 | 3 | 4 | 20 | 0 | 3 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0009 | 0/0 | 1698 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0019 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002c0002 | 0/0 | 1698 | 34 | 7 | 3 | 24 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002c0007 | 0/0 | 1698 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002c0011 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002c0012 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0003c0003 | 1/0 | 1698 | 32 | 26 | 1 | 0 | 0 | 4 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0004c0005 | 0/0 | 1698 | 23 | 8 | 3 | 8 | 2 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0004c0006 | 0/0 | 1698 | 8 | 0 | 0 | 8 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0005c0008 | 0/0 | 1698 | 4 | 0 | 3 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0006c0013 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0006c0014 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0007c0020 | 0/0 | 1708 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0008c0010 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0009c0017 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0010c0016 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0011c0015 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0012c0018 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2231 | 180 | 34 | 39 | 70 | 8 | 28 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0001t0002 | 0/0 | 2231 | 54 | 10 | 13 | 31 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0001t0003 | 0/0 | 2231 | 11 | 0 | 4 | 0 | 2 | 5 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0001t0004 | 0/0 | 2231 | 3 | 0 | 0 | 3 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0001t0006 | 0/0 | 2231 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0004t0001 | 0/0 | 2231 | 30 | 3 | 4 | 20 | 0 | 3 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0009t0002 | 0/0 | 2231 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0001c0019t0001 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002c0002t0001 | 0/0 | 2231 | 25 | 3 | 3 | 19 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002c0002t0002 | 0/0 | 2231 | 9 | 4 | 0 | 5 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002c0007t0001 | 0/0 | 2231 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002c0011t0001 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0002c0012t0001 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0003c0003t0001 | 1/0 | 2231 | 32 | 26 | 1 | 0 | 0 | 4 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0004c0005t0001 | 0/0 | 2231 | 22 | 7 | 3 | 8 | 2 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0004c0005t0005 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0004c0006t0001 | 0/0 | 2231 | 8 | 0 | 0 | 8 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0005c0008t0001 | 0/0 | 2231 | 3 | 0 | 3 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0005c0008t0005 | 0/0 | 2231 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0006c0013t0001 | 0/0 | 2231 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0006c0014t0001 | 0/0 | 2231 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0007c0020t0001 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0008c0010t0001 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0009c0017t0001 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0010c0016t0001 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0011c0015t0001 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| a0012c0018t0001 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | copy fasta | chr12 | 51276038 | 51329174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0006g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0009t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0009t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0009t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0009t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0019t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0007t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0007t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0007t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0011t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0012t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0005c0008t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0005c0008t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0005c0008t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0006c0013t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0006c0014t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0007c0020t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0008c0010t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0009c0017t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0010c0016t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0011c0015t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0012c0018t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00140 | hp2 | a0004 | c0005 | t0001 | g0040 | EUR | GBR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0085 | EUR | FIN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | FIN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00423 | hp1 | a0001 | c0009 | t0002 | g0171 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00438 | hp1 | a0004 | c0005 | t0001 | g0038 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00597 | hp2 | a0004 | c0005 | t0001 | g0037 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0306 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0332 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00642 | hp1 | a0006 | c0014 | t0001 | g0240 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00738 | hp1 | a0005 | c0008 | t0001 | g0257 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0290 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0364 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01106 | hp1 | a0004 | c0005 | t0001 | g0041 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0347 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01168 | hp2 | a0004 | c0005 | t0001 | g0050 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0359 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0348 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01256 | hp2 | a0005 | c0008 | t0001 | g0013 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01258 | hp1 | a0005 | c0008 | t0001 | g0013 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01261 | hp2 | a0006 | c0013 | t0001 | g0249 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0274 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01515 | hp2 | a0004 | c0005 | t0001 | g0051 | EUR | IBS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0122 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01891 | hp1 | a0001 | c0019 | t0001 | g0269 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0368 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02040 | hp2 | a0004 | c0005 | t0001 | g0033 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0355 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0081 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02056 | hp2 | a0004 | c0005 | t0001 | g0029 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0297 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0370 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02155 | hp1 | a0001 | c0009 | t0002 | g0174 | EAS | CDX | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02257 | hp2 | a0004 | c0005 | t0001 | g0036 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02280 | hp1 | a0004 | c0005 | t0001 | g0039 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0084 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0357 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0363 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0377 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0328 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0376 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0308 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02818 | hp1 | a0004 | c0005 | t0001 | g0047 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0302 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0295 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0296 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0303 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0373 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0319 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02970 | hp1 | a0008 | c0010 | t0001 | g0053 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02970 | hp2 | a0004 | c0005 | t0001 | g0049 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0225 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03130 | hp1 | a0004 | c0005 | t0001 | g0054 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0113 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03139 | hp2 | a0011 | c0015 | t0001 | g0152 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03209 | hp1 | a0004 | c0005 | t0005 | g0035 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0361 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0120 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03486 | hp2 | a0012 | c0018 | t0001 | g0114 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0374 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03491 | hp1 | a0001 | c0004 | t0001 | g0016 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0016 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0165 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03704 | hp1 | a0004 | c0005 | t0001 | g0026 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0349 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03831 | hp1 | a0004 | c0005 | t0001 | g0048 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0234 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03927 | hp1 | a0005 | c0008 | t0005 | g0252 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0164 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04184 | hp2 | a0003 | c0003 | t0001 | g0189 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0116 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04204 | hp2 | a0007 | c0020 | t0001 | g0375 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0352 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | CHB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0309 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18942 | hp1 | a0004 | c0006 | t0001 | g0023 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18943 | hp1 | a0004 | c0006 | t0001 | g0025 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18943 | hp2 | a0002 | c0011 | t0001 | g0073 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18946 | hp1 | a0001 | c0009 | t0002 | g0181 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18947 | hp2 | a0004 | c0006 | t0001 | g0042 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18948 | hp1 | a0001 | c0004 | t0001 | g0342 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18951 | hp2 | a0004 | c0006 | t0001 | g0030 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18953 | hp1 | a0002 | c0012 | t0001 | g0069 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18957 | hp2 | a0001 | c0004 | t0001 | g0341 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18961 | hp2 | a0001 | c0004 | t0001 | g0320 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0335 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18964 | hp1 | a0009 | c0017 | t0001 | g0366 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18966 | hp1 | a0004 | c0006 | t0001 | g0005 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18973 | hp1 | a0001 | c0004 | t0001 | g0261 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0311 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18978 | hp1 | a0001 | c0009 | t0002 | g0169 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18978 | hp2 | a0002 | c0007 | t0001 | g0062 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18979 | hp2 | a0004 | c0005 | t0001 | g0078 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18980 | hp2 | a0001 | c0004 | t0001 | g0327 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18988 | hp2 | a0002 | c0007 | t0001 | g0027 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18989 | hp2 | a0001 | c0004 | t0001 | g0299 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18990 | hp1 | a0001 | c0004 | t0001 | g0260 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18991 | hp1 | a0004 | c0006 | t0001 | g0005 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18992 | hp1 | a0004 | c0005 | t0001 | g0022 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0288 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18994 | hp1 | a0010 | c0016 | t0001 | g0094 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18994 | hp2 | a0004 | c0005 | t0001 | g0024 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18995 | hp2 | a0002 | c0007 | t0001 | g0031 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18997 | hp1 | a0001 | c0004 | t0001 | g0316 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19002 | hp1 | a0001 | c0004 | t0001 | g0360 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19011 | hp2 | a0002 | c0007 | t0001 | g0028 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19030 | hp1 | a0004 | c0005 | t0001 | g0052 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19030 | hp2 | a0004 | c0005 | t0001 | g0044 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19054 | hp1 | a0001 | c0004 | t0001 | g0292 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19063 | hp2 | a0004 | c0005 | t0001 | g0032 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19065 | hp2 | a0004 | c0006 | t0001 | g0045 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19066 | hp1 | a0001 | c0004 | t0001 | g0313 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0315 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0312 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19080 | hp1 | a0001 | c0004 | t0001 | g0310 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19088 | hp2 | a0001 | c0004 | t0001 | g0291 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19090 | hp1 | a0004 | c0006 | t0001 | g0043 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0346 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ASW | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0369 | AFR | ASW | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0307 | SAS | GIH | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01123 | hp1 | a0004 | c0005 | t0001 | g0046 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0305 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0233 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0371 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0153 | AFR | USA | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | USA | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | USA | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0104 | REF | REF | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0162 | REF | REF | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51288119
|
T | C | 8 | a0001a0002a0005others(5): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
missense_variant | MODERATE | c.1585A>G | p.Asn529Asp | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/13 | 1657/2231 | 1585/1698 | 529/565 | chr12 | 51288119 | ||
| chr12:51291775
|
G | A | 1 | a0011 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1331C>T | p.Ser444Leu | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1403/2231 | 1331/1698 | 444/565 | chr12 | 51291775 | ||
| chr12:51291897
|
C | A | 1 | a0008 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.1209G>T | p.Lys403Asn | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1281/2231 | 1209/1698 | 403/565 | chr12 | 51291897 | ||
| chr12:51291923
|
T | C | 1 | a0005 | 4 | HG00738.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
missense_variant | MODERATE | c.1183A>G | p.Ser395Gly | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1255/2231 | 1183/1698 | 395/565 | chr12 | 51291923 | ||
| chr12:51291932
|
G | A | 1 | a0010 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.1174C>T | p.Arg392Cys | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1246/2231 | 1174/1698 | 392/565 | chr12 | 51291932 | ||
| chr12:51299213
|
G | A | 1 | a0009 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.592C>T | p.Leu198Phe | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/13 | 664/2231 | 592/1698 | 198/565 | chr12 | 51299213 | ||
| chr12:51299237
|
C | T | 1 | a0006 | 2 | HG00642.hp1 HG01261.hp2 |
missense_variant | MODERATE | c.568G>A | p.Glu190Lys | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/13 | 640/2231 | 568/1698 | 190/565 | chr12 | 51299237 | ||
| chr12:51302694
|
T | C | 1 | a0012 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.304A>G | p.Ile102Val | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/13 | 376/2231 | 304/1698 | 102/565 | chr12 | 51302694 | ||
| chr12:51313842
|
C | T | 3 | a0002a0004a0008 | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
missense_variant | MODERATE | c.143G>A | p.Ser48Asn | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/13 | 215/2231 | 143/1698 | 48/565 | chr12 | 51313842 | ||
| chr12:51313889
|
C | CAATTTCT others(3): Show |
1 | a0007 | 1 | HG04204.hp2 | frameshift_variant | HIGH | c.86_95dupTGCAGAAATT | p.Leu32fs | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/13 | 167/2231 | 95/1698 | 32/565 | chr12 | 51313889 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51291927
|
G | A | 1 | a0002c0011 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.1179C>T | p.Thr393Thr | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1251/2231 | 1179/1698 | 393/565 | chr12 | 51291927 | ||
| chr12:51292047
|
T | C | 12 | a0001c0001a0001c0009a0001c0019others(9): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
synonymous_variant | LOW | c.1059A>G | p.Glu353Glu | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1131/2231 | 1059/1698 | 353/565 | chr12 | 51292047 | ||
| chr12:51292097
|
G | A | 1 | a0001c0009 | 4 | HG00423.hp1 HG02155.hp1 NA18946.hp1 others(1): Show |
synonymous_variant | LOW | c.1009C>T | p.Leu337Leu | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1081/2231 | 1009/1698 | 337/565 | chr12 | 51292097 | ||
| chr12:51299628
|
T | C | 1 | a0002c0012 | 1 | NA18953.hp1 | synonymous_variant | LOW | c.495A>G | p.Lys165Lys | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 6/13 | 567/2231 | 495/1698 | 165/565 | chr12 | 51299628 | ||
| chr12:51302089
|
G | A | 1 | a0004c0006 | 8 | NA18942.hp1 NA18943.hp1 NA18947.hp2 others(5): Show |
synonymous_variant | LOW | c.339C>T | p.Tyr113Tyr | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/13 | 411/2231 | 339/1698 | 113/565 | chr12 | 51302089 | ||
| chr12:51302716
|
G | A | 6 | a0002c0002a0002c0011a0002c0012others(3): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
synonymous_variant | LOW | c.282C>T | p.Asp94Asp | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/13 | 354/2231 | 282/1698 | 94/565 | chr12 | 51302716 | ||
| chr12:51313871
|
G | C | 1 | a0001c0019 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.114C>G | p.Thr38Thr | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/13 | 186/2231 | 114/1698 | 38/565 | chr12 | 51313871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51281082
|
C | T | 1 | a0001c0001t0003 | 11 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*417G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 417 | chr12 | 51281082 | |||||
| chr12:51281167
|
T | C | 1 | a0001c0001t0006 | 2 | HG02258.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*332A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 332 | chr12 | 51281167 | |||||
| chr12:51281177
|
T | C | 1 | a0001c0001t0004 | 3 | NA18939.hp2 NA18963.hp2 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*322A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 322 | chr12 | 51281177 | |||||
| chr12:51281424
|
C | T | 3 | a0001c0001t0002a0001c0009t0002a0002c0002t0002 | 67 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*75G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 75 | chr12 | 51281424 | |||||
| chr12:51281462
|
C | T | 2 | a0004c0005t0005a0005c0008t0005 | 2 | HG03209.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*37G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 37 | chr12 | 51281462 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51281660
|
A | G | 4 | a0004c0005t0001g0039a0004c0005t0001g0040a0004c0005t0001g0046others(1): Show | 4 | HG00140.hp2 HG01123.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-132T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51281660 | ||||||
| chr12:51281830
|
C | G | 1 | a0001c0001t0002g0215 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1669-302G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51281830 | ||||||
| chr12:51281886
|
G | T | 2 | a0001c0001t0001g0372a0001c0001t0001g0373 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1669-358C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51281886 | ||||||
| chr12:51281959
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1669-431A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51281959 | ||||||
| chr12:51282023
|
C | T | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1669-495G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282023 | ||||||
| chr12:51282119
|
T | A | 1 | a0001c0004t0001g0316 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-591A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282119 | ||||||
| chr12:51282264
|
A | T | 1 | a0002c0012t0001g0069 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1669-736T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282264 | ||||||
| chr12:51282266
|
C | CAT | 125 | a0001c0001t0001g0079a0001c0001t0001g0126a0001c0001t0001g0211others(122): Show | 135 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1669-740_1669-739d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282266 | ||||||
| chr12:51282266
|
C | CATAT | 186 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(183): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1669-742_1669-739d others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282266 | ||||||
| chr12:51282467
|
A | C | 1 | a0001c0004t0001g0316 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-939T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282467 | ||||||
| chr12:51282468
|
C | A | 1 | a0001c0004t0001g0316 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-940G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282468 | ||||||
| chr12:51282471
|
A | C | 1 | a0001c0004t0001g0316 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-943T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282471 | ||||||
| chr12:51282674
|
C | A | 7 | a0001c0001t0001g0236a0001c0001t0001g0250a0001c0001t0001g0258others(4): Show | 8 | HG00738.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1669-1146G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282674 | ||||||
| chr12:51282689
|
G | A | 294 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(291): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1669-1161C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282689 | ||||||
| chr12:51282751
|
G | A | 34 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(31): Show | 35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1669-1223C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282751 | ||||||
| chr12:51282838
|
A | G | 1 | a0008c0010t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1669-1310T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282838 | ||||||
| chr12:51282839
|
A | G | 20 | a0001c0001t0001g0126a0001c0001t0006g0270a0001c0001t0006g0361others(17): Show | 23 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.1669-1311T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282839 | ||||||
| chr12:51282916
|
A | T | 1 | a0001c0004t0001g0316 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-1388T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282916 | ||||||
| chr12:51283130
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1668+1586C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283130 | ||||||
| chr12:51283206
|
G | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 42 | HG00323.hp1 HG00558.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1668+1510C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283206 | ||||||
| chr12:51283234
|
A | T | 1 | a0001c0004t0001g0316 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1668+1482T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283234 | ||||||
| chr12:51283263
|
CA | C | 10 | a0003c0003t0001g0165a0003c0003t0001g0296a0003c0003t0001g0297others(7): Show | 10 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1668+1452delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283263 | ||||||
| chr12:51283263
|
CAA | C | 32 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(29): Show | 33 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1668+1451_1668+145 others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283263 | ||||||
| chr12:51283263
|
CAAAA | C | 271 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(268): Show | 289 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.1668+1449_1668+145 others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283263 | ||||||
| chr12:51283263
|
CAAAAA | C | 39 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(36): Show | 42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1668+1448_1668+145 others(9): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283263 | ||||||
| chr12:51283290
|
C | T | 3 | a0001c0001t0001g0224a0002c0002t0001g0060a0002c0002t0001g0061 | 3 | HG01109.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1668+1426G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283290 | ||||||
| chr12:51283304
|
A | C | 1 | a0001c0004t0001g0320 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1668+1412T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283304 | ||||||
| chr12:51283323
|
C | T | 2 | a0001c0001t0001g0017a0002c0002t0001g0059 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1668+1393G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283323 | ||||||
| chr12:51283349
|
G | A | 18 | a0001c0001t0001g0126a0002c0002t0001g0001a0002c0002t0001g0063others(15): Show | 21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1668+1367C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283349 | ||||||
| chr12:51283388
|
G | T | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1668+1328C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283388 | ||||||
| chr12:51283552
|
ATCC | A | 6 | a0001c0001t0002g0020a0001c0001t0002g0217a0001c0001t0002g0218others(3): Show | 6 | HG02451.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1668+1161_1668+116 others(7): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283552 | ||||||
| chr12:51283577
|
C | T | 1 | a0007c0020t0001g0375 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1668+1139G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283577 | ||||||
| chr12:51283717
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1668+999C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283717 | ||||||
| chr12:51283855
|
G | A | 1 | a0007c0020t0001g0375 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1668+861C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283855 | ||||||
| chr12:51283862
|
C | T | 1 | a0001c0001t0003g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1668+854G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283862 | ||||||
| chr12:51283933
|
C | T | 1 | a0003c0003t0001g0371 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1668+783G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283933 | ||||||
| chr12:51283941
|
C | T | 2 | a0004c0005t0001g0022a0008c0010t0001g0053 | 2 | HG02970.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1668+775G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283941 | ||||||
| chr12:51283942
|
G | A | 1 | a0002c0002t0001g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1668+774C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283942 | ||||||
| chr12:51283980
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1668+736A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283980 | ||||||
| chr12:51283993
|
C | CAA | 32 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0126others(29): Show | 35 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1668+721_1668+722d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283993 | ||||||
| chr12:51283993
|
C | CAAA | 274 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(271): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1668+720_1668+722d others(5): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283993 | ||||||
| chr12:51283993
|
C | CAAAA | 7 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 8 | HG01358.hp1 HG02071.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1668+719_1668+722d others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283993 | ||||||
| chr12:51283993
|
CA | C | 33 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(30): Show | 34 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1668+722delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283993 | ||||||
| chr12:51284007
|
A | T | 1 | a0004c0005t0001g0078 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1668+709T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51284007 | ||||||
| chr12:51284248
|
C | G | 3 | a0003c0003t0001g0165a0004c0005t0001g0052a0004c0005t0001g0054 | 3 | HG03130.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1668+468G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51284248 | ||||||
| chr12:51284550
|
C | T | 348 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(345): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1668+166G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51284550 | ||||||
| chr12:51284809
|
C | T | 1 | a0008c0010t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1597-22G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51284809 | ||||||
| chr12:51284820
|
G | T | 1 | a0008c0010t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1597-33C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51284820 | ||||||
| chr12:51285112
|
T | G | 1 | a0001c0001t0001g0258 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1597-325A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285112 | ||||||
| chr12:51285304
|
G | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1597-517C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285304 | ||||||
| chr12:51285463
|
T | A | 1 | a0006c0013t0001g0249 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1597-676A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285463 | ||||||
| chr12:51285470
|
T | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1597-683A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285470 | ||||||
| chr12:51285484
|
A | C | 13 | a0001c0001t0001g0285a0001c0001t0001g0317a0001c0001t0001g0318others(10): Show | 13 | HG00642.hp2 HG01261.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1597-697T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285484 | ||||||
| chr12:51285626
|
CT | C | 9 | a0001c0001t0002g0193a0003c0003t0001g0165a0003c0003t0001g0296others(6): Show | 9 | HG00558.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1597-840delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285626 | ||||||
| chr12:51285626
|
CTT | C | 251 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(248): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1597-841_1597-840d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285626 | ||||||
| chr12:51285817
|
A | G | 348 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(345): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1597-1030T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285817 | ||||||
| chr12:51285820
|
A | C | 348 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(345): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1597-1033T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285820 | ||||||
| chr12:51285843
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1597-1056G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285843 | ||||||
| chr12:51286002
|
C | T | 6 | a0003c0003t0001g0008a0003c0003t0001g0084a0003c0003t0001g0122others(3): Show | 7 | HG01346.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-1215G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286002 | ||||||
| chr12:51286026
|
G | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1597-1239C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286026 | ||||||
| chr12:51286080
|
G | A | 185 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1597-1293C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286080 | ||||||
| chr12:51286202
|
G | T | 1 | a0001c0001t0002g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1597-1415C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286202 | ||||||
| chr12:51286600
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1596+1508C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286600 | ||||||
| chr12:51286651
|
C | T | 34 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(31): Show | 35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1596+1457G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286651 | ||||||
| chr12:51287082
|
A | G | 18 | a0001c0001t0001g0126a0002c0002t0001g0001a0002c0002t0001g0063others(15): Show | 21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1596+1026T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287082 | ||||||
| chr12:51287098
|
A | G | 9 | a0001c0001t0001g0079a0001c0001t0001g0211a0001c0001t0001g0271others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+1010T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287098 | ||||||
| chr12:51287123
|
C | G | 2 | a0001c0001t0006g0270a0001c0001t0006g0361 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1596+985G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287123 | ||||||
| chr12:51287236
|
G | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1596+872C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287236 | ||||||
| chr12:51287240
|
A | T | 1 | a0001c0001t0001g0287 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1596+868T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287240 | ||||||
| chr12:51287338
|
G | GT | 47 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(44): Show | 48 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1596+769dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287338 | ||||||
| chr12:51287338
|
G | T | 1 | a0001c0004t0001g0341 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1596+770C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287338 | ||||||
| chr12:51287447
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1596+661G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287447 | ||||||
| chr12:51287572
|
C | G | 1 | a0001c0001t0001g0279 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1596+536G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287572 | ||||||
| chr12:51287593
|
G | A | 185 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1596+515C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287593 | ||||||
| chr12:51287623
|
A | G | 356 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(353): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1596+485T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287623 | ||||||
| chr12:51287649
|
G | GT | 53 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0137others(50): Show | 54 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1596+458dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287649 | ||||||
| chr12:51287745
|
G | A | 34 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(31): Show | 35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1596+363C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287745 | ||||||
| chr12:51287796
|
C | T | 20 | a0001c0001t0001g0126a0001c0001t0006g0270a0001c0001t0006g0361others(17): Show | 23 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596+312G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287796 | ||||||
| chr12:51287797
|
A | G | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1596+311T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287797 | ||||||
| chr12:51287837
|
G | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1596+271C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287837 | ||||||
| chr12:51287851
|
C | A | 2 | a0004c0005t0001g0052a0004c0005t0001g0054 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1596+257G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287851 | ||||||
| chr12:51288062
|
C | T | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1596+46G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51288062 | ||||||
| chr12:51288216
|
G | C | 1 | a0001c0001t0001g0322 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1516-28C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288216 | ||||||
| chr12:51288352
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1516-164G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288352 | ||||||
| chr12:51288375
|
G | A | 56 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(53): Show | 59 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1516-187C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288375 | ||||||
| chr12:51288382
|
C | A | 1 | a0001c0001t0001g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1516-194G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288382 | ||||||
| chr12:51288609
|
C | T | 6 | a0001c0004t0001g0311a0001c0004t0001g0327a0001c0004t0001g0332others(3): Show | 6 | HG00621.hp2 NA18948.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1516-421G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288609 | ||||||
| chr12:51288670
|
T | C | 1 | a0004c0006t0001g0042 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1516-482A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288670 | ||||||
| chr12:51288751
|
C | CT | 35 | a0003c0003t0001g0116a0003c0003t0001g0122a0003c0003t0001g0164others(32): Show | 36 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1516-564dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288751 | ||||||
| chr12:51288751
|
CT | C | 272 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(269): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1516-564delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288751 | ||||||
| chr12:51288875
|
G | A | 34 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(31): Show | 35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1516-687C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288875 | ||||||
| chr12:51288905
|
T | C | 3 | a0001c0001t0001g0224a0002c0002t0001g0060a0002c0002t0001g0061 | 3 | HG01109.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1516-717A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288905 | ||||||
| chr12:51288941
|
G | A | 34 | a0001c0004t0001g0016a0001c0004t0001g0260a0001c0004t0001g0261others(31): Show | 35 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1516-753C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288941 | ||||||
| chr12:51288969
|
C | T | 18 | a0001c0001t0001g0126a0002c0002t0001g0001a0002c0002t0001g0063others(15): Show | 21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1516-781G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288969 | ||||||
| chr12:51289040
|
G | C | 1 | a0001c0001t0001g0018 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1516-852C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289040 | ||||||
| chr12:51289069
|
A | C | 1 | a0001c0001t0001g0330 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1516-881T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289069 | ||||||
| chr12:51289088
|
G | C | 1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1516-900C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289088 | ||||||
| chr12:51289089
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1516-901G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289089 | ||||||
| chr12:51289111
|
G | T | 1 | a0002c0002t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1516-923C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289111 | ||||||
| chr12:51289155
|
C | T | 347 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(344): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1516-967G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289155 | ||||||
| chr12:51289206
|
T | A | 348 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(345): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1516-1018A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289206 | ||||||
| chr12:51289221
|
TA | T | 129 | a0001c0001t0001g0079a0001c0001t0001g0126a0001c0001t0001g0211others(126): Show | 139 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1516-1034delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289221 | ||||||
| chr12:51289221
|
TAAA | T | 185 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1516-1036_1516-103 others(7): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289221 | ||||||
| chr12:51289304
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1516-1116G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289304 | ||||||
| chr12:51289335
|
C | A | 2 | a0001c0001t0006g0270a0001c0001t0006g0361 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1516-1147G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289335 | ||||||
| chr12:51289723
|
A | T | 1 | a0001c0001t0002g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1516-1535T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289723 | ||||||
| chr12:51289922
|
C | G | 9 | a0001c0001t0001g0079a0001c0001t0001g0211a0001c0001t0001g0271others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1515+1669G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289922 | ||||||
| chr12:51290004
|
T | A | 18 | a0001c0001t0001g0126a0002c0002t0001g0001a0002c0002t0001g0063others(15): Show | 21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+1587A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290004 | ||||||
| chr12:51290040
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0129 | 2 | HG01433.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1515+1551G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290040 | ||||||
| chr12:51290191
|
C | T | 34 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(31): Show | 35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1515+1400G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290191 | ||||||
| chr12:51290202
|
G | A | 34 | a0001c0004t0001g0016a0001c0004t0001g0260a0001c0004t0001g0261others(31): Show | 35 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1515+1389C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290202 | ||||||
| chr12:51290231
|
T | C | 1 | a0001c0001t0002g0179 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1515+1360A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290231 | ||||||
| chr12:51290424
|
C | T | 8 | a0003c0003t0001g0165a0003c0003t0001g0296a0003c0003t0001g0297others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1515+1167G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290424 | ||||||
| chr12:51290705
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1515+886C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290705 | ||||||
| chr12:51290777
|
C | CA | 18 | a0001c0001t0001g0126a0002c0002t0001g0001a0002c0002t0001g0063others(15): Show | 21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+813dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290777 | ||||||
| chr12:51290809
|
C | T | 314 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(311): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1515+782G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290809 | ||||||
| chr12:51290849
|
T | C | 280 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(277): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1515+742A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290849 | ||||||
| chr12:51290919
|
C | T | 34 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(31): Show | 35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1515+672G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290919 | ||||||
| chr12:51290927
|
C | T | 1 | a0001c0001t0002g0201 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1515+664G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290927 | ||||||
| chr12:51290933
|
A | AAAAAC | 280 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(277): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1515+653_1515+657d others(7): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290933 | ||||||
| chr12:51291006
|
G | A | 34 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(31): Show | 35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1515+585C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291006 | ||||||
| chr12:51291040
|
T | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+551A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291040 | ||||||
| chr12:51291155
|
G | GCAAA | 7 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1515+432_1515+435d others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291155 | ||||||
| chr12:51291172
|
C | A | 2 | a0001c0001t0001g0344a0002c0002t0001g0034 | 2 | HG02027.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1515+419G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291172 | ||||||
| chr12:51291173
|
A | C | 8 | a0003c0003t0001g0165a0003c0003t0001g0296a0003c0003t0001g0297others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1515+418T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291173 | ||||||
| chr12:51291176
|
A | C | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1515+415T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291176 | ||||||
| chr12:51291512
|
CAGCCTGG others(1): Show |
C | 3 | a0003c0003t0001g0081a0003c0003t0001g0113a0003c0003t0001g0153 | 3 | HG02055.hp2 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1515+71_1515+78del others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291512 | ||||||
| chr12:51292420
|
T | C | 279 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.762-76A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292420 | ||||||
| chr12:51292501
|
A | T | 279 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.762-157T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292501 | ||||||
| chr12:51292590
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.762-246C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292590 | ||||||
| chr12:51292761
|
C | T | 261 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.762-417G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292761 | ||||||
| chr12:51292911
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.762-567C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292911 | ||||||
| chr12:51292928
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.762-584A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292928 | ||||||
| chr12:51293186
|
C | G | 2 | a0001c0001t0006g0270a0001c0001t0006g0361 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.762-842G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293186 | ||||||
| chr12:51293200
|
T | C | 279 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.762-856A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293200 | ||||||
| chr12:51293206
|
A | T | 18 | a0001c0001t0001g0126a0002c0002t0001g0001a0002c0002t0001g0063others(15): Show | 21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.762-862T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293206 | ||||||
| chr12:51293294
|
C | A | 311 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(308): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.762-950G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293294 | ||||||
| chr12:51293357
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0151 | 2 | NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.762-1013C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293357 | ||||||
| chr12:51293417
|
C | T | 1 | a0002c0002t0002g0067 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.762-1073G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293417 | ||||||
| chr12:51293454
|
C | T | 1 | a0001c0009t0002g0169 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.762-1110G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293454 | ||||||
| chr12:51293529
|
G | A | 7 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0242others(4): Show | 7 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.762-1185C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293529 | ||||||
| chr12:51293546
|
C | T | 261 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.762-1202G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293546 | ||||||
| chr12:51293599
|
A | G | 62 | a0001c0001t0001g0353a0001c0001t0002g0002a0001c0001t0002g0012others(59): Show | 68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.762-1255T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293599 | ||||||
| chr12:51293604
|
G | T | 1 | a0001c0001t0006g0361 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.762-1260C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293604 | ||||||
| chr12:51293655
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.762-1311G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293655 | ||||||
| chr12:51293739
|
G | A | 34 | a0001c0004t0001g0016a0001c0004t0001g0260a0001c0004t0001g0261others(31): Show | 35 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.762-1395C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293739 | ||||||
| chr12:51293780
|
A | T | 34 | a0003c0003t0001g0116a0003c0003t0001g0164a0003c0003t0001g0189others(31): Show | 35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.762-1436T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293780 | ||||||
| chr12:51293835
|
T | C | 7 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.762-1491A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293835 | ||||||
| chr12:51293926
|
C | A | 1 | a0010c0016t0001g0094 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.762-1582G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293926 | ||||||
| chr12:51293934
|
G | A | 279 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.762-1590C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293934 | ||||||
| chr12:51293957
|
C | T | 2 | a0001c0001t0001g0372a0001c0001t0001g0373 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.762-1613G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293957 | ||||||
| chr12:51294076
|
A | G | 279 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.761+1720T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294076 | ||||||
| chr12:51294136
|
TAAC | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0248a0001c0001t0001g0265 | 3 | HG01361.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.761+1657_761+1659d others(5): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294136 | ||||||
| chr12:51294196
|
T | A | 1 | a0001c0019t0001g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.761+1600A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294196 | ||||||
| chr12:51294207
|
A | G | 34 | a0001c0004t0001g0016a0001c0004t0001g0260a0001c0004t0001g0261others(31): Show | 35 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.761+1589T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294207 | ||||||
| chr12:51294264
|
T | C | 5 | a0001c0001t0001g0224a0001c0001t0006g0361a0002c0002t0001g0060others(2): Show | 5 | HG01109.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.761+1532A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294264 | ||||||
| chr12:51294296
|
T | G | 1 | a0001c0001t0001g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.761+1500A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294296 | ||||||
| chr12:51294322
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.761+1474T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294322 | ||||||
| chr12:51294394
|
G | A | 1 | a0001c0001t0006g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.761+1402C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294394 | ||||||
| chr12:51294401
|
T | C | 1 | a0008c0010t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.761+1395A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294401 | ||||||
| chr12:51294436
|
A | G | 1 | a0003c0003t0001g0153 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.761+1360T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294436 | ||||||
| chr12:51294460
|
T | G | 1 | a0001c0004t0001g0305 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.761+1336A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294460 | ||||||
| chr12:51294566
|
C | CA | 20 | a0001c0001t0001g0106a0001c0001t0001g0138a0001c0001t0001g0159others(17): Show | 20 | HG00597.hp1 HG01975.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.761+1229dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294566 | ||||||
| chr12:51294566
|
CA | C | 83 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0001g0271others(80): Show | 85 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+1229delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294566 | ||||||
| chr12:51294590
|
C | A | 42 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(39): Show | 43 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.761+1206G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294590 | ||||||
| chr12:51294658
|
GTTACATT others(5): Show |
G | 253 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(250): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.761+1126_761+1137d others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294658 | ||||||
| chr12:51294715
|
A | G | 1 | a0011c0015t0001g0152 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.761+1081T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294715 | ||||||
| chr12:51294723
|
GCACACAT others(7): Show |
G | 78 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 85 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+1059_761+1072d others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294723 | ||||||
| chr12:51294774
|
C | T | 19 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0195others(16): Show | 19 | HG00558.hp2 HG01978.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.761+1022G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294774 | ||||||
| chr12:51294912
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.761+884C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294912 | ||||||
| chr12:51294974
|
C | T | 31 | a0001c0001t0001g0349a0001c0004t0001g0016a0001c0004t0001g0260others(28): Show | 32 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.761+822G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294974 | ||||||
| chr12:51294999
|
C | T | 40 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(37): Show | 41 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.761+797G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294999 | ||||||
| chr12:51295202
|
C | T | 1 | a0001c0004t0001g0310 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.761+594G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295202 | ||||||
| chr12:51295234
|
C | A | 4 | a0001c0009t0002g0169a0001c0009t0002g0171a0001c0009t0002g0174others(1): Show | 4 | HG00423.hp1 HG02155.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.761+562G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295234 | ||||||
| chr12:51295235
|
AT | A | 113 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(110): Show | 118 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.761+560delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295235 | ||||||
| chr12:51295311
|
G | C | 83 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(80): Show | 87 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.761+485C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295311 | ||||||
| chr12:51295319
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.761+477G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295319 | ||||||
| chr12:51295392
|
C | CA | 25 | a0001c0001t0001g0087a0001c0001t0001g0145a0001c0001t0001g0304others(22): Show | 28 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.761+403dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295392 | ||||||
| chr12:51295392
|
CAAA | C | 49 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(46): Show | 52 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.761+401_761+403del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295392 | ||||||
| chr12:51295392
|
CAAAA | C | 113 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0191others(110): Show | 120 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.761+400_761+403del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295392 | ||||||
| chr12:51295392
|
CAAAAAA | C | 31 | a0001c0001t0001g0349a0001c0004t0001g0016a0001c0004t0001g0260others(28): Show | 32 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.761+398_761+403del others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295392 | ||||||
| chr12:51295432
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.761+364C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295432 | ||||||
| chr12:51295500
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.761+296A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295500 | ||||||
| chr12:51295571
|
AAAAAAAA others(39): Show |
A | 3 | a0001c0001t0001g0227a0001c0001t0003g0374a0001c0001t0004g0108 | 3 | HG03490.hp1 NA18954.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.761+179_761+224del others(46): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295571 | ||||||
| chr12:51295572
|
AAAAAAAT others(38): Show |
A | 2 | a0001c0001t0001g0104a0001c0001t0001g0154 | 2 | NA19089.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.761+179_761+223del others(45): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295572 | ||||||
| chr12:51295573
|
AAAAAATA others(39): Show |
A | 26 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 32 | HG00323.hp1 HG00558.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.761+177_761+222del others(46): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295573 | ||||||
| chr12:51295575
|
A | T | 1 | a0003c0003t0001g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.761+221T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295575 | ||||||
| chr12:51295575
|
AAAATATA others(17): Show |
A | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.761+197_761+220del others(24): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295575 | ||||||
| chr12:51295576
|
AAATATAT others(16): Show |
A | 1 | a0002c0002t0001g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.761+197_761+219del others(23): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | ||||||
| chr12:51295576
|
AAATATAT others(18): Show |
A | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.761+195_761+219del others(25): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | ||||||
| chr12:51295576
|
AAATATAT others(20): Show |
A | 2 | a0001c0001t0006g0270a0001c0019t0001g0269 | 2 | HG01891.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.761+193_761+219del others(27): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | ||||||
| chr12:51295576
|
AAATATAT others(22): Show |
A | 1 | a0003c0003t0001g0368 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.761+191_761+219del others(29): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | ||||||
| chr12:51295576
|
AAATATAT others(28): Show |
A | 1 | a0002c0002t0001g0072 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.761+185_761+219del others(35): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | ||||||
| chr12:51295577
|
A | T | 2 | a0001c0001t0001g0277a0003c0003t0001g0164 | 2 | HG02074.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.761+219T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AAT | A | 11 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(8): Show | 11 | HG00099.hp1 HG01928.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.761+217_761+218del others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATAT | A | 20 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0089others(17): Show | 21 | HG00140.hp1 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.761+215_761+218del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATAT | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0124a0001c0001t0001g0126others(14): Show | 18 | HG01257.hp1 HG01258.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.761+213_761+218del others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(1): Show |
A | 13 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(10): Show | 13 | HG01975.hp1 HG01993.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.761+211_761+218del others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(3): Show |
A | 10 | a0001c0001t0001g0137a0001c0001t0001g0279a0001c0001t0001g0294others(7): Show | 10 | HG01099.hp2 HG01243.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.761+209_761+218del others(10): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(5): Show |
A | 3 | a0001c0001t0001g0283a0003c0003t0001g0113a0003c0003t0001g0153 | 3 | HG00735.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.761+207_761+218del others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(7): Show |
A | 2 | a0001c0001t0001g0128a0010c0016t0001g0094 | 2 | NA18994.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.761+205_761+218del others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(15): Show |
A | 2 | a0001c0001t0001g0015a0005c0008t0005g0252 | 3 | HG03490.hp2 HG03492.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.761+197_761+218del others(22): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(17): Show |
A | 12 | a0001c0001t0001g0019a0001c0001t0001g0236a0001c0001t0001g0239others(9): Show | 13 | HG00738.hp1 HG01099.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.761+195_761+218del others(24): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(19): Show |
A | 15 | a0001c0001t0001g0018a0001c0001t0001g0349a0001c0004t0001g0016others(12): Show | 16 | HG00423.hp2 HG00609.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.761+193_761+218del others(26): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(21): Show |
A | 4 | a0001c0004t0001g0319a0001c0004t0001g0348a0001c0004t0001g0359others(1): Show | 4 | HG01192.hp1 HG01243.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.761+191_761+218del others(28): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(23): Show |
A | 3 | a0001c0001t0001g0017a0001c0001t0001g0367a0001c0001t0001g0376 | 4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.761+189_761+218del others(30): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(25): Show |
A | 1 | a0001c0001t0001g0331 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.761+187_761+218del others(32): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(27): Show |
A | 3 | a0001c0001t0002g0184a0001c0001t0002g0196a0001c0009t0002g0169 | 3 | HG01981.hp1 NA18978.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.761+185_761+218del others(34): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(29): Show |
A | 25 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0002g0222others(22): Show | 28 | HG00408.hp2 HG00609.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.761+183_761+218del others(36): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295577
|
AATATATA others(37): Show |
A | 32 | a0001c0001t0001g0273a0003c0003t0001g0189a0003c0003t0001g0234others(29): Show | 33 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.761+175_761+218del others(44): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | ||||||
| chr12:51295578
|
ATAT | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0150a0001c0001t0001g0304 | 3 | HG02071.hp2 NA19054.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.761+215_761+217del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295578
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0119a0001c0001t0001g0314 | 2 | HG00323.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.761+207_761+217del others(11): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295578
|
ATATATAT others(6): Show |
A | 3 | a0001c0001t0001g0211a0001c0001t0001g0301a0001c0001t0002g0210 | 3 | HG00733.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.761+205_761+217del others(13): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295578
|
ATATATAT others(10): Show |
A | 4 | a0001c0001t0001g0142a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | NA18953.hp2 NA18980.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.761+201_761+217del others(17): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295578
|
ATATATAT others(16): Show |
A | 3 | a0001c0001t0001g0243a0001c0001t0001g0254a0001c0001t0001g0266 | 3 | HG00639.hp1 HG01978.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.761+195_761+217del others(23): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295578
|
ATATATAT others(18): Show |
A | 25 | a0001c0001t0001g0014a0001c0001t0001g0235a0001c0001t0001g0238others(22): Show | 26 | HG00099.hp2 HG00642.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.761+193_761+217del others(25): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295578
|
ATATATAT others(20): Show |
A | 7 | a0001c0004t0001g0311a0001c0004t0001g0327a0001c0004t0001g0332others(4): Show | 7 | HG00621.hp2 HG02451.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.761+191_761+217del others(27): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295578
|
ATATATAT others(22): Show |
A | 6 | a0001c0001t0001g0372a0001c0001t0001g0373a0001c0004t0001g0347others(3): Show | 6 | HG01167.hp1 HG02145.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+189_761+217del others(29): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295578
|
ATATATAT others(28): Show |
A | 63 | a0001c0001t0001g0086a0001c0001t0001g0191a0001c0001t0001g0213others(60): Show | 68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.761+183_761+217del others(35): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295578
|
ATATATAT others(38): Show |
A | 9 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(6): Show | 9 | HG01346.hp1 HG01884.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.761+173_761+217del others(45): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | ||||||
| chr12:51295579
|
T | A | 9 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0135others(6): Show | 9 | HG01175.hp2 HG01261.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.761+217A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295579 | ||||||
| chr12:51295579
|
T | G | 8 | a0002c0002t0001g0055a0002c0002t0001g0059a0002c0002t0001g0060others(5): Show | 9 | HG01109.hp1 HG01167.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.761+217A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295579 | ||||||
| chr12:51295580
|
ATATATAT others(28): Show |
A | 8 | a0002c0002t0001g0055a0002c0002t0001g0059a0002c0002t0001g0060others(5): Show | 9 | HG01109.hp1 HG01167.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.761+181_761+215del others(35): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295580 | ||||||
| chr12:51295581
|
T | A | 15 | a0001c0001t0001g0087a0001c0001t0001g0133a0001c0001t0001g0135others(12): Show | 15 | HG00099.hp1 HG00642.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.761+215A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295581 | ||||||
| chr12:51295583
|
T | A | 24 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0089others(21): Show | 25 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.761+213A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295583 | ||||||
| chr12:51295585
|
T | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0080a0001c0001t0001g0087others(21): Show | 26 | HG00140.hp1 HG00639.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.761+211A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295585 | ||||||
| chr12:51295587
|
T | A | 23 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(20): Show | 23 | HG00140.hp1 HG00639.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.761+209A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295587 | ||||||
| chr12:51295589
|
T | A | 17 | a0001c0001t0001g0092a0001c0001t0001g0124a0001c0001t0001g0278others(14): Show | 17 | HG01099.hp2 HG01243.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.761+207A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295589 | ||||||
| chr12:51295591
|
T | A | 10 | a0001c0001t0001g0119a0001c0001t0001g0279a0001c0001t0001g0283others(7): Show | 10 | HG00323.hp2 HG00735.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.761+205A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295591 | ||||||
| chr12:51295593
|
T | A | 6 | a0001c0001t0001g0279a0001c0001t0001g0314a0003c0003t0001g0113others(3): Show | 6 | HG00323.hp2 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+203A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295593 | ||||||
| chr12:51295595
|
T | A | 3 | a0003c0003t0001g0113a0003c0003t0001g0153a0003c0003t0001g0225 | 3 | HG03041.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.761+201A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295595 | ||||||
| chr12:51295597
|
T | A | 1 | a0001c0001t0001g0148 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.761+199A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295597 | ||||||
| chr12:51295601
|
T | A | 2 | a0001c0001t0001g0015a0005c0008t0005g0252 | 3 | HG03490.hp2 HG03492.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.761+195A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295601 | ||||||
| chr12:51295603
|
T | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0246a0001c0001t0001g0253others(6): Show | 11 | HG00639.hp1 HG00738.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.761+193A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295603 | ||||||
| chr12:51295605
|
T | A | 39 | a0001c0001t0001g0014a0001c0001t0001g0235a0001c0001t0001g0238others(36): Show | 41 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.761+191A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295605 | ||||||
| chr12:51295607
|
T | A | 33 | a0001c0001t0001g0235a0001c0001t0001g0349a0001c0004t0001g0016others(30): Show | 34 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.761+189A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295607 | ||||||
| chr12:51295609
|
T | A | 39 | a0001c0001t0001g0017a0001c0001t0001g0349a0001c0001t0001g0367others(36): Show | 41 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.761+187A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295609 | ||||||
| chr12:51295611
|
T | A | 26 | a0001c0001t0001g0017a0001c0001t0001g0331a0001c0001t0001g0349others(23): Show | 27 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.761+185A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295611 | ||||||
| chr12:51295613
|
T | A | 11 | a0001c0001t0001g0331a0001c0001t0002g0184a0001c0001t0002g0196others(8): Show | 11 | HG01167.hp1 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.761+183A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295613 | ||||||
| chr12:51295613
|
T | G | 1 | a0002c0002t0001g0072 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.761+183A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295613 | ||||||
| chr12:51295614
|
A | G | 18 | a0002c0002t0001g0001a0002c0002t0001g0063a0002c0002t0001g0064others(15): Show | 21 | HG00408.hp2 HG00609.hp1 HG03130.hp1 others(18): Show |
intron_variant | MODIFIER | c.761+182T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295614 | ||||||
| chr12:51295615
|
T | A | 19 | a0002c0002t0001g0001a0002c0002t0001g0063a0002c0002t0001g0064others(16): Show | 22 | HG00408.hp2 HG00609.hp1 HG03130.hp1 others(19): Show |
intron_variant | MODIFIER | c.761+181A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295615 | ||||||
| chr12:51295615
|
T | G | 73 | a0001c0001t0001g0086a0001c0001t0001g0191a0001c0001t0001g0213others(70): Show | 78 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.761+181A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295615 | ||||||
| chr12:51295617
|
T | A | 100 | a0001c0001t0001g0086a0001c0001t0001g0191a0001c0001t0001g0213others(97): Show | 109 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.761+179A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295617 | ||||||
| chr12:51295619
|
T | A | 100 | a0001c0001t0001g0086a0001c0001t0001g0191a0001c0001t0001g0213others(97): Show | 109 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.761+177A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295619 | ||||||
| chr12:51295620
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.761+176T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295620 | ||||||
| chr12:51295621
|
T | A | 100 | a0001c0001t0001g0086a0001c0001t0001g0191a0001c0001t0001g0213others(97): Show | 109 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.761+175A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295621 | ||||||
| chr12:51295623
|
T | A | 132 | a0001c0001t0001g0086a0001c0001t0001g0191a0001c0001t0001g0213others(129): Show | 142 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.761+173A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295623 | ||||||
| chr12:51295625
|
T | G | 141 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0191others(138): Show | 151 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.761+171A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295625 | ||||||
| chr12:51295627
|
T | A | 141 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0191others(138): Show | 151 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.761+169A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295627 | ||||||
| chr12:51295890
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.679-12T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51295890 | ||||||
| chr12:51296177
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.679-299A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296177 | ||||||
| chr12:51296365
|
T | A | 1 | a0004c0005t0001g0040 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.679-487A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296365 | ||||||
| chr12:51296390
|
G | A | 17 | a0002c0002t0001g0001a0002c0002t0001g0063a0002c0002t0001g0064others(14): Show | 20 | HG00408.hp2 HG00609.hp1 NA18612.hp2 others(17): Show |
intron_variant | MODIFIER | c.679-512C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296390 | ||||||
| chr12:51296496
|
C | CA | 12 | a0001c0001t0001g0079a0001c0001t0001g0266a0001c0001t0001g0271others(9): Show | 12 | HG01346.hp1 HG01978.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.678+592dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296496 | ||||||
| chr12:51296496
|
CA | C | 31 | a0001c0001t0001g0151a0001c0001t0001g0349a0001c0004t0001g0016others(28): Show | 32 | HG00609.hp2 HG00621.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.678+592delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296496 | ||||||
| chr12:51296510
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.678+579G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296510 | ||||||
| chr12:51296518
|
C | A | 2 | a0001c0004t0001g0290a0001c0004t0001g0328 | 2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.678+571G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296518 | ||||||
| chr12:51296589
|
G | C | 1 | a0001c0001t0001g0339 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.678+500C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296589 | ||||||
| chr12:51296607
|
T | C | 9 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(6): Show | 10 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.678+482A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296607 | ||||||
| chr12:51296729
|
A | G | 1 | a0004c0005t0001g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.678+360T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296729 | ||||||
| chr12:51296737
|
G | C | 13 | a0002c0002t0001g0001a0002c0002t0001g0063a0002c0002t0001g0064others(10): Show | 16 | HG00408.hp2 HG00609.hp1 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.678+352C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296737 | ||||||
| chr12:51296967
|
G | T | 40 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(37): Show | 41 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.678+122C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296967 | ||||||
| chr12:51297053
|
A | C | 1 | a0001c0001t0001g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.678+36T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51297053 | ||||||
| chr12:51297064
|
C | T | 1 | a0004c0005t0001g0040 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.678+25G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51297064 | ||||||
| chr12:51297261
|
C | A | 1 | a0002c0002t0001g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.603-97G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297261 | ||||||
| chr12:51297343
|
C | T | 126 | a0001c0001t0001g0017a0001c0001t0001g0079a0001c0001t0001g0126others(123): Show | 129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.603-179G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297343 | ||||||
| chr12:51297353
|
A | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0228 | 3 | NA18954.hp2 NA18977.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.603-189T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297353 | ||||||
| chr12:51297364
|
C | G | 1 | a0001c0001t0001g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.603-200G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297364 | ||||||
| chr12:51297365
|
A | G | 149 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(146): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.603-201T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297365 | ||||||
| chr12:51297379
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.603-215A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297379 | ||||||
| chr12:51297403
|
T | TA | 141 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 149 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.603-240dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297403 | ||||||
| chr12:51297423
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.603-259G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297423 | ||||||
| chr12:51297441
|
C | T | 3 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0157 | 3 | NA18939.hp2 NA18963.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.603-277G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297441 | ||||||
| chr12:51297629
|
G | A | 255 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(252): Show | 274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.603-465C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297629 | ||||||
| chr12:51297767
|
A | G | 219 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(216): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.603-603T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297767 | ||||||
| chr12:51297826
|
C | T | 216 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(213): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.603-662G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297826 | ||||||
| chr12:51297838
|
G | GT | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.603-675dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297838 | ||||||
| chr12:51297851
|
C | T | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.603-687G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297851 | ||||||
| chr12:51297879
|
C | T | 1 | a0002c0002t0001g0072 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.603-715G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297879 | ||||||
| chr12:51298000
|
C | G | 7 | a0004c0006t0001g0005a0004c0006t0001g0023a0004c0006t0001g0025others(4): Show | 8 | NA18942.hp1 NA18943.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.603-836G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298000 | ||||||
| chr12:51298145
|
A | G | 213 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(210): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.603-981T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298145 | ||||||
| chr12:51298149
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.603-985C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298149 | ||||||
| chr12:51298168
|
T | C | 208 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(205): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.603-1004A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298168 | ||||||
| chr12:51298197
|
C | A | 1 | a0001c0001t0002g0197 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.602+1006G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298197 | ||||||
| chr12:51298320
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.602+883G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298320 | ||||||
| chr12:51298552
|
T | A | 208 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(205): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.602+651A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298552 | ||||||
| chr12:51298556
|
T | A | 21 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0063others(18): Show | 25 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.602+647A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298556 | ||||||
| chr12:51298641
|
A | C | 67 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(64): Show | 70 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.602+562T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298641 | ||||||
| chr12:51298795
|
A | G | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.602+408T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298795 | ||||||
| chr12:51298894
|
C | A | 1 | a0002c0011t0001g0073 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.602+309G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298894 | ||||||
| chr12:51298995
|
C | T | 1 | a0001c0004t0001g0316 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.602+208G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298995 | ||||||
| chr12:51299051
|
G | C | 2 | a0004c0005t0001g0052a0004c0005t0001g0054 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.602+152C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51299051 | ||||||
| chr12:51299092
|
G | C | 28 | a0004c0005t0001g0022a0004c0005t0001g0024a0004c0005t0001g0026others(25): Show | 29 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.602+111C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51299092 | ||||||
| chr12:51299093
|
GC | G | 165 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(162): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.602+109delG | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51299093 | ||||||
| chr12:51299094
|
C | G | 20 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(17): Show | 21 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.602+109G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51299094 | ||||||
| chr12:51299331
|
C | T | 6 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-43G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 6/12 | chr12 | 51299331 | ||||||
| chr12:51299573
|
G | A | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.516+34C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 6/12 | chr12 | 51299573 | ||||||
| chr12:51299831
|
C | T | 1 | a0001c0001t0001g0017 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.409-117G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51299831 | ||||||
| chr12:51299832
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.409-118C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51299832 | ||||||
| chr12:51299848
|
G | GT | 158 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(155): Show | 164 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.409-135dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51299848 | ||||||
| chr12:51300118
|
A | G | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.409-404T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300118 | ||||||
| chr12:51300119
|
G | T | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.409-405C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300119 | ||||||
| chr12:51300167
|
C | T | 1 | a0008c0010t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.409-453G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300167 | ||||||
| chr12:51300249
|
T | C | 32 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0055others(29): Show | 37 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.409-535A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300249 | ||||||
| chr12:51300372
|
G | A | 102 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(99): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.409-658C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300372 | ||||||
| chr12:51300494
|
C | T | 102 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(99): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.409-780G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300494 | ||||||
| chr12:51300625
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.409-911T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300625 | ||||||
| chr12:51300657
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.409-943C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300657 | ||||||
| chr12:51300737
|
C | A | 1 | a0002c0007t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.409-1023G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300737 | ||||||
| chr12:51300811
|
T | G | 28 | a0004c0005t0001g0022a0004c0005t0001g0024a0004c0005t0001g0026others(25): Show | 29 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.409-1097A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300811 | ||||||
| chr12:51300959
|
G | A | 2 | a0001c0001t0001g0362a0001c0001t0006g0361 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.408+1061C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300959 | ||||||
| chr12:51301150
|
G | A | 1 | a0003c0003t0001g0357 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.408+870C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301150 | ||||||
| chr12:51301183
|
A | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(5): Show | 8 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+837T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301183 | ||||||
| chr12:51301418
|
C | T | 1 | a0008c0010t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408+602G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301418 | ||||||
| chr12:51301446
|
A | G | 1 | a0001c0001t0001g0352 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.408+574T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301446 | ||||||
| chr12:51301500
|
C | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG01070.hp2 HG02735.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+520G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301500 | ||||||
| chr12:51301574
|
T | C | 1 | a0001c0004t0001g0360 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.408+446A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301574 | ||||||
| chr12:51301924
|
C | T | 58 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(55): Show | 64 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.408+96G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301924 | ||||||
| chr12:51302007
|
GT | G | 28 | a0004c0005t0001g0022a0004c0005t0001g0024a0004c0005t0001g0026others(25): Show | 29 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.408+12delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51302007 | ||||||
| chr12:51302145
|
G | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-30C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/12 | chr12 | 51302145 | ||||||
| chr12:51302163
|
A | C | 1 | a0003c0003t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.313-48T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/12 | chr12 | 51302163 | ||||||
| chr12:51302316
|
C | T | 1 | a0008c0010t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-201G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/12 | chr12 | 51302316 | ||||||
| chr12:51302638
|
C | T | 1 | a0001c0009t0002g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.312+48G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/12 | chr12 | 51302638 | ||||||
| chr12:51303302
|
G | A | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.163-161C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303302 | ||||||
| chr12:51303378
|
T | C | 62 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(59): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-237A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303378 | ||||||
| chr12:51303555
|
C | T | 1 | a0001c0004t0001g0359 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.163-414G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303555 | ||||||
| chr12:51303833
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.163-692G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303833 | ||||||
| chr12:51303906
|
T | C | 1 | a0001c0001t0006g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-765A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303906 | ||||||
| chr12:51303971
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163-830C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303971 | ||||||
| chr12:51304107
|
T | A | 40 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(37): Show | 43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.163-966A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304107 | ||||||
| chr12:51304159
|
C | T | 2 | a0004c0005t0001g0052a0004c0005t0001g0054 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.163-1018G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304159 | ||||||
| chr12:51304172
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-1031C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304172 | ||||||
| chr12:51304672
|
A | C | 164 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(161): Show | 172 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.163-1531T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304672 | ||||||
| chr12:51304714
|
A | C | 1 | a0001c0001t0001g0017 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.163-1573T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304714 | ||||||
| chr12:51304835
|
T | C | 1 | a0001c0001t0001g0015 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.163-1694A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304835 | ||||||
| chr12:51304982
|
T | C | 62 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(59): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-1841A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304982 | ||||||
| chr12:51304986
|
C | G | 102 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(99): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163-1845G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304986 | ||||||
| chr12:51305064
|
C | T | 6 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-1923G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305064 | ||||||
| chr12:51305121
|
G | A | 1 | a0001c0001t0006g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-1980C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305121 | ||||||
| chr12:51305250
|
C | T | 40 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(37): Show | 43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.163-2109G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305250 | ||||||
| chr12:51305309
|
T | A | 63 | a0001c0001t0002g0020a0002c0002t0001g0001a0002c0002t0001g0021others(60): Show | 69 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.163-2168A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305309 | ||||||
| chr12:51305445
|
G | A | 1 | a0003c0003t0001g0297 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2304C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305445 | ||||||
| chr12:51305523
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.163-2382G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305523 | ||||||
| chr12:51305573
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0002g0222 | 3 | HG02572.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.163-2432C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305573 | ||||||
| chr12:51305596
|
C | T | 1 | a0001c0001t0006g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2455G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305596 | ||||||
| chr12:51305605
|
C | G | 1 | a0001c0001t0002g0218 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.163-2464G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305605 | ||||||
| chr12:51305623
|
CA | C | 57 | a0001c0001t0001g0119a0002c0002t0001g0001a0002c0002t0001g0021others(54): Show | 63 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.163-2483delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305623 | ||||||
| chr12:51305716
|
ATTTAC | A | 3 | a0003c0003t0001g0296a0003c0003t0001g0303a0003c0003t0001g0309 | 3 | HG02895.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.163-2580_163-2576d others(7): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305716 | ||||||
| chr12:51305792
|
ATT | A | 67 | a0001c0001t0001g0159a0001c0001t0001g0191a0001c0001t0001g0211others(64): Show | 71 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-2653_163-2652d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305792 | ||||||
| chr12:51305826
|
C | CT | 64 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0100others(61): Show | 65 | HG00408.hp1 HG00621.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.163-2686dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305826 | ||||||
| chr12:51305826
|
C | CTT | 8 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0118others(5): Show | 8 | HG00140.hp1 HG00423.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2687_163-2686d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305826 | ||||||
| chr12:51305826
|
CT | C | 27 | a0001c0001t0002g0207a0001c0001t0002g0220a0001c0004t0001g0320others(24): Show | 31 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.163-2686delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305826 | ||||||
| chr12:51305826
|
CTTTT | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(35): Show | 41 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.163-2689_163-2686d others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305826 | ||||||
| chr12:51305829
|
T | TC | 3 | a0004c0005t0001g0036a0004c0005t0001g0046a0004c0006t0001g0042 | 3 | HG01123.hp1 HG02257.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.163-2689_163-2688i others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305829 | ||||||
| chr12:51305830
|
T | C | 37 | a0002c0002t0001g0034a0002c0002t0001g0055a0002c0002t0001g0056others(34): Show | 39 | HG00438.hp1 HG00597.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.163-2689A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305830 | ||||||
| chr12:51305831
|
T | C | 22 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0063others(19): Show | 26 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.163-2690A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305831 | ||||||
| chr12:51305832
|
T | C | 1 | a0001c0001t0001g0352 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.163-2691A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305832 | ||||||
| chr12:51305834
|
T | C | 1 | a0008c0010t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.163-2693A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305834 | ||||||
| chr12:51305914
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0254a0001c0001t0001g0266 | 4 | HG00639.hp1 HG01978.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2773T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305914 | ||||||
| chr12:51305998
|
G | A | 62 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(59): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-2857C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305998 | ||||||
| chr12:51306035
|
A | C | 1 | a0001c0001t0006g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2894T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306035 | ||||||
| chr12:51306067
|
G | A | 62 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(59): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-2926C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306067 | ||||||
| chr12:51306134
|
T | C | 102 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(99): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.163-2993A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306134 | ||||||
| chr12:51306238
|
T | C | 3 | a0001c0001t0002g0184a0001c0001t0002g0214a0001c0001t0002g0216 | 3 | NA18975.hp1 NA19002.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.163-3097A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306238 | ||||||
| chr12:51306266
|
C | G | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.163-3125G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306266 | ||||||
| chr12:51306305
|
T | A | 1 | a0011c0015t0001g0152 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163-3164A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306305 | ||||||
| chr12:51306356
|
G | A | 40 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(37): Show | 43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.163-3215C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306356 | ||||||
| chr12:51306403
|
G | A | 40 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(37): Show | 43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.163-3262C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306403 | ||||||
| chr12:51306519
|
C | A | 3 | a0003c0003t0001g0369a0003c0003t0001g0370a0003c0003t0001g0371 | 3 | HG02145.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-3378G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306519 | ||||||
| chr12:51306519
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.163-3378G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306519 | ||||||
| chr12:51306553
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-3412C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306553 | ||||||
| chr12:51306630
|
T | A | 62 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(59): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-3489A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306630 | ||||||
| chr12:51306728
|
A | T | 62 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(59): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-3587T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306728 | ||||||
| chr12:51306737
|
C | T | 1 | a0001c0001t0002g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-3596G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306737 | ||||||
| chr12:51306789
|
A | G | 1 | a0001c0004t0001g0016 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.163-3648T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306789 | ||||||
| chr12:51306793
|
T | G | 1 | a0004c0005t0001g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163-3652A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306793 | ||||||
| chr12:51306843
|
T | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(5): Show | 8 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-3702A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306843 | ||||||
| chr12:51307051
|
G | A | 4 | a0002c0007t0001g0027a0002c0007t0001g0028a0002c0007t0001g0031others(1): Show | 4 | NA18978.hp2 NA18988.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-3910C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307051 | ||||||
| chr12:51307073
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-3932T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307073 | ||||||
| chr12:51307141
|
G | A | 102 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(99): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163-4000C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307141 | ||||||
| chr12:51307223
|
C | T | 8 | a0004c0005t0001g0022a0004c0005t0001g0024a0004c0005t0001g0029others(5): Show | 8 | HG00438.hp1 HG00597.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-4082G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307223 | ||||||
| chr12:51307237
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-4096G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307237 | ||||||
| chr12:51307240
|
G | A | 2 | a0002c0002t0001g0060a0002c0002t0001g0061 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.163-4099C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307240 | ||||||
| chr12:51307282
|
C | CA | 5 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0134others(2): Show | 6 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-4142dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307282 | ||||||
| chr12:51307282
|
CA | C | 166 | a0001c0001t0001g0017a0001c0001t0001g0079a0001c0001t0001g0121others(163): Show | 174 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.163-4142delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307282 | ||||||
| chr12:51307282
|
CAA | C | 6 | a0001c0001t0001g0272a0001c0001t0001g0330a0001c0004t0001g0320others(3): Show | 6 | HG01169.hp2 HG02896.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-4143_163-4142d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307282 | ||||||
| chr12:51307371
|
T | A | 102 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(99): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163-4230A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307371 | ||||||
| chr12:51307474
|
C | T | 8 | a0001c0001t0001g0095a0001c0001t0003g0003a0001c0001t0003g0082others(5): Show | 10 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-4333G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307474 | ||||||
| chr12:51307491
|
C | T | 1 | a0001c0004t0001g0360 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.163-4350G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307491 | ||||||
| chr12:51307507
|
A | G | 102 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(99): Show | 111 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.163-4366T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307507 | ||||||
| chr12:51307710
|
C | CA | 26 | a0001c0001t0001g0243a0001c0001t0002g0209a0002c0002t0001g0001others(23): Show | 30 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.163-4570dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307710 | ||||||
| chr12:51307774
|
T | C | 2 | a0004c0005t0001g0052a0004c0005t0001g0054 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.163-4633A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307774 | ||||||
| chr12:51307894
|
G | A | 2 | a0003c0003t0001g0008a0003c0003t0001g0084 | 3 | HG02258.hp1 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.163-4753C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307894 | ||||||
| chr12:51307985
|
C | A | 106 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(103): Show | 115 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.163-4844G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307985 | ||||||
| chr12:51308721
|
G | C | 62 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(59): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.162+5102C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51308721 | ||||||
| chr12:51309049
|
T | C | 5 | a0004c0005t0001g0036a0004c0005t0001g0044a0004c0005t0001g0047others(2): Show | 5 | HG02257.hp2 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+4774A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309049 | ||||||
| chr12:51309130
|
C | A | 106 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(103): Show | 115 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.162+4693G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309130 | ||||||
| chr12:51309360
|
T | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(5): Show | 8 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+4463A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309360 | ||||||
| chr12:51309554
|
AT | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 39 | HG00323.hp1 HG00558.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.162+4268delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309554 | ||||||
| chr12:51309600
|
G | A | 2 | a0002c0002t0001g0060a0002c0002t0001g0061 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.162+4223C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309600 | ||||||
| chr12:51309662
|
T | C | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+4161A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309662 | ||||||
| chr12:51309828
|
T | C | 5 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(2): Show | 5 | NA18949.hp1 NA18959.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+3995A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309828 | ||||||
| chr12:51309977
|
G | T | 6 | a0001c0004t0001g0311a0001c0004t0001g0327a0001c0004t0001g0332others(3): Show | 6 | HG00621.hp2 NA18948.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+3846C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309977 | ||||||
| chr12:51310050
|
A | G | 102 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(99): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.162+3773T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310050 | ||||||
| chr12:51310174
|
T | C | 1 | a0002c0002t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.162+3649A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310174 | ||||||
| chr12:51310187
|
G | A | 6 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+3636C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310187 | ||||||
| chr12:51310262
|
A | T | 17 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(14): Show | 17 | HG02056.hp1 NA18747.hp2 NA18944.hp2 others(14): Show |
intron_variant | MODIFIER | c.162+3561T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310262 | ||||||
| chr12:51310306
|
A | C | 1 | a0001c0001t0002g0226 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.162+3517T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310306 | ||||||
| chr12:51310308
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.162+3515G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310308 | ||||||
| chr12:51310656
|
T | A | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+3167A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310656 | ||||||
| chr12:51310788
|
T | C | 42 | a0002c0002t0001g0034a0002c0002t0001g0055a0002c0002t0001g0056others(39): Show | 44 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.162+3035A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310788 | ||||||
| chr12:51310806
|
A | T | 1 | a0001c0004t0001g0016 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+3017T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310806 | ||||||
| chr12:51311006
|
G | C | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2817C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311006 | ||||||
| chr12:51311041
|
G | A | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2782C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311041 | ||||||
| chr12:51311097
|
C | CT | 69 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0001g0211others(66): Show | 73 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.162+2725dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311097 | ||||||
| chr12:51311097
|
CT | C | 24 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0063others(21): Show | 28 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.162+2725delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311097 | ||||||
| chr12:51311196
|
C | T | 1 | a0001c0004t0001g0016 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+2627G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311196 | ||||||
| chr12:51311302
|
G | A | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2521C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311302 | ||||||
| chr12:51311384
|
C | CTTATTTA | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2438_162+2439i others(9): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311384 | ||||||
| chr12:51311473
|
G | A | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2350C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311473 | ||||||
| chr12:51311567
|
G | C | 1 | a0003c0003t0001g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.162+2256C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311567 | ||||||
| chr12:51311570
|
G | A | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2253C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311570 | ||||||
| chr12:51311622
|
T | C | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2201A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311622 | ||||||
| chr12:51311656
|
C | G | 1 | a0003c0003t0001g0357 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.162+2167G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311656 | ||||||
| chr12:51311712
|
G | T | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2111C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311712 | ||||||
| chr12:51311730
|
A | G | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2093T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311730 | ||||||
| chr12:51311772
|
A | ATT | 65 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(62): Show | 71 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.162+2050_162+2051i others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311772 | ||||||
| chr12:51311773
|
A | T | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2050T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311773 | ||||||
| chr12:51311834
|
C | T | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+1989G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311834 | ||||||
| chr12:51311899
|
A | G | 208 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(205): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.162+1924T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311899 | ||||||
| chr12:51311983
|
G | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0283others(34): Show | 38 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+1840C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311983 | ||||||
| chr12:51312024
|
G | A | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+1799C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312024 | ||||||
| chr12:51312047
|
T | C | 1 | a0001c0001t0001g0353 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.162+1776A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312047 | ||||||
| chr12:51312051
|
C | T | 2 | a0004c0005t0001g0052a0004c0005t0001g0054 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.162+1772G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312051 | ||||||
| chr12:51312196
|
T | G | 3 | a0001c0001t0001g0211a0001c0001t0002g0210a0003c0003t0001g0165 | 3 | HG02109.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162+1627A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312196 | ||||||
| chr12:51312411
|
A | T | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+1412T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312411 | ||||||
| chr12:51312520
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.162+1303G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312520 | ||||||
| chr12:51312683
|
A | G | 1 | a0004c0005t0001g0049 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.162+1140T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312683 | ||||||
| chr12:51312764
|
A | T | 22 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0063others(19): Show | 26 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+1059T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312764 | ||||||
| chr12:51313184
|
G | GAGGA | 20 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0001g0124others(17): Show | 21 | HG01167.hp2 HG01169.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.162+635_162+638dup others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | ||||||
| chr12:51313184
|
G | GAGGAAGG others(1): Show |
108 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0166others(105): Show | 114 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.162+631_162+638dup others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | ||||||
| chr12:51313184
|
G | GAGGAAGG others(5): Show |
42 | a0001c0001t0001g0245a0001c0001t0001g0281a0001c0001t0001g0282others(39): Show | 42 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.162+627_162+638dup others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | ||||||
| chr12:51313184
|
G | GAGGAAGG others(9): Show |
14 | a0001c0001t0001g0223a0001c0001t0001g0336a0001c0001t0001g0337others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.162+623_162+638dup others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | ||||||
| chr12:51313184
|
GAGGA | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG02083.hp1 NA18968.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.162+635_162+638del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | ||||||
| chr12:51313184
|
GAGGAAGG others(5): Show |
G | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0154others(2): Show | 7 | HG02155.hp2 NA18939.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+627_162+638del others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | ||||||
| chr12:51313215
|
G | GAAGGAAG others(9): Show |
1 | a0001c0004t0001g0299 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.162+607_162+608ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313215 | ||||||
| chr12:51313216
|
A | AAGGAAGG others(9): Show |
5 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0237others(2): Show | 6 | HG00423.hp2 HG00738.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+606_162+607ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313216 | ||||||
| chr12:51313216
|
A | AAGGAAGG others(5): Show |
31 | a0001c0001t0001g0019a0001c0001t0001g0235a0001c0001t0001g0236others(28): Show | 32 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.162+606_162+607ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313216 | ||||||
| chr12:51313216
|
A | AAGGAAGG others(5): Show |
1 | a0001c0001t0001g0258 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162+606_162+607ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313216 | ||||||
| chr12:51313220
|
A | AAGGAAGG others(17): Show |
2 | a0002c0002t0001g0021a0002c0002t0002g0076 | 2 | HG02523.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.162+602_162+603ins others(24): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | ||||||
| chr12:51313220
|
A | AAGGAAGG others(13): Show |
15 | a0002c0002t0001g0001a0002c0002t0001g0063a0002c0002t0001g0064others(12): Show | 19 | HG00408.hp2 HG00609.hp1 NA18612.hp2 others(16): Show |
intron_variant | MODIFIER | c.162+602_162+603ins others(20): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | ||||||
| chr12:51313220
|
A | AAGGAAGG others(9): Show |
3 | a0002c0002t0001g0068a0002c0011t0001g0073a0008c0010t0001g0053 | 3 | HG02970.hp1 NA18943.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.162+602_162+603ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | ||||||
| chr12:51313220
|
A | AAGGAAGG others(13): Show |
1 | a0002c0002t0002g0067 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.162+602_162+603ins others(20): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | ||||||
| chr12:51313220
|
A | AAGGAAGG others(5): Show |
3 | a0001c0004t0001g0359a0002c0002t0002g0075a0003c0003t0001g0346 | 3 | HG01192.hp1 NA19083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.162+602_162+603ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | ||||||
| chr12:51313220
|
A | C | 1 | a0001c0001t0003g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.162+603T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | ||||||
| chr12:51313224
|
C | A | 36 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0007t0001g0027others(33): Show | 37 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.162+599G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313224 | ||||||
| chr12:51313228
|
A | AAGGAAGG others(5): Show |
1 | a0004c0005t0001g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162+594_162+595ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313228 | ||||||
| chr12:51313228
|
A | AAGGC | 6 | a0001c0004t0001g0261a0004c0005t0001g0036a0004c0005t0001g0044others(3): Show | 6 | HG02257.hp2 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+591_162+594dup others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313228 | ||||||
| chr12:51313228
|
A | AAGGCAGG others(1): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0266a0001c0001t0006g0270 | 4 | HG01433.hp2 HG01496.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+587_162+594dup others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313228 | ||||||
| chr12:51313228
|
A | C | 77 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(74): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.162+595T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313228 | ||||||
| chr12:51313307
|
C | T | 67 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0276others(64): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.162+516G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313307 | ||||||
| chr12:51313346
|
C | CT | 102 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(99): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.162+476dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313346 | ||||||
| chr12:51313593
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0106others(3): Show | 8 | HG02155.hp2 NA18939.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.162+230C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313593 | ||||||
| chr12:51313593
|
G | C | 1 | a0001c0001t0001g0017 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.162+230C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313593 | ||||||
| chr12:51313698
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.162+125T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313698 | ||||||
| chr12:51314017
|
C | CTTAT | 26 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0086others(23): Show | 26 | HG00639.hp2 HG01070.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.82-118_82-115dupAT others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | ||||||
| chr12:51314017
|
CTTAT | C | 184 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 195 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.82-118_82-115delAT others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | ||||||
| chr12:51314017
|
CTTATTTA others(1): Show |
C | 114 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0100others(111): Show | 124 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.82-122_82-115delAT others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | ||||||
| chr12:51314017
|
CTTATTTA others(5): Show |
C | 6 | a0001c0001t0001g0107a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | NA18939.hp2 NA18948.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-126_82-115delAT others(10): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | ||||||
| chr12:51314017
|
CTTATTTA others(9): Show |
C | 1 | a0001c0001t0001g0350 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.82-130_82-115delAT others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | ||||||
| chr12:51314021
|
T | C | 1 | a0009c0017t0001g0366 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.82-118A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314021 | ||||||
| chr12:51314070
|
C | T | 22 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0063others(19): Show | 26 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.82-167G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314070 | ||||||
| chr12:51314080
|
C | G | 1 | a0011c0015t0001g0152 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.82-177G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314080 | ||||||
| chr12:51314129
|
C | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0002g0222 | 3 | HG02572.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.82-226G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314129 | ||||||
| chr12:51314132
|
T | C | 107 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(104): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.82-229A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314132 | ||||||
| chr12:51314199
|
C | T | 6 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-296G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314199 | ||||||
| chr12:51314204
|
C | T | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-301G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314204 | ||||||
| chr12:51314237
|
G | A | 32 | a0002c0007t0001g0027a0002c0007t0001g0028a0002c0007t0001g0031others(29): Show | 33 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.82-334C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314237 | ||||||
| chr12:51314413
|
C | T | 1 | a0002c0002t0002g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.82-510G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314413 | ||||||
| chr12:51314435
|
A | G | 52 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0001g0211others(49): Show | 56 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.82-532T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314435 | ||||||
| chr12:51314521
|
T | C | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-618A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314521 | ||||||
| chr12:51314540
|
T | C | 209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(206): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.82-637A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314540 | ||||||
| chr12:51314542
|
G | C | 1 | a0001c0001t0001g0160 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.82-639C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314542 | ||||||
| chr12:51314597
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-694G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314597 | ||||||
| chr12:51314714
|
G | A | 2 | a0001c0001t0001g0321a0001c0001t0001g0331 | 2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.82-811C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314714 | ||||||
| chr12:51314753
|
C | T | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-850G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314753 | ||||||
| chr12:51314780
|
C | T | 42 | a0002c0002t0001g0034a0002c0002t0001g0055a0002c0002t0001g0056others(39): Show | 44 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-877G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314780 | ||||||
| chr12:51314799
|
C | CA | 43 | a0001c0001t0002g0180a0002c0002t0001g0034a0002c0002t0001g0055others(40): Show | 45 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.82-897dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314799 | ||||||
| chr12:51314799
|
C | CAA | 20 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0063others(17): Show | 24 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-898_82-897dupTT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314799 | ||||||
| chr12:51314821
|
T | G | 108 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(105): Show | 117 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.82-918A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314821 | ||||||
| chr12:51314930
|
A | G | 13 | a0002c0007t0001g0027a0002c0007t0001g0028a0002c0007t0001g0031others(10): Show | 13 | HG00438.hp1 HG00597.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-1027T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314930 | ||||||
| chr12:51314962
|
T | TC | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-1060dupG | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314962 | ||||||
| chr12:51315099
|
T | C | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-1196A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315099 | ||||||
| chr12:51315174
|
A | ATT | 19 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0066others(16): Show | 23 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.82-1273_82-1272dup others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315174 | ||||||
| chr12:51315174
|
A | T | 49 | a0001c0001t0001g0010a0001c0001t0001g0154a0001c0001t0001g0166others(46): Show | 51 | HG00558.hp2 HG00597.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-1271T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315174 | ||||||
| chr12:51315174
|
AT | A | 45 | a0001c0001t0001g0244a0001c0009t0002g0181a0002c0002t0001g0034others(42): Show | 47 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.82-1272delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315174 | ||||||
| chr12:51315177
|
T | A | 29 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0080others(26): Show | 30 | HG00639.hp2 HG01175.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.82-1274A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315177 | ||||||
| chr12:51315178
|
T | A | 11 | a0002c0002t0001g0034a0002c0002t0001g0059a0002c0002t0001g0060others(8): Show | 12 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-1275A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315178 | ||||||
| chr12:51315180
|
T | A | 8 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(5): Show | 8 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-1277A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315180 | ||||||
| chr12:51315207
|
T | C | 1 | a0001c0004t0001g0328 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.82-1304A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315207 | ||||||
| chr12:51315297
|
T | G | 6 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-1394A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315297 | ||||||
| chr12:51315319
|
C | A | 6 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-1416G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315319 | ||||||
| chr12:51315328
|
G | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.82-1425C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315328 | ||||||
| chr12:51315378
|
T | C | 101 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(98): Show | 103 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.82-1475A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315378 | ||||||
| chr12:51315395
|
A | C | 1 | a0004c0006t0001g0023 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.82-1492T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315395 | ||||||
| chr12:51315423
|
C | T | 2 | a0004c0005t0001g0052a0004c0005t0001g0054 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.82-1520G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315423 | ||||||
| chr12:51315498
|
T | C | 41 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(38): Show | 44 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.82-1595A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315498 | ||||||
| chr12:51315538
|
G | A | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-1635C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315538 | ||||||
| chr12:51315633
|
G | T | 1 | a0001c0001t0006g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.82-1730C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315633 | ||||||
| chr12:51315661
|
G | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG00140.hp1 HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.82-1758C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315661 | ||||||
| chr12:51315667
|
C | T | 12 | a0001c0001t0001g0287a0001c0001t0001g0293a0001c0001t0001g0330others(9): Show | 12 | HG02145.hp1 HG02559.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-1764G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315667 | ||||||
| chr12:51315706
|
T | A | 67 | a0001c0001t0002g0020a0002c0002t0001g0001a0002c0002t0001g0021others(64): Show | 73 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.82-1803A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315706 | ||||||
| chr12:51315871
|
C | A | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-1968G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315871 | ||||||
| chr12:51316048
|
ACCAT | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0254a0001c0001t0001g0266 | 4 | HG00639.hp1 HG01978.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-2149_82-2146del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316048 | ||||||
| chr12:51316218
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.82-2315G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316218 | ||||||
| chr12:51316290
|
C | T | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-2387G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316290 | ||||||
| chr12:51316328
|
C | CA | 149 | a0001c0001t0001g0079a0001c0001t0001g0089a0001c0001t0001g0090others(146): Show | 159 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.82-2426dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316328 | ||||||
| chr12:51316328
|
C | CAA | 93 | a0001c0001t0001g0017a0001c0001t0001g0150a0001c0001t0001g0151others(90): Show | 95 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.82-2427_82-2426dup others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316328 | ||||||
| chr12:51316328
|
C | CAAA | 18 | a0001c0001t0001g0163a0001c0001t0001g0277a0001c0001t0001g0286others(15): Show | 18 | HG00099.hp1 HG00642.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.82-2428_82-2426dup others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316328 | ||||||
| chr12:51316328
|
CA | C | 40 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(37): Show | 43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.82-2426delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316328 | ||||||
| chr12:51316422
|
T | G | 284 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(281): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.82-2519A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316422 | ||||||
| chr12:51316482
|
G | A | 2 | a0004c0005t0001g0052a0004c0005t0001g0054 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.82-2579C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316482 | ||||||
| chr12:51316561
|
A | C | 67 | a0001c0001t0002g0020a0002c0002t0001g0001a0002c0002t0001g0021others(64): Show | 73 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.82-2658T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316561 | ||||||
| chr12:51316695
|
C | T | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-2792G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316695 | ||||||
| chr12:51317267
|
A | G | 53 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0001g0211others(50): Show | 57 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.82-3364T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317267 | ||||||
| chr12:51317316
|
T | G | 1 | a0002c0011t0001g0073 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.82-3413A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317316 | ||||||
| chr12:51317341
|
G | C | 3 | a0001c0001t0002g0226a0003c0003t0001g0225a0003c0003t0001g0233 | 3 | HG02559.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.82-3438C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317341 | ||||||
| chr12:51317352
|
G | C | 1 | a0003c0003t0001g0153 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.82-3449C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317352 | ||||||
| chr12:51317365
|
T | C | 1 | a0002c0002t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-3462A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317365 | ||||||
| chr12:51317559
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 38 | HG00323.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.82-3656G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317559 | ||||||
| chr12:51317613
|
C | T | 1 | a0001c0001t0006g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.82-3710G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317613 | ||||||
| chr12:51317676
|
T | C | 1 | a0010c0016t0001g0094 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.82-3773A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317676 | ||||||
| chr12:51317711
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.82-3808C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317711 | ||||||
| chr12:51317779
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82-3876C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317779 | ||||||
| chr12:51317839
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82-3936A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317839 | ||||||
| chr12:51317950
|
C | T | 66 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0034others(63): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-4047G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317950 | ||||||
| chr12:51318121
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.82-4218G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318121 | ||||||
| chr12:51318233
|
G | A | 1 | a0001c0001t0001g0356 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.82-4330C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318233 | ||||||
| chr12:51318262
|
C | CT | 102 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0245others(99): Show | 104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.82-4360dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318262 | ||||||
| chr12:51318390
|
T | C | 1 | a0002c0002t0001g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-4487A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318390 | ||||||
| chr12:51318465
|
T | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0154others(2): Show | 7 | HG02155.hp2 NA18939.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-4562A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318465 | ||||||
| chr12:51318468
|
G | A | 1 | a0001c0001t0001g0017 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.82-4565C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318468 | ||||||
| chr12:51318479
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.82-4576G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318479 | ||||||
| chr12:51318535
|
T | C | 115 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(112): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.82-4632A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318535 | ||||||
| chr12:51318559
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-4656C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318559 | ||||||
| chr12:51318774
|
A | T | 1 | a0001c0001t0002g0093 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.82-4871T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318774 | ||||||
| chr12:51318817
|
G | A | 1 | a0001c0001t0004g0157 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.82-4914C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318817 | ||||||
| chr12:51318896
|
TTTTGGTT others(12): Show |
T | 4 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG01070.hp2 HG02735.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-5012_82-4994del others(19): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318896 | ||||||
| chr12:51318957
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.82-5054G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318957 | ||||||
| chr12:51319130
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.81+4892A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319130 | ||||||
| chr12:51319267
|
C | T | 26 | a0002c0007t0001g0027a0002c0007t0001g0031a0002c0007t0001g0062others(23): Show | 27 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.81+4755G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319267 | ||||||
| chr12:51319272
|
G | C | 1 | a0001c0001t0003g0158 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.81+4750C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319272 | ||||||
| chr12:51319399
|
T | C | 52 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(49): Show | 54 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.81+4623A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319399 | ||||||
| chr12:51319421
|
G | A | 2 | a0004c0005t0001g0052a0004c0005t0001g0054 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.81+4601C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319421 | ||||||
| chr12:51319646
|
A | G | 217 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(214): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.81+4376T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319646 | ||||||
| chr12:51319802
|
C | T | 283 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(280): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.81+4220G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319802 | ||||||
| chr12:51319921
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.81+4101C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319921 | ||||||
| chr12:51319953
|
T | C | 4 | a0002c0007t0001g0027a0002c0007t0001g0028a0002c0007t0001g0031others(1): Show | 4 | NA18978.hp2 NA18988.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+4069A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319953 | ||||||
| chr12:51319955
|
C | CTCTCCTT others(7): Show |
4 | a0002c0007t0001g0027a0002c0007t0001g0028a0002c0007t0001g0031others(1): Show | 4 | NA18978.hp2 NA18988.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+4066_81+4067ins others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319955 | ||||||
| chr12:51319955
|
C | CTCTCTCC others(9): Show |
209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(206): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.81+4066_81+4067ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319955 | ||||||
| chr12:51319982
|
C | T | 213 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(210): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+4040G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319982 | ||||||
| chr12:51319985
|
C | G | 101 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0276others(98): Show | 103 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.81+4037G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319985 | ||||||
| chr12:51320162
|
G | A | 7 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+3860C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320162 | ||||||
| chr12:51320631
|
ATTC | A | 90 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0276others(87): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.81+3388_81+3390del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320631 | ||||||
| chr12:51320631
|
ATTCT | A | 6 | a0003c0003t0001g0295a0003c0003t0001g0296a0003c0003t0001g0297others(3): Show | 6 | HG02145.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+3387_81+3390del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320631 | ||||||
| chr12:51320634
|
C | CT | 7 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0087others(4): Show | 7 | HG00323.hp1 NA18955.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+3387dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320634 | ||||||
| chr12:51320634
|
CT | C | 11 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(8): Show | 11 | HG01070.hp1 HG01993.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+3387delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320634 | ||||||
| chr12:51320634
|
CTTT | C | 46 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(43): Show | 48 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.81+3385_81+3387del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320634 | ||||||
| chr12:51320634
|
CTTTT | C | 23 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0063others(20): Show | 27 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.81+3384_81+3387del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320634 | ||||||
| chr12:51320636
|
T | A | 2 | a0001c0001t0001g0356a0001c0004t0001g0307 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.81+3386A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320636 | ||||||
| chr12:51320637
|
T | A | 90 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0276others(87): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.81+3385A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320637 | ||||||
| chr12:51320638
|
T | A | 6 | a0003c0003t0001g0295a0003c0003t0001g0296a0003c0003t0001g0297others(3): Show | 6 | HG02145.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+3384A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320638 | ||||||
| chr12:51320639
|
T | A | 1 | a0001c0004t0001g0307 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.81+3383A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320639 | ||||||
| chr12:51320640
|
T | A | 33 | a0001c0001t0001g0017a0001c0001t0001g0163a0001c0001t0001g0283others(30): Show | 35 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.81+3382A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320640 | ||||||
| chr12:51320641
|
T | A | 6 | a0003c0003t0001g0295a0003c0003t0001g0296a0003c0003t0001g0297others(3): Show | 6 | HG02145.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+3381A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320641 | ||||||
| chr12:51320644
|
T | A | 1 | a0003c0003t0001g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.81+3378A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320644 | ||||||
| chr12:51320786
|
T | A | 172 | a0001c0001t0001g0017a0001c0001t0001g0079a0001c0001t0001g0163others(169): Show | 180 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.81+3236A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320786 | ||||||
| chr12:51320801
|
AGAG | A | 6 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+3218_81+3220del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320801 | ||||||
| chr12:51320934
|
A | AAC | 7 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0059others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACAC | 8 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0372others(5): Show | 8 | HG01346.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACAC | 6 | a0001c0001t0001g0079a0001c0001t0001g0272a0001c0001t0006g0270others(3): Show | 6 | HG00408.hp2 HG01192.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(1): Show |
17 | a0001c0001t0001g0271a0001c0001t0001g0358a0002c0002t0001g0001others(14): Show | 21 | HG00609.hp1 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(3): Show |
4 | a0001c0001t0001g0015a0002c0002t0001g0066a0002c0002t0002g0067others(1): Show | 5 | HG00438.hp2 HG02055.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(10): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(5): Show |
12 | a0001c0001t0001g0019a0001c0001t0001g0262a0001c0001t0001g0263others(9): Show | 12 | HG01515.hp1 HG01978.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(7): Show |
21 | a0001c0001t0001g0163a0001c0001t0001g0235a0001c0001t0001g0258others(18): Show | 21 | HG00099.hp1 HG01071.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(19): Show |
1 | a0001c0001t0001g0356 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(26): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(9): Show |
21 | a0001c0001t0001g0018a0001c0001t0001g0250a0001c0001t0001g0251others(18): Show | 21 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(11): Show |
22 | a0001c0001t0001g0014a0001c0001t0001g0245a0001c0001t0001g0246others(19): Show | 23 | HG00099.hp2 HG00642.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(18): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(13): Show |
16 | a0001c0001t0001g0017a0001c0001t0001g0241a0001c0001t0001g0242others(13): Show | 18 | HG01071.hp1 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(20): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(15): Show |
11 | a0001c0001t0001g0239a0001c0001t0001g0314a0001c0004t0001g0311others(8): Show | 12 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(22): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(17): Show |
13 | a0001c0001t0001g0237a0001c0001t0001g0304a0001c0004t0001g0305others(10): Show | 13 | HG00609.hp2 HG01891.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(24): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(19): Show |
11 | a0001c0001t0001g0277a0001c0001t0001g0298a0001c0001t0001g0300others(8): Show | 11 | HG00733.hp2 HG01346.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(26): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(21): Show |
15 | a0001c0001t0001g0289a0001c0001t0001g0293a0001c0001t0001g0294others(12): Show | 15 | HG00741.hp2 HG02886.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(28): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(23): Show |
4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | HG01496.hp2 NA18951.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(30): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(25): Show |
1 | a0001c0001t0001g0284 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(32): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(27): Show |
3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0004t0001g0016 | 4 | HG03491.hp1 HG03492.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(34): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | AACACACA others(29): Show |
1 | a0001c0001t0001g0280 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(36): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | ACACACAC others(6): Show |
1 | a0005c0008t0001g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(13): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | ACACACAC others(12): Show |
1 | a0006c0014t0001g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(19): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | ACACACAC others(14): Show |
3 | a0001c0001t0001g0238a0001c0004t0001g0310a0004c0005t0001g0036 | 3 | HG01070.hp1 HG02257.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(21): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | ACACACAC others(18): Show |
1 | a0003c0003t0001g0297 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(25): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | ACACACAC others(24): Show |
2 | a0001c0001t0001g0283a0001c0001t0001g0376 | 2 | HG00735.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(31): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320934
|
A | C | 1 | a0002c0002t0001g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.81+3088T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | ||||||
| chr12:51320936
|
A | C | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.81+3086T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320936 | ||||||
| chr12:51320941
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.81+3080_81+3081ins others(13): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320941 | ||||||
| chr12:51320954
|
A | C | 213 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(210): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+3068T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320954 | ||||||
| chr12:51320971
|
T | A | 213 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(210): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+3051A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320971 | ||||||
| chr12:51321099
|
T | G | 1 | a0002c0007t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.81+2923A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321099 | ||||||
| chr12:51321135
|
TGAGA | T | 171 | a0001c0001t0001g0017a0001c0001t0001g0079a0001c0001t0001g0163others(168): Show | 179 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.81+2883_81+2886del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321135 | ||||||
| chr12:51321194
|
G | A | 18 | a0002c0002t0001g0001a0002c0002t0001g0021a0002c0002t0001g0063others(15): Show | 22 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.81+2828C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321194 | ||||||
| chr12:51321370
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.81+2652C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321370 | ||||||
| chr12:51321565
|
G | A | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.81+2457C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321565 | ||||||
| chr12:51321616
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.81+2406G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321616 | ||||||
| chr12:51321823
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.81+2199T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321823 | ||||||
| chr12:51321861
|
T | C | 1 | a0001c0001t0006g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+2161A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321861 | ||||||
| chr12:51321876
|
CTT | C | 3 | a0002c0002t0002g0007a0002c0002t0002g0075a0002c0002t0002g0076 | 4 | NA18982.hp1 NA18995.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+2144_81+2145del others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321876 | ||||||
| chr12:51321897
|
T | G | 171 | a0001c0001t0001g0017a0001c0001t0001g0079a0001c0001t0001g0163others(168): Show | 179 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.81+2125A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321897 | ||||||
| chr12:51321930
|
G | T | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(209): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.81+2092C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321930 | ||||||
| chr12:51322012
|
G | T | 1 | a0001c0001t0002g0184 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.81+2010C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322012 | ||||||
| chr12:51322146
|
ACT | A | 42 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(39): Show | 45 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.81+1874_81+1875del others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322146 | ||||||
| chr12:51322159
|
T | C | 1 | a0002c0002t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.81+1863A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322159 | ||||||
| chr12:51322178
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.81+1844T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322178 | ||||||
| chr12:51322390
|
A | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+1632T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322390 | ||||||
| chr12:51322398
|
G | T | 376 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(373): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.81+1624C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322398 | ||||||
| chr12:51322440
|
A | AGTGTG | 2 | a0003c0003t0001g0008a0003c0003t0001g0084 | 3 | HG02258.hp1 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.81+1577_81+1581dup others(5): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322440 | ||||||
| chr12:51322550
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.81+1472G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322550 | ||||||
| chr12:51322607
|
G | GT | 21 | a0001c0001t0001g0080a0001c0001t0001g0166a0001c0001t0002g0002others(18): Show | 24 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.81+1414dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322607 | ||||||
| chr12:51322607
|
G | T | 1 | a0001c0001t0003g0082 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.81+1415C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322607 | ||||||
| chr12:51322607
|
GT | G | 213 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(210): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+1414delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322607 | ||||||
| chr12:51322614
|
T | G | 171 | a0001c0001t0001g0017a0001c0001t0001g0079a0001c0001t0001g0163others(168): Show | 179 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.81+1408A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322614 | ||||||
| chr12:51322627
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.81+1395G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322627 | ||||||
| chr12:51322700
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.81+1322G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322700 | ||||||
| chr12:51322797
|
CTT | C | 213 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(210): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+1223_81+1224del others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322797 | ||||||
| chr12:51322809
|
C | T | 2 | a0001c0001t0001g0367a0001c0001t0001g0376 | 2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.81+1213G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322809 | ||||||
| chr12:51322920
|
C | T | 1 | a0003c0003t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.81+1102G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322920 | ||||||
| chr12:51322982
|
G | A | 170 | a0001c0001t0001g0017a0001c0001t0001g0079a0001c0001t0001g0271others(167): Show | 178 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.81+1040C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322982 | ||||||
| chr12:51323297
|
G | A | 1 | a0004c0005t0001g0078 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.81+725C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323297 | ||||||
| chr12:51323310
|
C | T | 1 | a0003c0003t0001g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.81+712G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323310 | ||||||
| chr12:51323400
|
T | TCTGAACA others(33): Show |
9 | a0001c0001t0001g0017a0001c0001t0001g0367a0001c0001t0001g0372others(6): Show | 10 | HG01891.hp2 HG02145.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+582_81+621dupGA others(38): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323400 | ||||||
| chr12:51323462
|
G | C | 285 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(282): Show | 300 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.81+560C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323462 | ||||||
| chr12:51323463
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.81+559T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323463 | ||||||
| chr12:51323487
|
T | C | 1 | a0001c0001t0003g0374 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.81+535A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323487 | ||||||
| chr12:51323490
|
G | C | 1 | a0007c0020t0001g0375 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.81+532C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323490 | ||||||
| chr12:51323525
|
C | G | 63 | a0001c0001t0002g0020a0002c0002t0001g0001a0002c0002t0001g0021others(60): Show | 69 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.81+497G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323525 | ||||||
| chr12:51323641
|
T | G | 1 | a0001c0001t0001g0376 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.81+381A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323641 | ||||||
| chr12:51323754
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.81+268G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323754 | ||||||
| chr12:51323817
|
G | A | 1 | a0003c0003t0001g0377 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81+205C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323817 |