| geneid | 222389 |
|---|---|
| ensemblid | ENSG00000165626.19 |
| hgncid | 23514 |
| symbol | BEND7 |
| name | BEN domain containing 7 |
| refseq_nuc | NM_001369863.1 |
| refseq_prot | NP_001356792.1 |
| ensembl_nuc | ENST00000466271.3 |
| ensembl_prot | ENSP00000507500.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 13441088 |
| end | 13529014 |
| strand | - |
| ver | v1.2 |
| region | chr10:13441088-13529014 |
| region5000 | chr10:13436088-13534014 |
| regionname0 | BEND7_chr10_13441088_13529014 |
| regionname5000 | BEND7_chr10_13436088_13534014 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 413 | 294 | 83 | 68 | 97 | 10 | 34 | 71 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0002 | 0/0 | 413 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0003 | 0/0 | 413 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0004 | 0/0 | 413 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0005 | 0/0 | 413 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| 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 | 0/0 | 1242 | 149 | 36 | 42 | 43 | 6 | 22 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0002 | 0/1 | 1242 | 62 | 0 | 16 | 34 | 3 | 8 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0003 | 1/0 | 1242 | 55 | 38 | 5 | 8 | 0 | 3 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0004 | 0/0 | 1242 | 23 | 6 | 5 | 10 | 1 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0005 | 0/0 | 1242 | 3 | 3 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0006 | 0/0 | 1242 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0007 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0008 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0009 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0010 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0011 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| c0012 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| 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 | 0/1 | 1122 | 228 | 58 | 61 | 83 | 9 | 16 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0002 | 0/0 | 1131 | 28 | 8 | 5 | 7 | 1 | 7 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0003 | 0/0 | 1122 | 13 | 0 | 0 | 4 | 0 | 9 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0004 | 0/0 | 1123 | 8 | 8 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0005 | 0/0 | 1125 | 6 | 6 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0006 | 0/0 | 1122 | 4 | 0 | 0 | 3 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0007 | 0/0 | 1137 | 3 | 3 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0008 | 0/0 | 1132 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0009 | 1/0 | 1137 | 2 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0010 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0011 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0012 | 0/0 | 1122 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0013 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0014 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| t0015 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| 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 | 1 | 3 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| 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 | 0/0 | 1242 | 149 | 36 | 42 | 43 | 6 | 22 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0002 | 0/1 | 1242 | 62 | 0 | 16 | 34 | 3 | 8 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0003 | 1/0 | 1242 | 55 | 38 | 5 | 8 | 0 | 3 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0004 | 0/0 | 1242 | 23 | 6 | 5 | 10 | 1 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0006 | 0/0 | 1242 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0007 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0008 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0011 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0002c0005 | 0/0 | 1242 | 3 | 3 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0003c0009 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0004c0010 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0005c0012 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2363 | 111 | 31 | 37 | 31 | 5 | 7 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0001t0002 | 0/0 | 2372 | 19 | 1 | 5 | 5 | 1 | 7 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0001t0003 | 0/0 | 2363 | 11 | 0 | 0 | 4 | 0 | 7 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0001t0004 | 0/0 | 2364 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0001t0005 | 0/0 | 2366 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0001t0006 | 0/0 | 2363 | 4 | 0 | 0 | 3 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0001t0010 | 0/0 | 2366 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0002t0001 | 0/1 | 2363 | 59 | 0 | 16 | 33 | 3 | 6 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0002t0003 | 0/0 | 2363 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0002t0012 | 0/0 | 2363 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0002t0015 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0003t0001 | 0/0 | 2363 | 35 | 21 | 3 | 8 | 0 | 3 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0003t0002 | 0/0 | 2372 | 3 | 3 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0003t0004 | 0/0 | 2364 | 4 | 4 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0003t0005 | 0/0 | 2366 | 5 | 5 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0003t0007 | 0/0 | 2378 | 3 | 3 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0003t0008 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0003t0009 | 1/0 | 2378 | 2 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0003t0013 | 0/0 | 2363 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0004t0001 | 0/0 | 2363 | 19 | 5 | 5 | 8 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0004t0002 | 0/0 | 2372 | 2 | 0 | 0 | 2 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0004t0003 | 0/0 | 2363 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0004t0011 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0006t0004 | 0/0 | 2364 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0007t0002 | 0/0 | 2372 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0008t0001 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0001c0011t0001 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0002c0005t0002 | 0/0 | 2372 | 3 | 3 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0003c0009t0001 | 0/0 | 2363 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0004c0010t0001 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| a0005c0012t0014 | 0/0 | 2363 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | copy fasta | chr10 | 13436088 | 13534014 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0001t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0012g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0002t0015g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0009g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0009g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0003t0013g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0004t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0006t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0006t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0007t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0008t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0001c0011t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0002c0005t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0002c0005t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0002c0005t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0003c0009t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0004c0010t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| a0005c0012t0014g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0050 | EUR | GBR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | FIN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0156 | EUR | FIN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00558 | hp1 | a0001 | c0004 | t0001 | g0227 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00609 | hp1 | a0001 | c0004 | t0002 | g0266 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0101 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00673 | hp1 | a0001 | c0004 | t0001 | g0209 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01070 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01081 | hp2 | a0001 | c0003 | t0013 | g0107 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0081 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01243 | hp2 | a0001 | c0003 | t0009 | g0274 | AMR | PUR | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01258 | hp2 | a0001 | c0004 | t0001 | g0203 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0238 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0134 | EUR | IBS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0129 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01891 | hp1 | a0002 | c0005 | t0002 | g0245 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01891 | hp2 | a0004 | c0010 | t0001 | g0119 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0193 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0185 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0148 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0102 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02055 | hp1 | a0001 | c0003 | t0004 | g0110 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0115 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02135 | hp2 | a0001 | c0004 | t0001 | g0063 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | CDX | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0124 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0021 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0128 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | KHV | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0111 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0043 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0249 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02622 | hp2 | a0001 | c0003 | t0005 | g0020 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0177 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02723 | hp1 | a0001 | c0003 | t0005 | g0019 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02809 | hp1 | a0001 | c0007 | t0002 | g0242 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02818 | hp1 | a0001 | c0003 | t0008 | g0248 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0247 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02896 | hp1 | a0002 | c0005 | t0002 | g0243 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0223 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0126 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02922 | hp2 | a0001 | c0004 | t0011 | g0024 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0224 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0127 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02976 | hp2 | a0001 | c0003 | t0004 | g0113 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0023 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03098 | hp1 | a0005 | c0012 | t0014 | g0273 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03098 | hp2 | a0001 | c0003 | t0005 | g0017 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03139 | hp1 | a0001 | c0003 | t0004 | g0114 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03209 | hp2 | a0001 | c0006 | t0004 | g0105 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0222 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0130 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03453 | hp1 | a0002 | c0005 | t0002 | g0244 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03453 | hp2 | a0001 | c0003 | t0007 | g0270 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0109 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0120 | AFR | ESN | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | GWD | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0178 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0046 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03834 | hp2 | a0001 | c0004 | t0003 | g0025 | SAS | BEB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | BEB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0103 | SAS | BEB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0108 | SAS | STU | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | STU | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | BEB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG04184 | hp2 | a0001 | c0002 | t0012 | g0153 | SAS | BEB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0167 | SAS | STU | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | STU | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0034 | SAS | STU | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18522 | hp2 | a0001 | c0003 | t0007 | g0272 | AFR | YRI | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18906 | hp2 | a0001 | c0003 | t0005 | g0018 | AFR | YRI | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18939 | hp1 | a0001 | c0004 | t0001 | g0200 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18944 | hp2 | a0001 | c0011 | t0001 | g0218 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18959 | hp2 | a0001 | c0004 | t0001 | g0205 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18962 | hp2 | a0001 | c0002 | t0015 | g0276 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0164 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0234 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18989 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18991 | hp2 | a0003 | c0009 | t0001 | g0212 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18997 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18999 | hp1 | a0001 | c0004 | t0001 | g0041 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | LWK | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | LWK | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19063 | hp2 | a0001 | c0004 | t0001 | g0237 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19088 | hp2 | a0001 | c0004 | t0002 | g0255 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA19240 | hp2 | a0001 | c0003 | t0008 | g0251 | AFR | YRI | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA20129 | hp1 | a0001 | c0006 | t0004 | g0106 | AFR | ASW | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0188 | EUR | TSI | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | TSI | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0186 | SAS | GIH | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | GIH | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02486 | hp2 | a0001 | c0003 | t0007 | g0271 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0250 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | USA | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18955 | hp1 | a0001 | c0008 | t0001 | g0104 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | USA | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0169 | REF | REF | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0009 | g0275 | REF | REF | BEND7_chr10_13436088_13534014 | BEND7 | chr10 | 13436088 | 13534014 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:13492655
|
G | A | 1 | a0002 | 3 | HG01891.hp1 HG02896.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.793C>T | p.Arg265Cys | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/9 | 1274/2378 | 793/1242 | 265/413 | chr10 | 13492655 | ||
| chr10:13496851
|
G | C | 1 | a0003 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.486C>G | p.Asn162Lys | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/9 | 967/2378 | 486/1242 | 162/413 | chr10 | 13496851 | ||
| chr10:13500012
|
G | A | 1 | a0004 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.214C>T | p.Arg72Trp | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/9 | 695/2378 | 214/1242 | 72/413 | chr10 | 13500012 | ||
| chr10:13526182
|
T | C | 1 | a0005 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.101A>G | p.Asn34Ser | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/9 | 582/2378 | 101/1242 | 34/413 | chr10 | 13526182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:13447279
|
A | G | 1 | a0001c0008 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.1221T>C | p.Ala407Ala | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/9 | 1702/2378 | 1221/1242 | 407/413 | chr10 | 13447279 | ||
| chr10:13452594
|
T | C | 2 | a0001c0002a0001c0004 | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
synonymous_variant | LOW | c.1128A>G | p.Val376Val | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/9 | 1609/2378 | 1128/1242 | 376/413 | chr10 | 13452594 | ||
| chr10:13492617
|
G | A | 1 | a0001c0006 | 2 | HG03209.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.831C>T | p.Ser277Ser | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/9 | 1312/2378 | 831/1242 | 277/413 | chr10 | 13492617 | ||
| chr10:13492851
|
A | G | 6 | a0001c0001a0001c0004a0001c0007others(3): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
synonymous_variant | LOW | c.597T>C | p.Pro199Pro | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/9 | 1078/2378 | 597/1242 | 199/413 | chr10 | 13492851 | ||
| chr10:13499788
|
C | T | 1 | a0001c0007 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.438G>A | p.Thr146Thr | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/9 | 919/2378 | 438/1242 | 146/413 | chr10 | 13499788 | ||
| chr10:13500061
|
T | A | 1 | a0001c0011 | 1 | NA18944.hp2 | synonymous_variant | LOW | c.165A>T | p.Ile55Ile | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/9 | 646/2378 | 165/1242 | 55/413 | chr10 | 13500061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:13441117
|
C | T | 1 | a0001c0002t0012 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*626G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 626 | chr10 | 13441117 | |||||
| chr10:13441156
|
A | G | 1 | a0001c0001t0006 | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*587T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 587 | chr10 | 13441156 | |||||
| chr10:13441207
|
T | C | 1 | a0001c0003t0013 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*536A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 536 | chr10 | 13441207 | |||||
| chr10:13441227
|
A | T | 1 | a0001c0001t0010 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*516T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 516 | chr10 | 13441227 | |||||
| chr10:13441297
|
A | AT | 4 | a0001c0001t0004a0001c0003t0004a0001c0003t0008others(1): Show | 10 | HG02055.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*445dupA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 445 | chr10 | 13441297 | |||||
| chr10:13441398
|
G | A | 1 | a0001c0001t0006 | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*345C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 345 | chr10 | 13441398 | |||||
| chr10:13441560
|
A | G | 1 | a0001c0001t0006 | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*183T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 183 | chr10 | 13441560 | |||||
| chr10:13441634
|
C | T | 1 | a0001c0001t0006 | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*109G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 109 | chr10 | 13441634 | |||||
| chr10:13441688
|
G | A | 1 | a0001c0001t0006 | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*55C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 55 | chr10 | 13441688 | |||||
| chr10:13441726
|
T | C | 1 | a0001c0001t0006 | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*17A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 9/9 | 17 | chr10 | 13441726 | |||||
| chr10:13528569
|
GGCGGCAG others(8): Show |
G | 23 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(20): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
5_prime_UTR_variant | MODIFIER | c.-51_-37delTGCCGCCG others(7): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/9 | 37 | chr10 | 13528569 | |||||
| chr10:13528578
|
GGCGGCA | G | 6 | a0001c0001t0002a0001c0003t0002a0001c0003t0008others(3): Show | 30 | HG00609.hp1 HG01167.hp2 HG01168.hp1 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-51_-46delTGCCGC | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/9 | 46 | chr10 | 13528578 | |||||
| chr10:13528599
|
A | G | 3 | a0001c0001t0003a0001c0002t0003a0001c0004t0003 | 13 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-66T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/9 | 66 | chr10 | 13528599 | |||||
| chr10:13528673
|
A | C | 1 | a0005c0012t0014 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-140T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/9 | 140 | chr10 | 13528673 | |||||
| chr10:13528673
|
A | G | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
5_prime_UTR_variant | MODIFIER | c.-140T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/9 | 140 | chr10 | 13528673 | |||||
| chr10:13528746
|
G | A | 1 | a0001c0002t0015 | 1 | NA18962.hp2 | 5_prime_UTR_variant | MODIFIER | c.-213C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/9 | 213 | chr10 | 13528746 | |||||
| chr10:13528946
|
C | G | 1 | a0001c0004t0011 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-413G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/9 | 413 | chr10 | 13528946 | |||||
| chr10:13528952
|
G | C | 1 | a0001c0001t0010 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-419C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/9 | 419 | chr10 | 13528952 | |||||
| chr10:13528954
|
C | CGCG | 3 | a0001c0001t0005a0001c0001t0010a0001c0003t0005 | 7 | HG02258.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-424_-422dupCGC | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/9 | 422 | chr10 | 13528954 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:13441756
|
G | T | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1235-6C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13441756 | ||||||
| chr10:13441868
|
C | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(67): Show | 77 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.1235-118G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13441868 | ||||||
| chr10:13441956
|
T | C | 1 | a0001c0004t0001g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1235-206A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13441956 | ||||||
| chr10:13441961
|
T | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0207others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1235-211A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13441961 | ||||||
| chr10:13442038
|
T | C | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-288A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442038 | ||||||
| chr10:13442134
|
C | T | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-384G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442134 | ||||||
| chr10:13442200
|
G | A | 15 | a0001c0001t0001g0095a0001c0001t0001g0184a0001c0001t0001g0231others(12): Show | 15 | HG02040.hp2 HG02055.hp2 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.1235-450C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442200 | ||||||
| chr10:13442218
|
C | G | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-468G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442218 | ||||||
| chr10:13442449
|
C | T | 3 | a0001c0003t0001g0129a0002c0005t0002g0243a0002c0005t0002g0244 | 3 | HG01884.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1235-699G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442449 | ||||||
| chr10:13442453
|
T | C | 1 | a0001c0003t0001g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1235-703A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442453 | ||||||
| chr10:13442473
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1235-723C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442473 | ||||||
| chr10:13442477
|
A | G | 2 | a0001c0003t0001g0009a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1235-727T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442477 | ||||||
| chr10:13442502
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1235-752T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442502 | ||||||
| chr10:13442571
|
T | A | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-821A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442571 | ||||||
| chr10:13442582
|
C | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1235-832G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442582 | ||||||
| chr10:13442594
|
C | T | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-844G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442594 | ||||||
| chr10:13442701
|
T | G | 51 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(48): Show | 51 | HG00140.hp2 HG00408.hp2 HG01346.hp2 others(48): Show |
intron_variant | MODIFIER | c.1235-951A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442701 | ||||||
| chr10:13442879
|
C | A | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-1129G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442879 | ||||||
| chr10:13442889
|
C | A | 4 | a0001c0002t0001g0135a0001c0002t0001g0145a0001c0002t0001g0187others(1): Show | 4 | HG00558.hp1 HG02523.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1235-1139G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13442889 | ||||||
| chr10:13443043
|
T | C | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-1293A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13443043 | ||||||
| chr10:13443299
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0140a0001c0003t0001g0147 | 3 | NA18975.hp1 NA18989.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1235-1549C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13443299 | ||||||
| chr10:13443318
|
C | G | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-1568G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13443318 | ||||||
| chr10:13443357
|
T | C | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1235-1607A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13443357 | ||||||
| chr10:13443373
|
G | A | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1235-1623C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13443373 | ||||||
| chr10:13443445
|
C | T | 80 | a0001c0001t0001g0045a0001c0001t0002g0253a0001c0001t0002g0256others(77): Show | 88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1235-1695G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13443445 | ||||||
| chr10:13443569
|
A | G | 4 | a0001c0001t0006g0044a0001c0001t0006g0046a0001c0001t0006g0047others(1): Show | 4 | HG03704.hp1 NA18968.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-1819T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13443569 | ||||||
| chr10:13443634
|
G | A | 5 | a0001c0003t0001g0005a0001c0003t0001g0009a0001c0003t0001g0121others(2): Show | 8 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-1884C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13443634 | ||||||
| chr10:13444010
|
T | C | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0207others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1235-2260A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444010 | ||||||
| chr10:13444066
|
C | CT | 9 | a0001c0001t0001g0194a0001c0001t0003g0030a0001c0003t0001g0009others(6): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1235-2317dupA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444066 | ||||||
| chr10:13444156
|
G | A | 10 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1235-2406C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444156 | ||||||
| chr10:13444377
|
A | G | 10 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1235-2627T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444377 | ||||||
| chr10:13444476
|
G | T | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1235-2726C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444476 | ||||||
| chr10:13444507
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1235-2757T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444507 | ||||||
| chr10:13444692
|
A | G | 1 | a0001c0004t0001g0222 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1234+2574T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444692 | ||||||
| chr10:13444746
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(212): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1234+2520A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444746 | ||||||
| chr10:13444901
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1234+2365C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444901 | ||||||
| chr10:13444961
|
C | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0117a0001c0001t0001g0196others(3): Show | 7 | HG02486.hp2 HG02559.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1234+2305G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13444961 | ||||||
| chr10:13445007
|
CG | C | 11 | a0001c0001t0001g0045a0001c0001t0001g0075a0001c0001t0001g0076others(8): Show | 11 | HG01074.hp2 HG01261.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1234+2258delC | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13445007 | ||||||
| chr10:13445027
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1234+2239G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13445027 | ||||||
| chr10:13445215
|
A | G | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0207others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234+2051T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13445215 | ||||||
| chr10:13445451
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1234+1815T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13445451 | ||||||
| chr10:13445457
|
T | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0207others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234+1809A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13445457 | ||||||
| chr10:13445504
|
C | CCAGCTGT others(10): Show |
2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1234+1745_1234+176 others(21): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13445504 | ||||||
| chr10:13445523
|
A | G | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0207others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234+1743T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13445523 | ||||||
| chr10:13445845
|
T | C | 8 | a0001c0001t0001g0194a0001c0003t0001g0126a0001c0003t0001g0127others(5): Show | 8 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1234+1421A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13445845 | ||||||
| chr10:13445847
|
G | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(65): Show | 75 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.1234+1419C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13445847 | ||||||
| chr10:13446221
|
G | A | 1 | a0001c0003t0001g0009 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1234+1045C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446221 | ||||||
| chr10:13446239
|
G | A | 1 | a0001c0003t0001g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1234+1027C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446239 | ||||||
| chr10:13446267
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1234+999G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446267 | ||||||
| chr10:13446292
|
C | T | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1234+974G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446292 | ||||||
| chr10:13446295
|
A | G | 1 | a0001c0003t0008g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1234+971T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446295 | ||||||
| chr10:13446309
|
G | A | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234+957C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446309 | ||||||
| chr10:13446453
|
A | G | 45 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(42): Show | 45 | HG00140.hp2 HG00408.hp2 HG01346.hp2 others(42): Show |
intron_variant | MODIFIER | c.1234+813T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446453 | ||||||
| chr10:13446655
|
A | G | 1 | a0002c0005t0002g0245 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1234+611T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446655 | ||||||
| chr10:13446670
|
A | G | 1 | a0001c0004t0001g0209 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1234+596T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446670 | ||||||
| chr10:13446702
|
TAACAC | T | 39 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(36): Show | 39 | HG00140.hp2 HG00408.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.1234+559_1234+563d others(7): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446702 | ||||||
| chr10:13446741
|
A | G | 10 | a0001c0001t0001g0045a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1234+525T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446741 | ||||||
| chr10:13446787
|
C | A | 41 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(38): Show | 41 | HG00140.hp2 HG00408.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.1234+479G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13446787 | ||||||
| chr10:13447063
|
G | A | 10 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1234+203C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13447063 | ||||||
| chr10:13447148
|
T | TGCAGA | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(66): Show | 76 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.1234+113_1234+117d others(7): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13447148 | ||||||
| chr10:13447201
|
A | AT | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(119): Show | 129 | HG00140.hp2 HG00408.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.1234+64dupA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 8/8 | chr10 | 13447201 | ||||||
| chr10:13447332
|
A | G | 1 | a0001c0008t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1184-16T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447332 | ||||||
| chr10:13447536
|
C | CT | 17 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0084others(14): Show | 17 | HG00673.hp1 HG01433.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184-221dupA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447536 | ||||||
| chr10:13447536
|
CT | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(125): Show | 139 | HG00140.hp2 HG00408.hp2 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.1184-221delA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447536 | ||||||
| chr10:13447567
|
G | A | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-251C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447567 | ||||||
| chr10:13447575
|
G | A | 1 | a0001c0002t0001g0188 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1184-259C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447575 | ||||||
| chr10:13447607
|
G | C | 2 | a0001c0003t0001g0175a0001c0003t0001g0176 | 2 | NA18942.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1184-291C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447607 | ||||||
| chr10:13447692
|
C | T | 2 | a0001c0003t0001g0009a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1184-376G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447692 | ||||||
| chr10:13447700
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(65): Show | 75 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.1184-384G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447700 | ||||||
| chr10:13447704
|
T | C | 1 | a0001c0003t0001g0102 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1184-388A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447704 | ||||||
| chr10:13447776
|
C | T | 2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | HG01361.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1184-460G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447776 | ||||||
| chr10:13447839
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1184-523C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447839 | ||||||
| chr10:13447978
|
G | C | 1 | a0001c0003t0007g0270 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1184-662C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447978 | ||||||
| chr10:13447980
|
G | T | 1 | a0001c0001t0001g0220 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1184-664C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13447980 | ||||||
| chr10:13448059
|
G | C | 2 | a0001c0003t0001g0009a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1184-743C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448059 | ||||||
| chr10:13448085
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 10 | HG01081.hp1 HG01255.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1184-769A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448085 | ||||||
| chr10:13448239
|
T | C | 1 | a0001c0002t0001g0150 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1184-923A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448239 | ||||||
| chr10:13448394
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1184-1078G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448394 | ||||||
| chr10:13448451
|
A | G | 1 | a0001c0003t0001g0176 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1184-1135T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448451 | ||||||
| chr10:13448478
|
G | A | 10 | a0001c0001t0001g0045a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1184-1162C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448478 | ||||||
| chr10:13448555
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1184-1239C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448555 | ||||||
| chr10:13448563
|
C | A | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1184-1247G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448563 | ||||||
| chr10:13448692
|
G | A | 2 | a0002c0005t0002g0243a0002c0005t0002g0244 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184-1376C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448692 | ||||||
| chr10:13448742
|
G | A | 76 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(73): Show | 84 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1184-1426C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448742 | ||||||
| chr10:13448848
|
G | A | 14 | a0001c0001t0001g0095a0001c0001t0001g0184a0001c0001t0001g0231others(11): Show | 14 | HG02040.hp2 HG02055.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.1184-1532C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448848 | ||||||
| chr10:13448888
|
T | C | 1 | a0001c0003t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1184-1572A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448888 | ||||||
| chr10:13448900
|
G | A | 1 | a0001c0002t0001g0149 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1184-1584C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448900 | ||||||
| chr10:13448913
|
T | G | 2 | a0001c0003t0001g0126a0001c0003t0001g0127 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1184-1597A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448913 | ||||||
| chr10:13448928
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1184-1612C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448928 | ||||||
| chr10:13448972
|
C | CA | 53 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0097others(50): Show | 54 | HG00140.hp2 HG00408.hp2 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.1184-1657dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13448972 | ||||||
| chr10:13449076
|
T | C | 6 | a0001c0001t0001g0194a0001c0003t0002g0247a0001c0003t0005g0018others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184-1760A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13449076 | ||||||
| chr10:13449092
|
C | T | 2 | a0001c0001t0002g0256a0001c0001t0002g0267 | 2 | HG01192.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1184-1776G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13449092 | ||||||
| chr10:13449454
|
G | A | 1 | a0001c0004t0001g0205 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1184-2138C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13449454 | ||||||
| chr10:13449574
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1184-2258C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13449574 | ||||||
| chr10:13449722
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1184-2406G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13449722 | ||||||
| chr10:13449958
|
G | C | 1 | a0001c0002t0012g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1183+2581C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13449958 | ||||||
| chr10:13450087
|
A | C | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1183+2452T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450087 | ||||||
| chr10:13450172
|
A | C | 1 | a0001c0001t0002g0263 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1183+2367T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450172 | ||||||
| chr10:13450400
|
G | T | 1 | a0001c0002t0001g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1183+2139C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450400 | ||||||
| chr10:13450497
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1183+2042C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450497 | ||||||
| chr10:13450622
|
C | A | 2 | a0001c0001t0001g0195a0001c0003t0007g0272 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1183+1917G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450622 | ||||||
| chr10:13450719
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG00140.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1183+1820G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450719 | ||||||
| chr10:13450732
|
G | A | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1183+1807C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450732 | ||||||
| chr10:13450854
|
G | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(66): Show | 76 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.1183+1685C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450854 | ||||||
| chr10:13450895
|
T | C | 1 | a0001c0004t0001g0041 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1183+1644A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450895 | ||||||
| chr10:13450945
|
C | T | 2 | a0001c0003t0001g0126a0001c0003t0001g0127 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1183+1594G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450945 | ||||||
| chr10:13450963
|
G | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0207others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183+1576C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13450963 | ||||||
| chr10:13451012
|
T | C | 10 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1183+1527A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451012 | ||||||
| chr10:13451057
|
G | A | 1 | a0002c0005t0002g0245 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1183+1482C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451057 | ||||||
| chr10:13451190
|
C | CT | 9 | a0001c0001t0001g0045a0001c0001t0001g0233a0001c0001t0002g0257others(6): Show | 9 | HG00738.hp2 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183+1348dupA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451190 | ||||||
| chr10:13451221
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1183+1318C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451221 | ||||||
| chr10:13451250
|
C | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1183+1289G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451250 | ||||||
| chr10:13451362
|
A | G | 2 | a0001c0003t0001g0009a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1183+1177T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451362 | ||||||
| chr10:13451382
|
G | GGT | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0207others(5): Show | 9 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183+1155_1183+115 others(6): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451382 | ||||||
| chr10:13451602
|
G | C | 1 | a0002c0005t0002g0245 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1183+937C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451602 | ||||||
| chr10:13451670
|
T | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1183+869A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451670 | ||||||
| chr10:13451700
|
G | A | 1 | a0001c0001t0002g0256 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1183+839C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451700 | ||||||
| chr10:13451754
|
T | TC | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(217): Show | 238 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1183+784dupG | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451754 | ||||||
| chr10:13451760
|
T | C | 2 | a0001c0001t0001g0220a0001c0002t0001g0167 | 2 | HG04199.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1183+779A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451760 | ||||||
| chr10:13451760
|
T | TC | 7 | a0001c0001t0001g0054a0001c0001t0001g0067a0001c0001t0001g0074others(4): Show | 7 | HG00642.hp1 HG01261.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1183+778dupG | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451760 | ||||||
| chr10:13451761
|
C | A | 1 | a0001c0002t0012g0153 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1183+778G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451761 | ||||||
| chr10:13451761
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1183+778G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451761 | ||||||
| chr10:13451783
|
C | T | 8 | a0001c0001t0001g0225a0001c0004t0001g0015a0001c0004t0001g0016others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183+756G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451783 | ||||||
| chr10:13451807
|
T | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183+732A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451807 | ||||||
| chr10:13451815
|
T | C | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1183+724A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451815 | ||||||
| chr10:13451954
|
A | G | 1 | a0002c0005t0002g0245 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1183+585T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13451954 | ||||||
| chr10:13452075
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1183+464C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13452075 | ||||||
| chr10:13452220
|
C | T | 1 | a0001c0002t0001g0192 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1183+319G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13452220 | ||||||
| chr10:13452396
|
TAA | T | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1183+141_1183+142d others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 7/8 | chr10 | 13452396 | ||||||
| chr10:13452691
|
T | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064-33A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13452691 | ||||||
| chr10:13452738
|
GA | G | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-81delT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13452738 | ||||||
| chr10:13452787
|
C | T | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-129G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13452787 | ||||||
| chr10:13452874
|
C | T | 2 | a0001c0002t0001g0143a0001c0002t0001g0158 | 2 | NA18972.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1064-216G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13452874 | ||||||
| chr10:13452876
|
A | G | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-218T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13452876 | ||||||
| chr10:13452906
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(66): Show | 76 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.1064-248G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13452906 | ||||||
| chr10:13452979
|
T | C | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-321A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13452979 | ||||||
| chr10:13453043
|
T | C | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-385A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453043 | ||||||
| chr10:13453104
|
A | G | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-446T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453104 | ||||||
| chr10:13453133
|
G | A | 1 | a0001c0002t0001g0133 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1064-475C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453133 | ||||||
| chr10:13453176
|
C | T | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-518G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453176 | ||||||
| chr10:13453205
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1064-547C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453205 | ||||||
| chr10:13453239
|
G | A | 55 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(52): Show | 55 | HG00140.hp2 HG00408.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.1064-581C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453239 | ||||||
| chr10:13453241
|
T | C | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-583A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453241 | ||||||
| chr10:13453254
|
A | AGGC | 55 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(52): Show | 55 | HG00140.hp2 HG00408.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.1064-599_1064-597d others(5): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453254 | ||||||
| chr10:13453270
|
G | A | 1 | a0001c0003t0013g0107 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1064-612C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453270 | ||||||
| chr10:13453287
|
A | G | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-629T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453287 | ||||||
| chr10:13453416
|
G | A | 76 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(73): Show | 84 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1064-758C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453416 | ||||||
| chr10:13453437
|
T | C | 2 | a0001c0001t0003g0029a0001c0003t0001g0108 | 2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1064-779A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453437 | ||||||
| chr10:13453447
|
C | T | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-789G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453447 | ||||||
| chr10:13453589
|
A | G | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-931T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453589 | ||||||
| chr10:13453690
|
G | A | 4 | a0001c0003t0004g0110a0001c0003t0004g0111a0001c0003t0004g0113others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064-1032C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453690 | ||||||
| chr10:13453960
|
C | G | 1 | a0001c0003t0001g0009 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1064-1302G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13453960 | ||||||
| chr10:13454208
|
T | C | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-1550A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454208 | ||||||
| chr10:13454238
|
C | T | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1064-1580G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454238 | ||||||
| chr10:13454244
|
C | A | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-1586G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454244 | ||||||
| chr10:13454346
|
C | G | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1064-1688G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454346 | ||||||
| chr10:13454438
|
C | CTCAA | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-1784_1064-178 others(8): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454438 | ||||||
| chr10:13454479
|
G | A | 70 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(67): Show | 76 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1064-1821C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454479 | ||||||
| chr10:13454568
|
T | TA | 4 | a0001c0003t0004g0110a0001c0003t0004g0111a0001c0003t0004g0113others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064-1911dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454568 | ||||||
| chr10:13454710
|
A | C | 1 | a0001c0001t0002g0268 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1064-2052T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454710 | ||||||
| chr10:13454900
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1064-2242C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454900 | ||||||
| chr10:13454969
|
C | T | 2 | a0001c0003t0001g0005a0004c0010t0001g0119 | 4 | HG01891.hp2 HG02647.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064-2311G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13454969 | ||||||
| chr10:13455166
|
T | C | 1 | a0001c0002t0001g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1064-2508A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455166 | ||||||
| chr10:13455183
|
CAACAA | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064-2530_1064-252 others(9): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455183 | ||||||
| chr10:13455183
|
CAACAAAA others(3): Show |
C | 1 | a0001c0001t0002g0268 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1064-2535_1064-252 others(14): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455183 | ||||||
| chr10:13455634
|
G | A | 1 | a0001c0003t0001g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1064-2976C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455634 | ||||||
| chr10:13455653
|
G | T | 76 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(73): Show | 84 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1064-2995C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455653 | ||||||
| chr10:13455671
|
A | G | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-3013T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455671 | ||||||
| chr10:13455868
|
G | A | 6 | a0001c0001t0001g0194a0001c0003t0002g0247a0001c0003t0005g0018others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1064-3210C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455868 | ||||||
| chr10:13455903
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1064-3245G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455903 | ||||||
| chr10:13455912
|
C | T | 10 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1064-3254G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455912 | ||||||
| chr10:13455961
|
C | T | 2 | a0001c0003t0001g0009a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1064-3303G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13455961 | ||||||
| chr10:13456002
|
G | A | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-3344C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456002 | ||||||
| chr10:13456095
|
C | T | 47 | a0001c0001t0001g0039a0001c0001t0001g0087a0001c0001t0001g0088others(44): Show | 47 | HG00140.hp2 HG00408.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.1064-3437G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456095 | ||||||
| chr10:13456096
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(89): Show | 101 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.1064-3438C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456096 | ||||||
| chr10:13456264
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1064-3606A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456264 | ||||||
| chr10:13456266
|
T | C | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-3608A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456266 | ||||||
| chr10:13456305
|
G | A | 3 | a0001c0003t0001g0129a0002c0005t0002g0243a0002c0005t0002g0244 | 3 | HG01884.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1064-3647C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456305 | ||||||
| chr10:13456371
|
A | G | 77 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(74): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1064-3713T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456371 | ||||||
| chr10:13456418
|
A | G | 78 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(75): Show | 86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1064-3760T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456418 | ||||||
| chr10:13456569
|
C | T | 28 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(25): Show | 28 | HG02040.hp2 HG02055.hp2 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.1064-3911G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456569 | ||||||
| chr10:13456602
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1064-3944G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456602 | ||||||
| chr10:13456651
|
C | T | 1 | a0001c0003t0001g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1064-3993G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456651 | ||||||
| chr10:13456655
|
T | C | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1064-3997A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13456655 | ||||||
| chr10:13457205
|
G | A | 2 | a0001c0003t0008g0248a0001c0003t0008g0251 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1064-4547C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13457205 | ||||||
| chr10:13457244
|
C | T | 1 | a0001c0003t0002g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1064-4586G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13457244 | ||||||
| chr10:13457253
|
C | A | 76 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(73): Show | 84 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1064-4595G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13457253 | ||||||
| chr10:13457395
|
T | C | 78 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(75): Show | 86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1064-4737A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13457395 | ||||||
| chr10:13457401
|
C | G | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1064-4743G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13457401 | ||||||
| chr10:13457547
|
A | T | 47 | a0001c0001t0001g0039a0001c0001t0001g0087a0001c0001t0001g0088others(44): Show | 47 | HG00140.hp2 HG00408.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.1064-4889T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13457547 | ||||||
| chr10:13457637
|
T | C | 1 | a0001c0007t0002g0242 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1064-4979A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13457637 | ||||||
| chr10:13457819
|
A | G | 1 | a0001c0004t0001g0209 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1064-5161T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13457819 | ||||||
| chr10:13457935
|
C | T | 6 | a0001c0001t0001g0194a0001c0003t0002g0247a0001c0003t0005g0018others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1064-5277G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13457935 | ||||||
| chr10:13458098
|
T | C | 1 | a0001c0001t0002g0256 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1064-5440A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13458098 | ||||||
| chr10:13458295
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1064-5637G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13458295 | ||||||
| chr10:13458616
|
T | C | 28 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(25): Show | 28 | HG02040.hp2 HG02055.hp2 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.1064-5958A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13458616 | ||||||
| chr10:13458749
|
A | G | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1064-6091T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13458749 | ||||||
| chr10:13458881
|
G | A | 1 | a0001c0004t0001g0237 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1064-6223C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13458881 | ||||||
| chr10:13458960
|
G | C | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-6302C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13458960 | ||||||
| chr10:13459002
|
G | A | 12 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 12 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1064-6344C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459002 | ||||||
| chr10:13459097
|
C | A | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-6439G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459097 | ||||||
| chr10:13459202
|
T | C | 157 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0087others(154): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1064-6544A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459202 | ||||||
| chr10:13459289
|
G | T | 42 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(39): Show | 42 | HG00140.hp2 HG00408.hp2 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.1064-6631C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459289 | ||||||
| chr10:13459415
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1064-6757G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459415 | ||||||
| chr10:13459422
|
C | T | 6 | a0001c0003t0001g0112a0001c0003t0001g0122a0001c0003t0001g0123others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1064-6764G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459422 | ||||||
| chr10:13459685
|
A | C | 1 | a0001c0002t0001g0181 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1064-7027T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459685 | ||||||
| chr10:13459699
|
A | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0226 | 2 | HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1064-7041T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459699 | ||||||
| chr10:13459787
|
T | C | 2 | a0001c0004t0001g0222a0001c0004t0001g0223 | 2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1064-7129A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459787 | ||||||
| chr10:13459822
|
CA | C | 11 | a0001c0002t0001g0010a0001c0002t0001g0146a0001c0002t0001g0150others(8): Show | 12 | HG00558.hp2 HG00642.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1064-7165delT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459822 | ||||||
| chr10:13459870
|
C | T | 2 | a0001c0001t0001g0118a0005c0012t0014g0273 | 2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1064-7212G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459870 | ||||||
| chr10:13459871
|
G | A | 2 | a0001c0003t0001g0009a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1064-7213C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13459871 | ||||||
| chr10:13460070
|
A | C | 87 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0087others(84): Show | 89 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.1064-7412T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460070 | ||||||
| chr10:13460108
|
C | T | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1064-7450G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460108 | ||||||
| chr10:13460167
|
G | A | 35 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(32): Show | 37 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1064-7509C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460167 | ||||||
| chr10:13460177
|
A | G | 35 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(32): Show | 37 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1064-7519T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460177 | ||||||
| chr10:13460180
|
A | G | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0207others(2): Show | 5 | HG01243.hp2 HG01884.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-7522T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460180 | ||||||
| chr10:13460206
|
G | A | 10 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1064-7548C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460206 | ||||||
| chr10:13460357
|
T | C | 35 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(32): Show | 37 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1064-7699A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460357 | ||||||
| chr10:13460400
|
G | C | 47 | a0001c0001t0001g0039a0001c0001t0001g0087a0001c0001t0001g0088others(44): Show | 47 | HG00140.hp2 HG00408.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.1064-7742C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460400 | ||||||
| chr10:13460508
|
T | A | 35 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(32): Show | 37 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1064-7850A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460508 | ||||||
| chr10:13460707
|
A | C | 28 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(25): Show | 28 | HG02040.hp2 HG02055.hp2 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.1064-8049T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13460707 | ||||||
| chr10:13461080
|
G | T | 1 | a0001c0003t0001g0121 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1064-8422C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461080 | ||||||
| chr10:13461088
|
A | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0049a0001c0001t0001g0053others(18): Show | 23 | HG00140.hp1 HG00280.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1064-8430T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461088 | ||||||
| chr10:13461371
|
C | T | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1064-8713G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461371 | ||||||
| chr10:13461500
|
C | T | 48 | a0001c0001t0001g0039a0001c0001t0001g0087a0001c0001t0001g0088others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1064-8842G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461500 | ||||||
| chr10:13461561
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1064-8903G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461561 | ||||||
| chr10:13461621
|
T | C | 14 | a0001c0001t0001g0095a0001c0001t0001g0184a0001c0001t0001g0231others(11): Show | 14 | HG02040.hp2 HG02055.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064-8963A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461621 | ||||||
| chr10:13461648
|
G | T | 1 | a0001c0001t0006g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1064-8990C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461648 | ||||||
| chr10:13461660
|
G | A | 2 | a0001c0001t0003g0029a0001c0003t0001g0108 | 2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1064-9002C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461660 | ||||||
| chr10:13461732
|
T | TA | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(136): Show | 155 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1064-9075dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461732 | ||||||
| chr10:13461734
|
A | G | 51 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0087others(48): Show | 51 | HG00140.hp2 HG00408.hp2 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.1064-9076T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461734 | ||||||
| chr10:13461945
|
C | A | 47 | a0001c0001t0001g0039a0001c0001t0001g0087a0001c0001t0001g0088others(44): Show | 47 | HG00140.hp2 HG00408.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.1064-9287G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461945 | ||||||
| chr10:13461989
|
A | G | 1 | a0001c0003t0002g0249 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1064-9331T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13461989 | ||||||
| chr10:13462245
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1064-9587C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13462245 | ||||||
| chr10:13462257
|
C | CA | 21 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(18): Show | 21 | HG02055.hp2 HG02602.hp2 HG02735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1064-9600dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13462257 | ||||||
| chr10:13462371
|
A | G | 2 | a0001c0004t0001g0200a0001c0004t0001g0209 | 2 | HG00673.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1064-9713T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13462371 | ||||||
| chr10:13462399
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(215): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1064-9741A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13462399 | ||||||
| chr10:13462471
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(149): Show | 166 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1064-9813T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13462471 | ||||||
| chr10:13462600
|
T | C | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-9942A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13462600 | ||||||
| chr10:13462706
|
T | C | 86 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(83): Show | 91 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.1064-10048A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13462706 | ||||||
| chr10:13462761
|
A | C | 2 | a0001c0004t0001g0200a0001c0004t0001g0209 | 2 | HG00673.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1064-10103T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13462761 | ||||||
| chr10:13462779
|
G | A | 1 | a0001c0002t0001g0154 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1064-10121C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13462779 | ||||||
| chr10:13463194
|
TA | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(218): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1064-10537delT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13463194 | ||||||
| chr10:13463382
|
A | G | 1 | a0001c0001t0003g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1064-10724T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13463382 | ||||||
| chr10:13463421
|
A | G | 4 | a0001c0003t0001g0005a0001c0003t0001g0121a0001c0003t0001g0128others(1): Show | 6 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1064-10763T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13463421 | ||||||
| chr10:13463496
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1064-10838C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13463496 | ||||||
| chr10:13463751
|
C | T | 2 | a0001c0004t0001g0234a0001c0004t0001g0237 | 2 | NA18989.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1064-11093G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13463751 | ||||||
| chr10:13464107
|
T | C | 2 | a0001c0003t0001g0126a0001c0003t0001g0127 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1064-11449A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13464107 | ||||||
| chr10:13464219
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1064-11561G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13464219 | ||||||
| chr10:13464220
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1064-11562T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13464220 | ||||||
| chr10:13464291
|
A | G | 1 | a0001c0001t0002g0264 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1064-11633T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13464291 | ||||||
| chr10:13464414
|
C | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(218): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1064-11756G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13464414 | ||||||
| chr10:13464516
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(218): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1064-11858G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13464516 | ||||||
| chr10:13464537
|
G | A | 1 | a0001c0007t0002g0242 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1064-11879C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13464537 | ||||||
| chr10:13464758
|
G | C | 1 | a0001c0003t0001g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1064-12100C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13464758 | ||||||
| chr10:13464831
|
T | C | 1 | a0001c0002t0001g0169 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1064-12173A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13464831 | ||||||
| chr10:13465019
|
T | G | 2 | a0001c0004t0001g0200a0001c0004t0001g0209 | 2 | HG00673.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1064-12361A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465019 | ||||||
| chr10:13465033
|
G | C | 33 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(30): Show | 36 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1064-12375C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465033 | ||||||
| chr10:13465123
|
T | C | 1 | a0001c0008t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1064-12465A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465123 | ||||||
| chr10:13465329
|
T | A | 3 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048 | 3 | NA18968.hp2 NA18997.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1064-12671A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465329 | ||||||
| chr10:13465384
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(158): Show | 177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1064-12726A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465384 | ||||||
| chr10:13465429
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1064-12771C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465429 | ||||||
| chr10:13465432
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(127): Show | 144 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1064-12774G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465432 | ||||||
| chr10:13465452
|
T | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064-12794A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465452 | ||||||
| chr10:13465532
|
G | A | 1 | a0001c0003t0002g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1064-12874C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465532 | ||||||
| chr10:13465550
|
G | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 10 | HG01081.hp1 HG01255.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1064-12892C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465550 | ||||||
| chr10:13465750
|
C | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 6 | HG00735.hp2 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1064-13092G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465750 | ||||||
| chr10:13465878
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1064-13220G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465878 | ||||||
| chr10:13465884
|
CGT | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(215): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1064-13228_1064-13 others(8): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13465884 | ||||||
| chr10:13466136
|
T | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(38): Show | 48 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1064-13478A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466136 | ||||||
| chr10:13466156
|
C | T | 12 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(9): Show | 12 | HG02055.hp2 HG02602.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1064-13498G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466156 | ||||||
| chr10:13466228
|
A | AT | 47 | a0001c0001t0001g0039a0001c0001t0001g0083a0001c0001t0001g0089others(44): Show | 47 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1064-13571dupA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466228 | ||||||
| chr10:13466295
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1064-13637A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466295 | ||||||
| chr10:13466357
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1064-13699A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466357 | ||||||
| chr10:13466380
|
C | T | 2 | a0001c0003t0001g0126a0001c0003t0001g0127 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1064-13722G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466380 | ||||||
| chr10:13466436
|
G | T | 1 | a0001c0002t0001g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1064-13778C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466436 | ||||||
| chr10:13466478
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1064-13820C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466478 | ||||||
| chr10:13466558
|
CA | C | 99 | a0001c0001t0001g0045a0001c0001t0001g0095a0001c0001t0001g0096others(96): Show | 106 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1064-13901delT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466558 | ||||||
| chr10:13466558
|
CAA | C | 10 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(7): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1064-13902_1064-13 others(8): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466558 | ||||||
| chr10:13466707
|
T | C | 20 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(17): Show | 20 | HG02055.hp2 HG02602.hp2 HG02735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1064-14049A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466707 | ||||||
| chr10:13466776
|
G | T | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-14118C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466776 | ||||||
| chr10:13466896
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1063+14003G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466896 | ||||||
| chr10:13466961
|
T | G | 68 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(65): Show | 70 | HG00140.hp2 HG00673.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.1063+13938A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13466961 | ||||||
| chr10:13467005
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1063+13894C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467005 | ||||||
| chr10:13467016
|
G | A | 2 | a0001c0001t0002g0240a0001c0001t0002g0241 | 2 | NA19002.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1063+13883C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467016 | ||||||
| chr10:13467079
|
G | A | 24 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(21): Show | 24 | HG02055.hp2 HG02572.hp2 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.1063+13820C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467079 | ||||||
| chr10:13467083
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(176): Show | 193 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1063+13816C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467083 | ||||||
| chr10:13467216
|
A | G | 11 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(8): Show | 13 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1063+13683T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467216 | ||||||
| chr10:13467219
|
C | T | 3 | a0001c0002t0001g0159a0001c0002t0001g0160a0001c0002t0001g0161 | 3 | HG00558.hp2 HG02129.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1063+13680G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467219 | ||||||
| chr10:13467286
|
G | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+13613C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467286 | ||||||
| chr10:13467447
|
A | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0049others(24): Show | 30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.1063+13452T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467447 | ||||||
| chr10:13467517
|
A | G | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+13382T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467517 | ||||||
| chr10:13467620
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1063+13279A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467620 | ||||||
| chr10:13467708
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1063+13191A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467708 | ||||||
| chr10:13467884
|
T | G | 1 | a0001c0002t0001g0189 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1063+13015A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467884 | ||||||
| chr10:13467987
|
T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(189): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1063+12912A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13467987 | ||||||
| chr10:13468030
|
C | T | 12 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(9): Show | 12 | HG02055.hp2 HG02602.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063+12869G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468030 | ||||||
| chr10:13468060
|
G | A | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+12839C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468060 | ||||||
| chr10:13468118
|
T | C | 43 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(40): Show | 43 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1063+12781A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468118 | ||||||
| chr10:13468122
|
C | T | 17 | a0001c0001t0001g0039a0001c0001t0001g0197a0001c0001t0001g0198others(14): Show | 17 | HG00140.hp2 HG00408.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.1063+12777G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468122 | ||||||
| chr10:13468146
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1063+12753G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468146 | ||||||
| chr10:13468347
|
G | C | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1063+12552C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468347 | ||||||
| chr10:13468402
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1063+12497C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468402 | ||||||
| chr10:13468460
|
C | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+12439G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468460 | ||||||
| chr10:13468746
|
A | G | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+12153T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468746 | ||||||
| chr10:13468749
|
G | C | 34 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0095others(31): Show | 36 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1063+12150C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468749 | ||||||
| chr10:13468760
|
G | A | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+12139C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468760 | ||||||
| chr10:13468910
|
T | C | 23 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(20): Show | 23 | HG02055.hp2 HG02602.hp2 HG02735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1063+11989A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13468910 | ||||||
| chr10:13469130
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(128): Show | 145 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1063+11769C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469130 | ||||||
| chr10:13469139
|
A | G | 1 | a0001c0002t0001g0182 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1063+11760T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469139 | ||||||
| chr10:13469256
|
C | G | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+11643G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469256 | ||||||
| chr10:13469365
|
CA | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1063+11533delT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469365 | ||||||
| chr10:13469456
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0214a0001c0001t0001g0226 | 3 | HG01258.hp1 HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1063+11443C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469456 | ||||||
| chr10:13469579
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(185): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1063+11320A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469579 | ||||||
| chr10:13469601
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1063+11298A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469601 | ||||||
| chr10:13469604
|
G | A | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+11295C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469604 | ||||||
| chr10:13469643
|
A | G | 43 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(40): Show | 43 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1063+11256T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469643 | ||||||
| chr10:13469675
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0073a0001c0001t0001g0074others(19): Show | 24 | HG00544.hp2 HG00609.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1063+11224G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469675 | ||||||
| chr10:13469704
|
C | T | 1 | a0002c0005t0002g0245 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1063+11195G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469704 | ||||||
| chr10:13469757
|
G | A | 3 | a0001c0001t0001g0118a0001c0003t0005g0017a0005c0012t0014g0273 | 3 | HG03041.hp1 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1063+11142C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469757 | ||||||
| chr10:13469768
|
C | A | 1 | a0001c0002t0001g0192 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1063+11131G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469768 | ||||||
| chr10:13469797
|
GT | G | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+11101delA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469797 | ||||||
| chr10:13469986
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(140): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1063+10913A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13469986 | ||||||
| chr10:13470064
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1063+10835C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13470064 | ||||||
| chr10:13470223
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(142): Show | 161 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1063+10676A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13470223 | ||||||
| chr10:13470326
|
C | T | 5 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0215others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063+10573G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13470326 | ||||||
| chr10:13470428
|
C | CT | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+10470_1063+10 others(7): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13470428 | ||||||
| chr10:13470431
|
T | TGTGACAA others(3): Show |
4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+10467_1063+10 others(16): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13470431 | ||||||
| chr10:13470485
|
G | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063+10414C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13470485 | ||||||
| chr10:13470670
|
C | T | 43 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(40): Show | 43 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1063+10229G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13470670 | ||||||
| chr10:13470769
|
C | G | 1 | a0001c0003t0008g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063+10130G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13470769 | ||||||
| chr10:13470909
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0217a0001c0001t0001g0219others(1): Show | 4 | HG00621.hp2 HG00673.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063+9990C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13470909 | ||||||
| chr10:13471042
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1063+9857T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471042 | ||||||
| chr10:13471089
|
C | T | 14 | a0001c0001t0001g0171a0001c0001t0002g0252a0001c0001t0002g0254others(11): Show | 14 | HG01192.hp2 HG01346.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1063+9810G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471089 | ||||||
| chr10:13471114
|
T | G | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+9785A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471114 | ||||||
| chr10:13471154
|
T | C | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1063+9745A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471154 | ||||||
| chr10:13471300
|
A | G | 1 | a0001c0003t0005g0020 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1063+9599T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471300 | ||||||
| chr10:13471368
|
C | T | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1063+9531G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471368 | ||||||
| chr10:13471418
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0006g0046 | 2 | HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1063+9481G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471418 | ||||||
| chr10:13471429
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1063+9470T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471429 | ||||||
| chr10:13471430
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(145): Show | 164 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1063+9469T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471430 | ||||||
| chr10:13471715
|
G | A | 43 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(40): Show | 43 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1063+9184C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471715 | ||||||
| chr10:13471950
|
TCACTGTT others(55): Show |
T | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+8887_1063+894 others(66): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13471950 | ||||||
| chr10:13472056
|
C | T | 1 | a0001c0002t0001g0165 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1063+8843G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472056 | ||||||
| chr10:13472093
|
C | T | 1 | a0001c0004t0001g0205 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1063+8806G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472093 | ||||||
| chr10:13472094
|
G | A | 3 | a0001c0003t0001g0129a0002c0005t0002g0243a0002c0005t0002g0244 | 3 | HG01884.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1063+8805C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472094 | ||||||
| chr10:13472122
|
G | A | 3 | a0001c0001t0001g0118a0001c0003t0005g0017a0005c0012t0014g0273 | 3 | HG03041.hp1 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1063+8777C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472122 | ||||||
| chr10:13472181
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(140): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1063+8718T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472181 | ||||||
| chr10:13472318
|
G | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+8581C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472318 | ||||||
| chr10:13472353
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(212): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1063+8546A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472353 | ||||||
| chr10:13472509
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(220): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1063+8390A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472509 | ||||||
| chr10:13472556
|
C | CGATATCC others(24): Show |
1 | a0001c0002t0001g0150 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1063+8312_1063+834 others(35): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472556 | ||||||
| chr10:13472564
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1063+8335C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472564 | ||||||
| chr10:13472588
|
G | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+8311C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472588 | ||||||
| chr10:13472698
|
C | G | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1063+8201G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472698 | ||||||
| chr10:13472809
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1063+8090G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472809 | ||||||
| chr10:13472816
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1063+8083C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472816 | ||||||
| chr10:13472841
|
G | A | 1 | a0001c0003t0001g0128 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1063+8058C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472841 | ||||||
| chr10:13472890
|
G | A | 1 | a0001c0001t0002g0258 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1063+8009C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472890 | ||||||
| chr10:13472982
|
C | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+7917G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13472982 | ||||||
| chr10:13473046
|
G | T | 1 | a0001c0004t0001g0041 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1063+7853C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473046 | ||||||
| chr10:13473094
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 138 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1063+7805G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473094 | ||||||
| chr10:13473117
|
A | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(143): Show | 162 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1063+7782T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473117 | ||||||
| chr10:13473248
|
C | T | 4 | a0001c0003t0001g0129a0001c0004t0001g0223a0002c0005t0002g0243others(1): Show | 4 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+7651G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473248 | ||||||
| chr10:13473326
|
A | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(187): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1063+7573T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473326 | ||||||
| chr10:13473335
|
G | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 138 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1063+7564C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473335 | ||||||
| chr10:13473370
|
C | T | 1 | a0001c0003t0001g0148 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1063+7529G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473370 | ||||||
| chr10:13473411
|
C | T | 6 | a0001c0001t0001g0194a0001c0003t0002g0247a0001c0003t0005g0018others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063+7488G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473411 | ||||||
| chr10:13473427
|
G | A | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0005others(14): Show | 19 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1063+7472C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473427 | ||||||
| chr10:13473434
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1063+7465G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473434 | ||||||
| chr10:13473562
|
T | TAGACTC | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(187): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1063+7336_1063+733 others(10): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473562 | ||||||
| chr10:13473592
|
C | T | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+7307G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473592 | ||||||
| chr10:13473628
|
C | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+7271G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473628 | ||||||
| chr10:13473679
|
G | A | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1063+7220C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473679 | ||||||
| chr10:13473907
|
G | A | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+6992C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473907 | ||||||
| chr10:13473916
|
G | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(211): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1063+6983C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473916 | ||||||
| chr10:13473942
|
T | C | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1063+6957A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473942 | ||||||
| chr10:13473975
|
G | C | 2 | a0001c0002t0001g0166a0001c0002t0001g0170 | 2 | HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1063+6924C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13473975 | ||||||
| chr10:13474096
|
C | G | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+6803G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474096 | ||||||
| chr10:13474103
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1063+6796A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474103 | ||||||
| chr10:13474201
|
G | C | 1 | a0001c0004t0001g0041 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1063+6698C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474201 | ||||||
| chr10:13474228
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1063+6671G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474228 | ||||||
| chr10:13474322
|
G | A | 17 | a0001c0001t0001g0039a0001c0001t0001g0197a0001c0001t0001g0198others(14): Show | 17 | HG00140.hp2 HG00408.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.1063+6577C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474322 | ||||||
| chr10:13474336
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1063+6563C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474336 | ||||||
| chr10:13474347
|
G | A | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+6552C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474347 | ||||||
| chr10:13474425
|
T | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1063+6474A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474425 | ||||||
| chr10:13474426
|
C | T | 69 | a0001c0001t0001g0045a0001c0001t0006g0046a0001c0002t0001g0002others(66): Show | 75 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1063+6473G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474426 | ||||||
| chr10:13474469
|
C | T | 49 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(46): Show | 49 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1063+6430G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474469 | ||||||
| chr10:13474476
|
A | G | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+6423T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474476 | ||||||
| chr10:13474487
|
C | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02630.hp1 HG02809.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+6412G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474487 | ||||||
| chr10:13474492
|
C | CCGATACC others(23): Show |
1 | a0001c0004t0001g0205 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1063+6377_1063+640 others(34): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474492 | ||||||
| chr10:13474493
|
CGATACCC others(53): Show |
C | 1 | a0001c0003t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1063+6346_1063+640 others(64): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474493 | ||||||
| chr10:13474518
|
C | T | 19 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(16): Show | 19 | HG02572.hp2 HG02602.hp2 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1063+6381G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474518 | ||||||
| chr10:13474524
|
G | A | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1063+6375C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474524 | ||||||
| chr10:13474553
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1063+6346A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474553 | ||||||
| chr10:13474567
|
G | A | 2 | a0001c0006t0004g0105a0001c0006t0004g0106 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1063+6332C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474567 | ||||||
| chr10:13474621
|
G | A | 6 | a0001c0003t0001g0112a0001c0003t0001g0122a0001c0003t0001g0123others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063+6278C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474621 | ||||||
| chr10:13474625
|
T | C | 1 | a0001c0003t0004g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1063+6274A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474625 | ||||||
| chr10:13474627
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(118): Show | 135 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1063+6272C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474627 | ||||||
| chr10:13474669
|
C | G | 1 | a0001c0003t0004g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1063+6230G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474669 | ||||||
| chr10:13474758
|
T | C | 5 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | NA18942.hp2 NA18968.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+6141A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474758 | ||||||
| chr10:13474815
|
A | C | 1 | a0001c0003t0001g0128 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1063+6084T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474815 | ||||||
| chr10:13474923
|
G | A | 1 | a0001c0004t0001g0205 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1063+5976C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474923 | ||||||
| chr10:13474938
|
T | G | 44 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(41): Show | 44 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1063+5961A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13474938 | ||||||
| chr10:13475302
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(188): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1063+5597A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13475302 | ||||||
| chr10:13475374
|
C | A | 1 | a0001c0002t0001g0160 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1063+5525G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13475374 | ||||||
| chr10:13475380
|
A | G | 44 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0001t0001g0093others(41): Show | 44 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1063+5519T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13475380 | ||||||
| chr10:13475655
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1063+5244G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13475655 | ||||||
| chr10:13475673
|
C | T | 6 | a0001c0003t0001g0112a0001c0003t0001g0122a0001c0003t0001g0123others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063+5226G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13475673 | ||||||
| chr10:13475707
|
C | CA | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(188): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1063+5191dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13475707 | ||||||
| chr10:13475817
|
G | A | 24 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(21): Show | 24 | HG02572.hp2 HG02602.hp2 HG02735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1063+5082C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13475817 | ||||||
| chr10:13475919
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1063+4980G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13475919 | ||||||
| chr10:13475978
|
G | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(120): Show | 137 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1063+4921C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13475978 | ||||||
| chr10:13476048
|
A | C | 3 | a0001c0001t0001g0118a0001c0003t0005g0017a0005c0012t0014g0273 | 3 | HG03041.hp1 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1063+4851T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13476048 | ||||||
| chr10:13476107
|
T | A | 3 | a0001c0003t0001g0005a0001c0003t0001g0121a0004c0010t0001g0119 | 5 | HG01891.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+4792A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13476107 | ||||||
| chr10:13476273
|
C | T | 12 | a0001c0002t0001g0002a0001c0002t0001g0103a0001c0002t0001g0134others(9): Show | 15 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063+4626G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13476273 | ||||||
| chr10:13476530
|
CG | C | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1063+4368delC | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13476530 | ||||||
| chr10:13476662
|
G | A | 1 | a0001c0003t0013g0107 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1063+4237C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13476662 | ||||||
| chr10:13476741
|
C | T | 1 | a0001c0003t0001g0009 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1063+4158G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13476741 | ||||||
| chr10:13476943
|
A | C | 1 | a0001c0001t0001g0210 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1063+3956T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13476943 | ||||||
| chr10:13477253
|
T | C | 2 | a0001c0004t0001g0200a0001c0004t0001g0209 | 2 | HG00673.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1063+3646A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13477253 | ||||||
| chr10:13477514
|
C | A | 66 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0087others(63): Show | 67 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.1063+3385G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13477514 | ||||||
| chr10:13477552
|
G | A | 3 | a0001c0001t0006g0044a0001c0001t0006g0047a0001c0001t0006g0048 | 3 | NA18968.hp2 NA18997.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1063+3347C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13477552 | ||||||
| chr10:13477743
|
G | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(139): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1063+3156C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13477743 | ||||||
| chr10:13478045
|
G | A | 1 | a0001c0002t0001g0169 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1063+2854C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478045 | ||||||
| chr10:13478119
|
T | G | 1 | a0001c0003t0001g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1063+2780A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478119 | ||||||
| chr10:13478163
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 139 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1063+2736G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478163 | ||||||
| chr10:13478265
|
A | G | 1 | a0001c0002t0001g0192 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1063+2634T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478265 | ||||||
| chr10:13478466
|
C | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(139): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1063+2433G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478466 | ||||||
| chr10:13478500
|
G | C | 1 | a0001c0008t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1063+2399C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478500 | ||||||
| chr10:13478542
|
C | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1063+2357G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478542 | ||||||
| chr10:13478591
|
TATA | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(139): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1063+2305_1063+230 others(7): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478591 | ||||||
| chr10:13478613
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(139): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1063+2286C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478613 | ||||||
| chr10:13478724
|
T | C | 2 | a0001c0001t0001g0014a0001c0004t0001g0203 | 3 | HG00099.hp2 HG00639.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1063+2175A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478724 | ||||||
| chr10:13478728
|
TAAACACT others(8): Show |
T | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+2156_1063+217 others(19): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478728 | ||||||
| chr10:13478790
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1063+2109A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478790 | ||||||
| chr10:13478850
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1063+2049T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478850 | ||||||
| chr10:13478900
|
T | C | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+1999A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13478900 | ||||||
| chr10:13479005
|
A | G | 1 | a0001c0003t0001g0128 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1063+1894T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479005 | ||||||
| chr10:13479006
|
CT | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(140): Show | 160 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1063+1892delA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479006 | ||||||
| chr10:13479007
|
T | A | 1 | a0001c0001t0006g0048 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1063+1892A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479007 | ||||||
| chr10:13479093
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(114): Show | 130 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1063+1806C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479093 | ||||||
| chr10:13479095
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(121): Show | 139 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1063+1804G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479095 | ||||||
| chr10:13479169
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0226 | 2 | HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1063+1730C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479169 | ||||||
| chr10:13479234
|
G | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(139): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1063+1665C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479234 | ||||||
| chr10:13479301
|
G | A | 2 | a0001c0003t0005g0020a0001c0003t0005g0021 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1063+1598C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479301 | ||||||
| chr10:13479331
|
T | C | 2 | a0001c0003t0004g0113a0001c0003t0004g0114 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1063+1568A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479331 | ||||||
| chr10:13479702
|
A | C | 1 | a0001c0003t0001g0164 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1063+1197T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479702 | ||||||
| chr10:13479743
|
C | A | 1 | a0001c0003t0001g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1063+1156G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479743 | ||||||
| chr10:13479765
|
A | C | 2 | a0001c0001t0001g0014a0001c0004t0001g0203 | 3 | HG00099.hp2 HG00639.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1063+1134T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479765 | ||||||
| chr10:13479770
|
T | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+1129A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479770 | ||||||
| chr10:13479808
|
T | TGTCCTTC | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(115): Show | 131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1063+1084_1063+109 others(11): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479808 | ||||||
| chr10:13479854
|
A | G | 49 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0089others(46): Show | 50 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1063+1045T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479854 | ||||||
| chr10:13479916
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(142): Show | 162 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1063+983G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13479916 | ||||||
| chr10:13480094
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0221 | 2 | HG00408.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1063+805A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13480094 | ||||||
| chr10:13480237
|
A | G | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1063+662T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13480237 | ||||||
| chr10:13480330
|
G | A | 3 | a0001c0002t0001g0173a0001c0002t0001g0189a0001c0002t0001g0191 | 3 | HG02135.hp1 NA18967.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1063+569C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13480330 | ||||||
| chr10:13480469
|
C | T | 1 | a0001c0002t0001g0134 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1063+430G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13480469 | ||||||
| chr10:13480515
|
C | CT | 9 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0028others(6): Show | 9 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.1063+383dupA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13480515 | ||||||
| chr10:13480595
|
C | CTTAG | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(144): Show | 164 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1063+300_1063+303d others(6): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13480595 | ||||||
| chr10:13480631
|
A | G | 1 | a0001c0003t0001g0138 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1063+268T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13480631 | ||||||
| chr10:13480661
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(144): Show | 164 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1063+238C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13480661 | ||||||
| chr10:13480812
|
T | A | 2 | a0001c0003t0001g0126a0001c0003t0001g0127 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1063+87A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 6/8 | chr10 | 13480812 | ||||||
| chr10:13481378
|
C | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(145): Show | 165 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.838-254G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13481378 | ||||||
| chr10:13481457
|
ACAAAGGA others(9): Show |
A | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.838-349_838-334del others(16): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13481457 | ||||||
| chr10:13481541
|
C | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(141): Show | 161 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.838-417G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13481541 | ||||||
| chr10:13481591
|
T | C | 2 | a0001c0003t0001g0138a0001c0003t0001g0140 | 2 | NA18989.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.838-467A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13481591 | ||||||
| chr10:13481612
|
C | T | 3 | a0001c0003t0001g0129a0002c0005t0002g0243a0002c0005t0002g0244 | 3 | HG01884.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.838-488G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13481612 | ||||||
| chr10:13481763
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(218): Show | 239 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.838-639T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13481763 | ||||||
| chr10:13481808
|
T | G | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.838-684A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13481808 | ||||||
| chr10:13481864
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(130): Show | 148 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.838-740C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13481864 | ||||||
| chr10:13481937
|
C | T | 73 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(70): Show | 79 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.838-813G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13481937 | ||||||
| chr10:13482213
|
T | C | 1 | a0001c0002t0001g0143 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.838-1089A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482213 | ||||||
| chr10:13482219
|
A | G | 6 | a0001c0003t0001g0112a0001c0003t0001g0122a0001c0003t0001g0123others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-1095T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482219 | ||||||
| chr10:13482279
|
G | A | 4 | a0001c0003t0004g0110a0001c0003t0004g0111a0001c0003t0004g0113others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-1155C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482279 | ||||||
| chr10:13482475
|
A | C | 1 | a0001c0004t0001g0224 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.838-1351T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482475 | ||||||
| chr10:13482498
|
T | C | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.838-1374A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482498 | ||||||
| chr10:13482617
|
G | C | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.838-1493C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482617 | ||||||
| chr10:13482642
|
C | T | 1 | a0001c0002t0001g0145 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.838-1518G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482642 | ||||||
| chr10:13482672
|
C | G | 1 | a0001c0004t0001g0209 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.838-1548G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482672 | ||||||
| chr10:13482763
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.838-1639A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482763 | ||||||
| chr10:13482831
|
A | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.838-1707T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482831 | ||||||
| chr10:13482983
|
G | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0001g0120others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-1859C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13482983 | ||||||
| chr10:13483061
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.838-1937T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13483061 | ||||||
| chr10:13483170
|
T | C | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.838-2046A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13483170 | ||||||
| chr10:13483175
|
A | G | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.838-2051T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13483175 | ||||||
| chr10:13483258
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.838-2134T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13483258 | ||||||
| chr10:13483487
|
A | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.838-2363T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13483487 | ||||||
| chr10:13483517
|
T | C | 1 | a0001c0001t0002g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.838-2393A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13483517 | ||||||
| chr10:13483746
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.838-2622T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13483746 | ||||||
| chr10:13483847
|
T | C | 2 | a0002c0005t0002g0243a0002c0005t0002g0244 | 2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.838-2723A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13483847 | ||||||
| chr10:13483890
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.838-2766C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13483890 | ||||||
| chr10:13484000
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(145): Show | 165 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.838-2876A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484000 | ||||||
| chr10:13484023
|
C | A | 7 | a0001c0001t0001g0194a0001c0003t0002g0247a0001c0003t0005g0017others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.838-2899G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484023 | ||||||
| chr10:13484086
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0006g0046 | 2 | HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.838-2962G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484086 | ||||||
| chr10:13484147
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.838-3023C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484147 | ||||||
| chr10:13484219
|
A | T | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.838-3095T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484219 | ||||||
| chr10:13484243
|
G | A | 6 | a0001c0003t0001g0112a0001c0003t0001g0122a0001c0003t0001g0123others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-3119C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484243 | ||||||
| chr10:13484521
|
T | A | 21 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(18): Show | 21 | HG02572.hp2 HG02602.hp2 HG02735.hp2 others(18): Show |
intron_variant | MODIFIER | c.838-3397A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484521 | ||||||
| chr10:13484558
|
C | A | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.838-3434G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484558 | ||||||
| chr10:13484617
|
T | C | 47 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0089others(44): Show | 48 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.838-3493A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484617 | ||||||
| chr10:13484637
|
G | C | 2 | a0001c0004t0001g0222a0001c0004t0001g0223 | 2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.838-3513C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484637 | ||||||
| chr10:13484643
|
A | T | 2 | a0001c0004t0001g0222a0001c0004t0001g0223 | 2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.838-3519T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484643 | ||||||
| chr10:13484705
|
A | G | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.838-3581T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484705 | ||||||
| chr10:13484878
|
T | C | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.838-3754A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13484878 | ||||||
| chr10:13485044
|
C | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(116): Show | 132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.838-3920G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485044 | ||||||
| chr10:13485087
|
G | A | 1 | a0001c0003t0008g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.838-3963C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485087 | ||||||
| chr10:13485179
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.838-4055G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485179 | ||||||
| chr10:13485254
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.838-4130A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485254 | ||||||
| chr10:13485266
|
A | G | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.838-4142T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485266 | ||||||
| chr10:13485544
|
C | A | 7 | a0001c0004t0001g0015a0001c0004t0001g0016a0001c0004t0001g0081others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.838-4420G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485544 | ||||||
| chr10:13485585
|
T | C | 1 | a0001c0002t0001g0155 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.838-4461A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485585 | ||||||
| chr10:13485651
|
G | T | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.838-4527C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485651 | ||||||
| chr10:13485689
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.838-4565A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485689 | ||||||
| chr10:13485860
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.838-4736A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13485860 | ||||||
| chr10:13486028
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0002g0246 | 4 | HG01109.hp1 HG02280.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-4904G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486028 | ||||||
| chr10:13486222
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(129): Show | 147 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.838-5098C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486222 | ||||||
| chr10:13486227
|
G | T | 1 | a0001c0002t0001g0141 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.838-5103C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486227 | ||||||
| chr10:13486236
|
C | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0049others(25): Show | 31 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.838-5112G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486236 | ||||||
| chr10:13486292
|
G | A | 1 | a0001c0003t0001g0009 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.838-5168C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486292 | ||||||
| chr10:13486308
|
C | T | 22 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(19): Show | 22 | HG02572.hp2 HG02602.hp2 HG02735.hp2 others(19): Show |
intron_variant | MODIFIER | c.838-5184G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486308 | ||||||
| chr10:13486344
|
C | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(215): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.838-5220G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486344 | ||||||
| chr10:13486474
|
G | A | 4 | a0001c0002t0001g0142a0001c0002t0001g0144a0001c0002t0001g0156others(1): Show | 4 | HG00280.hp2 HG00741.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-5350C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486474 | ||||||
| chr10:13486756
|
G | A | 4 | a0001c0001t0003g0027a0001c0001t0003g0035a0001c0001t0003g0036others(1): Show | 4 | NA18944.hp1 NA18962.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-5632C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486756 | ||||||
| chr10:13486983
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.837+5628G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13486983 | ||||||
| chr10:13487240
|
T | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(147): Show | 167 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.837+5371A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487240 | ||||||
| chr10:13487362
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(134): Show | 152 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.837+5249C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487362 | ||||||
| chr10:13487381
|
TTC | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.837+5228_837+5229d others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487381 | ||||||
| chr10:13487386
|
T | C | 2 | a0001c0001t0006g0047a0001c0002t0001g0174 | 2 | HG01981.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.837+5225A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487386 | ||||||
| chr10:13487386
|
TTC | T | 51 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0118others(48): Show | 54 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.837+5223_837+5224d others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487386 | ||||||
| chr10:13487387
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.837+5224A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487387 | ||||||
| chr10:13487387
|
TC | T | 27 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0095others(24): Show | 27 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.837+5223delG | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487387 | ||||||
| chr10:13487388
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(137): Show | 155 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.837+5223G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487388 | ||||||
| chr10:13487543
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.837+5068G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487543 | ||||||
| chr10:13487656
|
G | A | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.837+4955C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487656 | ||||||
| chr10:13487678
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(137): Show | 155 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.837+4933T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487678 | ||||||
| chr10:13487738
|
G | GCCAAGCA others(3): Show |
1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4872_837+4873i others(12): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487738 | ||||||
| chr10:13487740
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4871A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487740 | ||||||
| chr10:13487744
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4867G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487744 | ||||||
| chr10:13487747
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4864A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487747 | ||||||
| chr10:13487756
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4855G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487756 | ||||||
| chr10:13487757
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4854G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487757 | ||||||
| chr10:13487759
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4852C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487759 | ||||||
| chr10:13487761
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4850C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487761 | ||||||
| chr10:13487762
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4849C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487762 | ||||||
| chr10:13487765
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4846G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487765 | ||||||
| chr10:13487768
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4843A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487768 | ||||||
| chr10:13487769
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4842A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487769 | ||||||
| chr10:13487771
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4840T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487771 | ||||||
| chr10:13487772
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4839A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487772 | ||||||
| chr10:13487779
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4832C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487779 | ||||||
| chr10:13487785
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4826C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487785 | ||||||
| chr10:13487789
|
T | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(136): Show | 154 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.837+4822A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487789 | ||||||
| chr10:13487794
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4817T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487794 | ||||||
| chr10:13487798
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4813T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487798 | ||||||
| chr10:13487799
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4812T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487799 | ||||||
| chr10:13487803
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4808C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487803 | ||||||
| chr10:13487804
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4807T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487804 | ||||||
| chr10:13487807
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4804A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487807 | ||||||
| chr10:13487809
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4802T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487809 | ||||||
| chr10:13487861
|
G | C | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+4750C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487861 | ||||||
| chr10:13487865
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4746C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487865 | ||||||
| chr10:13487867
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4744A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487867 | ||||||
| chr10:13487868
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4743C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487868 | ||||||
| chr10:13487874
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4737G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487874 | ||||||
| chr10:13487875
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4736A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487875 | ||||||
| chr10:13487880
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4731C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487880 | ||||||
| chr10:13487888
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4723T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487888 | ||||||
| chr10:13487893
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4718A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487893 | ||||||
| chr10:13487901
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4710A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487901 | ||||||
| chr10:13487902
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.837+4709C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13487902 | ||||||
| chr10:13488067
|
T | G | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+4544A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488067 | ||||||
| chr10:13488086
|
C | CA | 12 | a0001c0001t0001g0054a0001c0001t0001g0183a0001c0001t0001g0233others(9): Show | 12 | HG00621.hp1 HG00642.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.837+4524dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488086 | ||||||
| chr10:13488086
|
CAA | C | 19 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(16): Show | 21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.837+4523_837+4524d others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488086 | ||||||
| chr10:13488086
|
CAAA | C | 63 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0087others(60): Show | 64 | HG00140.hp2 HG00408.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.837+4522_837+4524d others(5): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488086 | ||||||
| chr10:13488217
|
T | A | 20 | a0001c0001t0001g0207a0001c0001t0002g0240a0001c0001t0002g0241others(17): Show | 20 | HG00639.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.837+4394A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488217 | ||||||
| chr10:13488320
|
TAAC | T | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.837+4288_837+4290d others(5): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488320 | ||||||
| chr10:13488346
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.837+4265T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488346 | ||||||
| chr10:13488397
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.837+4214T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488397 | ||||||
| chr10:13488461
|
A | G | 1 | a0001c0003t0007g0270 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.837+4150T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488461 | ||||||
| chr10:13488512
|
G | A | 10 | a0001c0001t0001g0058a0001c0001t0006g0044a0001c0001t0006g0047others(7): Show | 12 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+4099C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488512 | ||||||
| chr10:13488546
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0004g0100 | 3 | HG02896.hp2 HG02897.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.837+4065C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488546 | ||||||
| chr10:13488573
|
C | T | 10 | a0001c0003t0001g0005a0001c0003t0001g0121a0001c0003t0001g0123others(7): Show | 12 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+4038G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488573 | ||||||
| chr10:13488636
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0002g0261 | 2 | HG01175.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.837+3975G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488636 | ||||||
| chr10:13488671
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.837+3940A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488671 | ||||||
| chr10:13488679
|
G | A | 1 | a0001c0002t0003g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.837+3932C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488679 | ||||||
| chr10:13488682
|
T | C | 2 | a0001c0002t0001g0103a0001c0002t0001g0186 | 2 | HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.837+3929A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488682 | ||||||
| chr10:13488690
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.837+3921A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488690 | ||||||
| chr10:13488694
|
G | A | 5 | a0001c0001t0001g0204a0001c0001t0001g0219a0001c0003t0001g0126others(2): Show | 5 | HG00621.hp2 HG00673.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+3917C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488694 | ||||||
| chr10:13488701
|
A | C | 13 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0097others(10): Show | 13 | HG02109.hp2 HG02622.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.837+3910T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488701 | ||||||
| chr10:13488702
|
C | T | 13 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0097others(10): Show | 13 | HG02109.hp2 HG02622.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.837+3909G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488702 | ||||||
| chr10:13488703
|
T | G | 13 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0097others(10): Show | 13 | HG02109.hp2 HG02622.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.837+3908A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488703 | ||||||
| chr10:13488709
|
A | G | 13 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0097others(10): Show | 13 | HG02109.hp2 HG02622.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.837+3902T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488709 | ||||||
| chr10:13488711
|
T | A | 13 | a0001c0001t0001g0079a0001c0001t0001g0096a0001c0001t0001g0097others(10): Show | 13 | HG02109.hp2 HG02622.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.837+3900A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488711 | ||||||
| chr10:13488777
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG01361.hp1 HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.837+3834C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488777 | ||||||
| chr10:13488778
|
C | T | 7 | a0001c0003t0001g0005a0001c0003t0001g0042a0001c0003t0001g0121others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.837+3833G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488778 | ||||||
| chr10:13488782
|
C | T | 69 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0075others(66): Show | 72 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.837+3829G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488782 | ||||||
| chr10:13488802
|
G | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0117a0001c0001t0001g0195others(1): Show | 5 | HG02486.hp1 HG02559.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+3809C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488802 | ||||||
| chr10:13488986
|
T | C | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.837+3625A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13488986 | ||||||
| chr10:13489125
|
A | G | 6 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0002g0250others(3): Show | 6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+3486T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489125 | ||||||
| chr10:13489133
|
A | G | 2 | a0001c0002t0001g0166a0001c0002t0001g0170 | 2 | HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.837+3478T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489133 | ||||||
| chr10:13489192
|
G | A | 1 | a0001c0007t0002g0242 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.837+3419C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489192 | ||||||
| chr10:13489210
|
G | A | 3 | a0001c0002t0001g0103a0001c0003t0001g0102a0001c0008t0001g0104 | 3 | HG02015.hp1 HG03942.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.837+3401C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489210 | ||||||
| chr10:13489211
|
G | A | 2 | a0001c0003t0007g0271a0001c0003t0007g0272 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.837+3400C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489211 | ||||||
| chr10:13489381
|
A | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 85 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.837+3230T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489381 | ||||||
| chr10:13489458
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.837+3153C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489458 | ||||||
| chr10:13489517
|
A | G | 1 | a0001c0002t0001g0165 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.837+3094T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489517 | ||||||
| chr10:13489542
|
G | A | 1 | a0001c0002t0001g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.837+3069C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489542 | ||||||
| chr10:13489552
|
T | C | 1 | a0001c0003t0001g0125 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.837+3059A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489552 | ||||||
| chr10:13489692
|
T | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 78 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.837+2919A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489692 | ||||||
| chr10:13489845
|
C | A | 2 | a0001c0003t0007g0271a0001c0003t0007g0272 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.837+2766G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489845 | ||||||
| chr10:13489867
|
G | C | 1 | a0001c0001t0002g0269 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.837+2744C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13489867 | ||||||
| chr10:13490008
|
G | T | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+2603C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490008 | ||||||
| chr10:13490017
|
G | T | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.837+2594C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490017 | ||||||
| chr10:13490077
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.837+2534A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490077 | ||||||
| chr10:13490270
|
C | T | 14 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(11): Show | 14 | HG02602.hp2 HG02735.hp2 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.837+2341G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490270 | ||||||
| chr10:13490300
|
C | T | 2 | a0001c0002t0001g0173a0001c0002t0001g0189 | 2 | HG02135.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.837+2311G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490300 | ||||||
| chr10:13490447
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.837+2164C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490447 | ||||||
| chr10:13490518
|
G | T | 1 | a0001c0002t0001g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.837+2093C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490518 | ||||||
| chr10:13490616
|
G | A | 1 | a0001c0001t0003g0032 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.837+1995C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490616 | ||||||
| chr10:13490648
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(59): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.837+1963G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490648 | ||||||
| chr10:13490798
|
G | T | 1 | a0001c0001t0006g0048 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.837+1813C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13490798 | ||||||
| chr10:13491024
|
G | A | 6 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0002g0250others(3): Show | 6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+1587C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491024 | ||||||
| chr10:13491053
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(69): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.837+1558G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491053 | ||||||
| chr10:13491138
|
A | G | 8 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(5): Show | 8 | HG01891.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.837+1473T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491138 | ||||||
| chr10:13491292
|
G | A | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+1319C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491292 | ||||||
| chr10:13491300
|
G | A | 1 | a0001c0003t0001g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.837+1311C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491300 | ||||||
| chr10:13491311
|
T | TA | 25 | a0001c0001t0001g0038a0001c0001t0001g0072a0001c0001t0001g0093others(22): Show | 25 | HG00544.hp2 HG01175.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.837+1299dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491311 | ||||||
| chr10:13491332
|
A | G | 1 | a0001c0002t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.837+1279T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491332 | ||||||
| chr10:13491333
|
T | A | 1 | a0001c0001t0004g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.837+1278A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491333 | ||||||
| chr10:13491437
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0002g0246 | 3 | HG01109.hp1 HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.837+1174T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491437 | ||||||
| chr10:13491489
|
T | C | 4 | a0001c0002t0001g0143a0001c0002t0001g0158a0001c0002t0001g0185others(1): Show | 4 | HG01952.hp2 NA18972.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.837+1122A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491489 | ||||||
| chr10:13491720
|
C | T | 1 | a0001c0004t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.837+891G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491720 | ||||||
| chr10:13491744
|
T | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 76 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.837+867A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491744 | ||||||
| chr10:13491751
|
C | A | 1 | a0001c0001t0006g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.837+860G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491751 | ||||||
| chr10:13491944
|
T | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(71): Show | 80 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.837+667A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13491944 | ||||||
| chr10:13492031
|
C | T | 6 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0002g0250others(3): Show | 6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+580G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13492031 | ||||||
| chr10:13492234
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.837+377G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13492234 | ||||||
| chr10:13492377
|
G | T | 1 | a0001c0001t0002g0257 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.837+234C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13492377 | ||||||
| chr10:13492526
|
T | C | 2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | HG01361.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.837+85A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13492526 | ||||||
| chr10:13492554
|
T | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 78 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.837+57A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 5/8 | chr10 | 13492554 | ||||||
| chr10:13492891
|
C | A | 2 | a0001c0002t0001g0012a0001c0002t0001g0190 | 3 | NA18747.hp2 NA18975.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.572-15G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13492891 | ||||||
| chr10:13492934
|
A | T | 1 | a0001c0002t0001g0145 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.572-58T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13492934 | ||||||
| chr10:13493223
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 8 | HG01255.hp1 HG01934.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.572-347C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13493223 | ||||||
| chr10:13493317
|
A | T | 72 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 78 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.572-441T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13493317 | ||||||
| chr10:13493351
|
A | ATCATTT | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.572-481_572-476dup others(6): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13493351 | ||||||
| chr10:13493359
|
C | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.572-483G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13493359 | ||||||
| chr10:13493398
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.572-522G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13493398 | ||||||
| chr10:13493773
|
G | C | 3 | a0001c0002t0001g0159a0001c0002t0001g0160a0001c0002t0001g0161 | 3 | HG00558.hp2 HG02129.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.572-897C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13493773 | ||||||
| chr10:13493834
|
A | G | 1 | a0001c0003t0001g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.572-958T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13493834 | ||||||
| chr10:13494073
|
C | A | 66 | a0001c0002t0001g0002a0001c0002t0001g0010a0001c0002t0001g0011others(63): Show | 72 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.572-1197G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13494073 | ||||||
| chr10:13494086
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.572-1210T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13494086 | ||||||
| chr10:13494111
|
T | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 77 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.572-1235A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13494111 | ||||||
| chr10:13494157
|
C | T | 2 | a0001c0003t0007g0271a0001c0003t0007g0272 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.572-1281G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13494157 | ||||||
| chr10:13494365
|
C | T | 1 | a0001c0003t0001g0005 | 3 | HG02647.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.572-1489G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13494365 | ||||||
| chr10:13494384
|
T | C | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.572-1508A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13494384 | ||||||
| chr10:13494512
|
A | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.572-1636T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13494512 | ||||||
| chr10:13494644
|
C | T | 1 | a0001c0003t0005g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.572-1768G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13494644 | ||||||
| chr10:13495106
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.571+1660A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13495106 | ||||||
| chr10:13495204
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.571+1562C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13495204 | ||||||
| chr10:13495263
|
C | T | 1 | a0001c0003t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.571+1503G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13495263 | ||||||
| chr10:13495287
|
C | T | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.571+1479G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13495287 | ||||||
| chr10:13495610
|
C | T | 1 | a0001c0004t0001g0205 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.571+1156G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13495610 | ||||||
| chr10:13495805
|
T | C | 1 | a0001c0002t0001g0170 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.571+961A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13495805 | ||||||
| chr10:13495935
|
T | C | 1 | a0001c0003t0001g0102 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.571+831A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13495935 | ||||||
| chr10:13496200
|
G | A | 1 | a0001c0004t0003g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.571+566C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13496200 | ||||||
| chr10:13496332
|
A | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG00609.hp2 NA18949.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.571+434T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13496332 | ||||||
| chr10:13496334
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.571+432C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 4/8 | chr10 | 13496334 | ||||||
| chr10:13496928
|
C | CA | 27 | a0001c0002t0001g0103a0001c0003t0001g0005a0001c0003t0001g0009others(24): Show | 30 | HG01081.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.449-41dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13496928 | ||||||
| chr10:13496928
|
C | CAA | 75 | a0001c0001t0001g0202a0001c0001t0001g0226a0001c0001t0002g0263others(72): Show | 81 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.449-42_449-41dupTT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13496928 | ||||||
| chr10:13496928
|
C | CAAA | 61 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 67 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.449-43_449-41dupTT others(1): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13496928 | ||||||
| chr10:13496928
|
C | CAAAA | 9 | a0001c0001t0001g0204a0001c0001t0001g0216a0001c0001t0001g0217others(6): Show | 9 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.449-44_449-41dupTT others(2): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13496928 | ||||||
| chr10:13496928
|
CA | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(88): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.449-41delT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13496928 | ||||||
| chr10:13497134
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0066 | 3 | HG00642.hp1 HG01515.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.449-246G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13497134 | ||||||
| chr10:13497433
|
T | C | 1 | a0001c0003t0001g0164 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.449-545A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13497433 | ||||||
| chr10:13497446
|
A | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 7 | HG00408.hp2 NA18747.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-558T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13497446 | ||||||
| chr10:13497623
|
G | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 75 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.449-735C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13497623 | ||||||
| chr10:13497704
|
A | G | 13 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(10): Show | 13 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.449-816T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13497704 | ||||||
| chr10:13497746
|
C | T | 13 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(10): Show | 13 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.449-858G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13497746 | ||||||
| chr10:13497787
|
A | G | 1 | a0001c0003t0001g0121 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.449-899T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13497787 | ||||||
| chr10:13497835
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 76 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.449-947A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13497835 | ||||||
| chr10:13497957
|
A | G | 1 | a0001c0003t0001g0128 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.449-1069T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13497957 | ||||||
| chr10:13498037
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.449-1149T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498037 | ||||||
| chr10:13498055
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 76 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.449-1167A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498055 | ||||||
| chr10:13498071
|
C | CT | 7 | a0001c0002t0001g0144a0001c0002t0001g0181a0001c0002t0001g0187others(4): Show | 7 | HG00741.hp1 HG02155.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1184dupA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498071 | ||||||
| chr10:13498071
|
CT | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(84): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.449-1184delA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498071 | ||||||
| chr10:13498071
|
CTTTTTT | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 76 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.449-1189_449-1184d others(8): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498071 | ||||||
| chr10:13498217
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.449-1329T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498217 | ||||||
| chr10:13498358
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 75 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.448+1420G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498358 | ||||||
| chr10:13498500
|
C | A | 6 | a0001c0003t0001g0112a0001c0003t0001g0122a0001c0003t0001g0123others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+1278G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498500 | ||||||
| chr10:13498500
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.448+1278G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498500 | ||||||
| chr10:13498501
|
A | G | 6 | a0001c0003t0001g0112a0001c0003t0001g0122a0001c0003t0001g0123others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+1277T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498501 | ||||||
| chr10:13498537
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(86): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.448+1241A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498537 | ||||||
| chr10:13498724
|
G | T | 68 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 74 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.448+1054C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498724 | ||||||
| chr10:13498869
|
A | C | 67 | a0001c0001t0001g0171a0001c0002t0001g0002a0001c0002t0001g0010others(64): Show | 73 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.448+909T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498869 | ||||||
| chr10:13498873
|
A | G | 2 | a0001c0003t0007g0271a0001c0003t0007g0272 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.448+905T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13498873 | ||||||
| chr10:13499008
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(86): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.448+770A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13499008 | ||||||
| chr10:13499272
|
T | C | 2 | a0001c0003t0004g0113a0001c0003t0004g0114 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.448+506A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13499272 | ||||||
| chr10:13499274
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 76 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.448+504A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13499274 | ||||||
| chr10:13499516
|
G | A | 1 | a0001c0007t0002g0242 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.448+262C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13499516 | ||||||
| chr10:13499575
|
C | T | 1 | a0001c0001t0004g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.448+203G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13499575 | ||||||
| chr10:13499724
|
T | TAAAAC | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.448+53_448+54insGT others(3): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 3/8 | chr10 | 13499724 | ||||||
| chr10:13500130
|
A | G | 13 | a0001c0003t0001g0005a0001c0003t0001g0112a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.146-50T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13500130 | ||||||
| chr10:13500425
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.146-345A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13500425 | ||||||
| chr10:13500712
|
C | T | 3 | a0002c0005t0002g0243a0002c0005t0002g0244a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.146-632G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13500712 | ||||||
| chr10:13500754
|
C | G | 5 | a0001c0003t0001g0109a0001c0003t0004g0110a0001c0003t0004g0111others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-674G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13500754 | ||||||
| chr10:13500757
|
G | T | 9 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0004t0001g0015others(6): Show | 11 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.146-677C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13500757 | ||||||
| chr10:13500761
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.146-681A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13500761 | ||||||
| chr10:13501374
|
CA | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(184): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.146-1295delT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501374 | ||||||
| chr10:13501374
|
CAA | C | 80 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 88 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.146-1296_146-1295d others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501374 | ||||||
| chr10:13501383
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.146-1303T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501383 | ||||||
| chr10:13501391
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.146-1311T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501391 | ||||||
| chr10:13501493
|
C | A | 11 | a0001c0001t0001g0171a0001c0002t0001g0002a0001c0002t0001g0134others(8): Show | 14 | HG00735.hp1 HG00738.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.146-1413G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501493 | ||||||
| chr10:13501512
|
G | T | 1 | a0004c0010t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.146-1432C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501512 | ||||||
| chr10:13501825
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.146-1745C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501825 | ||||||
| chr10:13501842
|
T | C | 1 | a0001c0004t0001g0223 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.146-1762A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501842 | ||||||
| chr10:13501845
|
CA | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.146-1766delT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501845 | ||||||
| chr10:13501855
|
A | C | 1 | a0001c0004t0001g0203 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.146-1775T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501855 | ||||||
| chr10:13501867
|
C | T | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-1787G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13501867 | ||||||
| chr10:13502057
|
G | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.146-1977C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502057 | ||||||
| chr10:13502063
|
G | GTA | 69 | a0001c0001t0001g0171a0001c0002t0001g0002a0001c0002t0001g0010others(66): Show | 75 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.146-1985_146-1984d others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502063 | ||||||
| chr10:13502285
|
A | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.146-2205T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502285 | ||||||
| chr10:13502526
|
G | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.146-2446C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502526 | ||||||
| chr10:13502585
|
A | G | 68 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 74 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.146-2505T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502585 | ||||||
| chr10:13502619
|
C | T | 1 | a0001c0003t0001g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.146-2539G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502619 | ||||||
| chr10:13502763
|
G | C | 1 | a0001c0006t0004g0106 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.146-2683C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502763 | ||||||
| chr10:13502786
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 76 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.146-2706A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502786 | ||||||
| chr10:13502828
|
G | A | 1 | a0001c0001t0005g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.146-2748C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502828 | ||||||
| chr10:13502854
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(69): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.146-2774A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502854 | ||||||
| chr10:13502864
|
G | A | 68 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 74 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.146-2784C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502864 | ||||||
| chr10:13502913
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.146-2833G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13502913 | ||||||
| chr10:13503051
|
T | C | 1 | a0001c0004t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.146-2971A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503051 | ||||||
| chr10:13503130
|
A | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 74 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.146-3050T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503130 | ||||||
| chr10:13503224
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.146-3144G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503224 | ||||||
| chr10:13503225
|
G | A | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.146-3145C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503225 | ||||||
| chr10:13503268
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.146-3188G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503268 | ||||||
| chr10:13503325
|
T | C | 1 | a0001c0003t0005g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.146-3245A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503325 | ||||||
| chr10:13503481
|
C | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.146-3401G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503481 | ||||||
| chr10:13503489
|
G | A | 1 | a0001c0002t0001g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.146-3409C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503489 | ||||||
| chr10:13503495
|
C | T | 1 | a0001c0003t0002g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.146-3415G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503495 | ||||||
| chr10:13503496
|
C | T | 1 | a0001c0002t0001g0143 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.146-3416G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503496 | ||||||
| chr10:13503577
|
G | A | 3 | a0001c0002t0001g0103a0001c0003t0001g0102a0001c0008t0001g0104 | 3 | HG02015.hp1 HG03942.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.146-3497C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503577 | ||||||
| chr10:13503584
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(138): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.146-3504C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503584 | ||||||
| chr10:13503712
|
A | AAAAC | 4 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0066others(1): Show | 4 | HG00642.hp1 HG01515.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3636_146-3633d others(6): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503712 | ||||||
| chr10:13503712
|
A | AAAACAAA others(1): Show |
65 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(62): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.146-3640_146-3633d others(10): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503712 | ||||||
| chr10:13503712
|
A | AAAACAAA others(5): Show |
2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.146-3644_146-3633d others(14): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503712 | ||||||
| chr10:13503916
|
C | A | 1 | a0001c0004t0001g0200 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.146-3836G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13503916 | ||||||
| chr10:13504074
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.146-3994C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504074 | ||||||
| chr10:13504095
|
G | A | 2 | a0001c0002t0001g0173a0001c0002t0001g0189 | 2 | HG02135.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.146-4015C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504095 | ||||||
| chr10:13504119
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0056others(3): Show | 9 | HG01081.hp1 HG01255.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.146-4039T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504119 | ||||||
| chr10:13504192
|
G | T | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.146-4112C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504192 | ||||||
| chr10:13504343
|
GC | G | 7 | a0001c0003t0001g0005a0001c0003t0001g0121a0001c0003t0001g0126others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.146-4264delG | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504343 | ||||||
| chr10:13504394
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.146-4314C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504394 | ||||||
| chr10:13504444
|
T | C | 1 | a0001c0003t0001g0179 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.146-4364A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504444 | ||||||
| chr10:13504514
|
T | C | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.146-4434A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504514 | ||||||
| chr10:13504707
|
G | A | 14 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(11): Show | 14 | HG02602.hp2 HG02735.hp2 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.146-4627C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504707 | ||||||
| chr10:13504892
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.146-4812A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504892 | ||||||
| chr10:13504936
|
G | GATA | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-4859_146-4857d others(5): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504936 | ||||||
| chr10:13504988
|
G | T | 1 | a0001c0001t0002g0246 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.146-4908C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13504988 | ||||||
| chr10:13505197
|
C | G | 1 | a0001c0008t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.146-5117G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505197 | ||||||
| chr10:13505225
|
T | A | 2 | a0001c0003t0007g0271a0001c0003t0007g0272 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146-5145A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505225 | ||||||
| chr10:13505227
|
A | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.146-5147T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505227 | ||||||
| chr10:13505244
|
G | C | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.146-5164C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505244 | ||||||
| chr10:13505245
|
C | T | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.146-5165G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505245 | ||||||
| chr10:13505264
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.146-5184G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505264 | ||||||
| chr10:13505405
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 75 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.146-5325G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505405 | ||||||
| chr10:13505507
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(67): Show | 76 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.146-5427G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505507 | ||||||
| chr10:13505709
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(170): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.146-5629T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505709 | ||||||
| chr10:13505746
|
C | T | 2 | a0001c0001t0002g0254a0001c0001t0002g0256 | 2 | HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.146-5666G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505746 | ||||||
| chr10:13505964
|
C | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(198): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.146-5884G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13505964 | ||||||
| chr10:13506137
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0066 | 3 | HG00642.hp1 HG01515.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.146-6057G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506137 | ||||||
| chr10:13506200
|
CCT | C | 18 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(15): Show | 18 | HG02602.hp2 HG02622.hp1 HG02735.hp2 others(15): Show |
intron_variant | MODIFIER | c.146-6122_146-6121d others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506200 | ||||||
| chr10:13506225
|
T | C | 14 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(11): Show | 14 | HG02602.hp2 HG02735.hp2 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.146-6145A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506225 | ||||||
| chr10:13506287
|
T | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0217a0001c0001t0001g0219others(1): Show | 4 | HG00621.hp2 HG00673.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-6207A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506287 | ||||||
| chr10:13506332
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(196): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.146-6252G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506332 | ||||||
| chr10:13506340
|
C | T | 1 | a0001c0003t0001g0009 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.146-6260G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506340 | ||||||
| chr10:13506360
|
G | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 75 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.146-6280C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506360 | ||||||
| chr10:13506477
|
A | C | 3 | a0002c0005t0002g0243a0002c0005t0002g0244a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.146-6397T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506477 | ||||||
| chr10:13506723
|
G | A | 12 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(9): Show | 12 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.146-6643C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506723 | ||||||
| chr10:13506764
|
G | GGA | 74 | a0001c0001t0001g0171a0001c0002t0001g0002a0001c0002t0001g0010others(71): Show | 80 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.146-6686_146-6685d others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506764 | ||||||
| chr10:13506827
|
T | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(196): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.146-6747A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506827 | ||||||
| chr10:13506842
|
G | A | 1 | a0001c0002t0001g0182 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.146-6762C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13506842 | ||||||
| chr10:13507093
|
G | T | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.146-7013C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507093 | ||||||
| chr10:13507099
|
G | C | 1 | a0001c0003t0001g0179 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.146-7019C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507099 | ||||||
| chr10:13507127
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.146-7047A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507127 | ||||||
| chr10:13507226
|
A | T | 2 | a0001c0003t0001g0126a0001c0003t0001g0127 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.146-7146T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507226 | ||||||
| chr10:13507280
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(197): Show | 218 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.146-7200G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507280 | ||||||
| chr10:13507304
|
G | A | 1 | a0001c0003t0001g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.146-7224C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507304 | ||||||
| chr10:13507324
|
G | C | 1 | a0001c0004t0001g0224 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.146-7244C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507324 | ||||||
| chr10:13507379
|
G | C | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.146-7299C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507379 | ||||||
| chr10:13507397
|
G | A | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.146-7317C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507397 | ||||||
| chr10:13507444
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0226 | 2 | HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.146-7364C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507444 | ||||||
| chr10:13507462
|
G | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.146-7382C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507462 | ||||||
| chr10:13507751
|
A | T | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-7671T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507751 | ||||||
| chr10:13507769
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0219 | 2 | HG00621.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.146-7689C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507769 | ||||||
| chr10:13507825
|
C | T | 68 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 74 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.146-7745G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507825 | ||||||
| chr10:13507843
|
G | C | 2 | a0001c0003t0001g0177a0001c0003t0001g0178 | 2 | HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.146-7763C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507843 | ||||||
| chr10:13507927
|
C | G | 68 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 74 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.146-7847G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13507927 | ||||||
| chr10:13508259
|
G | A | 2 | a0001c0002t0001g0174a0001c0007t0002g0242 | 2 | HG01981.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.146-8179C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13508259 | ||||||
| chr10:13508400
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.146-8320G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13508400 | ||||||
| chr10:13508467
|
T | C | 2 | a0001c0003t0007g0271a0001c0003t0007g0272 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146-8387A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13508467 | ||||||
| chr10:13508822
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.146-8742T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13508822 | ||||||
| chr10:13508872
|
C | G | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-8792G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13508872 | ||||||
| chr10:13508915
|
G | A | 1 | a0001c0001t0004g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.146-8835C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13508915 | ||||||
| chr10:13509131
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.146-9051A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13509131 | ||||||
| chr10:13509344
|
G | C | 1 | a0001c0003t0001g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.146-9264C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13509344 | ||||||
| chr10:13509357
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.146-9277G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13509357 | ||||||
| chr10:13509783
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.146-9703C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13509783 | ||||||
| chr10:13509850
|
G | A | 1 | a0001c0002t0001g0239 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.146-9770C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13509850 | ||||||
| chr10:13509855
|
C | G | 1 | a0001c0002t0001g0142 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.146-9775G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13509855 | ||||||
| chr10:13509876
|
C | T | 82 | a0001c0001t0001g0171a0001c0002t0001g0002a0001c0002t0001g0010others(79): Show | 89 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.146-9796G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13509876 | ||||||
| chr10:13509944
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.146-9864G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13509944 | ||||||
| chr10:13510071
|
C | G | 14 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(11): Show | 14 | HG02602.hp2 HG02735.hp2 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.146-9991G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13510071 | ||||||
| chr10:13510552
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.146-10472G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13510552 | ||||||
| chr10:13510627
|
A | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 75 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.146-10547T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13510627 | ||||||
| chr10:13510745
|
T | C | 1 | a0001c0003t0002g0249 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.146-10665A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13510745 | ||||||
| chr10:13510900
|
G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0002g0240others(19): Show | 24 | HG00609.hp1 HG01167.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.146-10820C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13510900 | ||||||
| chr10:13510975
|
C | T | 81 | a0001c0001t0001g0171a0001c0002t0001g0002a0001c0002t0001g0010others(78): Show | 88 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.146-10895G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13510975 | ||||||
| chr10:13511256
|
T | C | 1 | a0004c0010t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.146-11176A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13511256 | ||||||
| chr10:13511265
|
A | G | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-11185T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13511265 | ||||||
| chr10:13511266
|
C | T | 5 | a0001c0003t0001g0122a0001c0003t0001g0123a0001c0003t0001g0124others(2): Show | 5 | HG02257.hp1 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-11186G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13511266 | ||||||
| chr10:13511345
|
T | C | 34 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(31): Show | 36 | HG00639.hp2 HG01081.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.146-11265A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13511345 | ||||||
| chr10:13511391
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0040others(49): Show | 57 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.146-11311C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13511391 | ||||||
| chr10:13511521
|
G | A | 2 | a0001c0003t0001g0175a0001c0003t0001g0176 | 2 | NA18942.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.146-11441C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13511521 | ||||||
| chr10:13511724
|
T | C | 1 | a0001c0003t0001g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.146-11644A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13511724 | ||||||
| chr10:13511848
|
T | C | 1 | a0001c0002t0001g0182 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.146-11768A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13511848 | ||||||
| chr10:13512214
|
C | T | 5 | a0001c0003t0001g0122a0001c0003t0001g0123a0001c0003t0001g0124others(2): Show | 5 | HG02257.hp1 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-12134G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13512214 | ||||||
| chr10:13512431
|
G | C | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-12351C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13512431 | ||||||
| chr10:13512502
|
A | G | 2 | a0001c0003t0007g0271a0001c0003t0007g0272 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146-12422T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13512502 | ||||||
| chr10:13512660
|
A | G | 3 | a0001c0001t0001g0208a0001c0004t0001g0200a0001c0004t0001g0209 | 3 | HG00673.hp1 HG03492.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.146-12580T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13512660 | ||||||
| chr10:13512693
|
G | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.146-12613C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13512693 | ||||||
| chr10:13512909
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.146-12829G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13512909 | ||||||
| chr10:13513118
|
A | C | 5 | a0001c0003t0001g0122a0001c0003t0001g0123a0001c0003t0001g0124others(2): Show | 5 | HG02257.hp1 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+13020T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513118 | ||||||
| chr10:13513141
|
G | A | 1 | a0001c0003t0001g0128 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.145+12997C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513141 | ||||||
| chr10:13513216
|
G | T | 2 | a0001c0002t0001g0012a0001c0002t0001g0190 | 3 | NA18747.hp2 NA18975.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.145+12922C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513216 | ||||||
| chr10:13513222
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0052others(2): Show | 6 | HG00735.hp2 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+12916G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513222 | ||||||
| chr10:13513278
|
G | A | 2 | a0001c0004t0002g0255a0001c0004t0002g0266 | 2 | HG00609.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.145+12860C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513278 | ||||||
| chr10:13513305
|
G | A | 1 | a0001c0008t0001g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.145+12833C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513305 | ||||||
| chr10:13513545
|
C | T | 5 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0007g0270others(2): Show | 5 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+12593G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513545 | ||||||
| chr10:13513549
|
C | T | 34 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(31): Show | 36 | HG00639.hp2 HG01081.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.145+12589G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513549 | ||||||
| chr10:13513558
|
C | T | 1 | a0001c0004t0001g0015 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.145+12580G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513558 | ||||||
| chr10:13513820
|
C | T | 2 | a0001c0004t0001g0222a0001c0004t0001g0223 | 2 | HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.145+12318G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513820 | ||||||
| chr10:13513897
|
C | T | 13 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(10): Show | 13 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.145+12241G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513897 | ||||||
| chr10:13513905
|
C | T | 1 | a0001c0006t0004g0105 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.145+12233G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513905 | ||||||
| chr10:13513913
|
A | G | 6 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0002g0250others(3): Show | 6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+12225T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513913 | ||||||
| chr10:13513986
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.145+12152G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13513986 | ||||||
| chr10:13514090
|
T | TTTCAAG | 274 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.145+12047_145+1204 others(10): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514090 | ||||||
| chr10:13514277
|
T | A | 1 | a0001c0001t0001g0067 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.145+11861A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514277 | ||||||
| chr10:13514280
|
C | T | 1 | a0001c0003t0001g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.145+11858G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514280 | ||||||
| chr10:13514397
|
G | A | 9 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0002g0250others(6): Show | 9 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.145+11741C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514397 | ||||||
| chr10:13514429
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 73 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.145+11709G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514429 | ||||||
| chr10:13514437
|
T | A | 14 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(11): Show | 14 | HG02602.hp2 HG02735.hp2 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.145+11701A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514437 | ||||||
| chr10:13514487
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.145+11651A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514487 | ||||||
| chr10:13514534
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.145+11604G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514534 | ||||||
| chr10:13514587
|
AG | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.145+11550delC | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514587 | ||||||
| chr10:13514634
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.145+11504C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514634 | ||||||
| chr10:13514817
|
G | A | 1 | a0005c0012t0014g0273 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.145+11321C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13514817 | ||||||
| chr10:13515085
|
T | C | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.145+11053A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13515085 | ||||||
| chr10:13515103
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(200): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.145+11035A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13515103 | ||||||
| chr10:13515277
|
T | G | 1 | a0001c0002t0001g0134 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.145+10861A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13515277 | ||||||
| chr10:13515512
|
G | T | 1 | a0001c0002t0001g0239 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.145+10626C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13515512 | ||||||
| chr10:13515581
|
G | A | 2 | a0001c0003t0001g0175a0001c0003t0001g0176 | 2 | NA18942.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.145+10557C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13515581 | ||||||
| chr10:13515945
|
G | C | 71 | a0001c0001t0001g0171a0001c0001t0001g0221a0001c0002t0001g0002others(68): Show | 77 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.145+10193C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13515945 | ||||||
| chr10:13515960
|
A | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0073others(23): Show | 29 | HG00544.hp2 HG00609.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.145+10178T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13515960 | ||||||
| chr10:13516070
|
G | T | 1 | a0001c0001t0001g0040 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.145+10068C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516070 | ||||||
| chr10:13516108
|
A | T | 1 | a0001c0001t0003g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.145+10030T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516108 | ||||||
| chr10:13516126
|
A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.145+10012T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516126 | ||||||
| chr10:13516149
|
T | C | 68 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 74 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.145+9989A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516149 | ||||||
| chr10:13516299
|
C | T | 14 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(11): Show | 14 | HG02602.hp2 HG02735.hp2 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.145+9839G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516299 | ||||||
| chr10:13516451
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+9687G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516451 | ||||||
| chr10:13516516
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(199): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.145+9622C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516516 | ||||||
| chr10:13516555
|
G | A | 2 | a0001c0003t0001g0177a0001c0003t0001g0178 | 2 | HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.145+9583C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516555 | ||||||
| chr10:13516560
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.145+9578G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516560 | ||||||
| chr10:13516641
|
G | A | 68 | a0001c0001t0001g0171a0001c0002t0001g0002a0001c0002t0001g0010others(65): Show | 74 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.145+9497C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516641 | ||||||
| chr10:13516706
|
C | T | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+9432G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516706 | ||||||
| chr10:13516815
|
G | T | 1 | a0001c0004t0001g0205 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.145+9323C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516815 | ||||||
| chr10:13516821
|
T | C | 4 | a0001c0003t0001g0005a0001c0003t0001g0120a0001c0003t0001g0121others(1): Show | 6 | HG01891.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.145+9317A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516821 | ||||||
| chr10:13516983
|
A | G | 1 | a0001c0002t0001g0141 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.145+9155T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13516983 | ||||||
| chr10:13517043
|
C | T | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.145+9095G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517043 | ||||||
| chr10:13517065
|
C | CT | 7 | a0001c0001t0001g0204a0001c0002t0001g0137a0001c0002t0001g0139others(4): Show | 7 | HG00544.hp1 HG00621.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.145+9072dupA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517065 | ||||||
| chr10:13517065
|
CT | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.145+9072delA | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517065 | ||||||
| chr10:13517065
|
CTTTTTT | C | 8 | a0001c0003t0002g0247a0001c0003t0002g0249a0001c0003t0002g0250others(5): Show | 8 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.145+9067_145+9072d others(8): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517065 | ||||||
| chr10:13517076
|
T | C | 1 | a0001c0003t0002g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.145+9062A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517076 | ||||||
| chr10:13517126
|
G | A | 2 | a0001c0003t0004g0113a0001c0003t0004g0114 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.145+9012C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517126 | ||||||
| chr10:13517128
|
T | C | 6 | a0001c0001t0005g0022a0001c0003t0005g0017a0001c0003t0005g0018others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+9010A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517128 | ||||||
| chr10:13517157
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(201): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.145+8981A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517157 | ||||||
| chr10:13517269
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0003t0001g0129 | 3 | HG01884.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.145+8869C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517269 | ||||||
| chr10:13517509
|
G | A | 1 | a0001c0002t0001g0134 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.145+8629C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517509 | ||||||
| chr10:13517545
|
C | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.145+8593G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517545 | ||||||
| chr10:13517698
|
C | T | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.145+8440G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517698 | ||||||
| chr10:13517751
|
T | C | 14 | a0001c0001t0001g0045a0001c0001t0005g0022a0001c0001t0006g0044others(11): Show | 14 | HG01891.hp1 HG02258.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.145+8387A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517751 | ||||||
| chr10:13517754
|
A | G | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.145+8384T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517754 | ||||||
| chr10:13517793
|
G | A | 8 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(5): Show | 8 | HG01891.hp1 HG02602.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.145+8345C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517793 | ||||||
| chr10:13517822
|
T | C | 1 | a0001c0002t0001g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.145+8316A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517822 | ||||||
| chr10:13517929
|
G | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(199): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.145+8209C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517929 | ||||||
| chr10:13517981
|
A | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.145+8157T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13517981 | ||||||
| chr10:13518021
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.145+8117A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518021 | ||||||
| chr10:13518107
|
A | G | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+8031T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518107 | ||||||
| chr10:13518170
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.145+7968T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518170 | ||||||
| chr10:13518200
|
T | C | 1 | a0001c0001t0002g0268 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.145+7938A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518200 | ||||||
| chr10:13518286
|
A | AGCAGGCT | 57 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 61 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.145+7845_145+7851d others(9): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518286 | ||||||
| chr10:13518368
|
G | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+7770C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518368 | ||||||
| chr10:13518576
|
C | A | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+7562G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518576 | ||||||
| chr10:13518719
|
T | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(66): Show | 75 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.145+7419A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518719 | ||||||
| chr10:13518763
|
G | A | 6 | a0001c0002t0001g0012a0001c0002t0001g0181a0001c0002t0001g0182others(3): Show | 7 | HG02155.hp1 NA18747.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.145+7375C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518763 | ||||||
| chr10:13518871
|
A | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(58): Show | 70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.145+7267T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518871 | ||||||
| chr10:13518872
|
T | C | 3 | a0001c0002t0001g0103a0001c0003t0001g0102a0001c0008t0001g0104 | 3 | HG02015.hp1 HG03942.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.145+7266A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518872 | ||||||
| chr10:13518937
|
A | C | 1 | a0001c0004t0001g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.145+7201T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518937 | ||||||
| chr10:13518949
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.145+7189C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13518949 | ||||||
| chr10:13519048
|
T | G | 6 | a0001c0001t0005g0022a0001c0003t0005g0017a0001c0003t0005g0018others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+7090A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519048 | ||||||
| chr10:13519049
|
C | T | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+7089G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519049 | ||||||
| chr10:13519255
|
G | A | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+6883C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519255 | ||||||
| chr10:13519336
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.145+6802A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519336 | ||||||
| chr10:13519369
|
G | A | 7 | a0001c0001t0005g0022a0001c0002t0003g0034a0001c0003t0005g0017others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.145+6769C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519369 | ||||||
| chr10:13519393
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 73 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.145+6745C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519393 | ||||||
| chr10:13519401
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.145+6737C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519401 | ||||||
| chr10:13519488
|
G | GA | 100 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(97): Show | 109 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.145+6649dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519488 | ||||||
| chr10:13519611
|
C | T | 2 | a0001c0006t0004g0105a0001c0006t0004g0106 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.145+6527G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519611 | ||||||
| chr10:13519616
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.145+6522C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519616 | ||||||
| chr10:13519779
|
G | A | 1 | a0001c0003t0001g0005 | 3 | HG02647.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.145+6359C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519779 | ||||||
| chr10:13519808
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.145+6330C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519808 | ||||||
| chr10:13519888
|
G | A | 13 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(10): Show | 13 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.145+6250C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519888 | ||||||
| chr10:13519956
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.145+6182C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519956 | ||||||
| chr10:13519976
|
T | G | 3 | a0002c0005t0002g0243a0002c0005t0002g0244a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.145+6162A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13519976 | ||||||
| chr10:13520003
|
G | A | 7 | a0001c0003t0001g0005a0001c0003t0001g0121a0001c0003t0001g0126others(4): Show | 9 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+6135C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520003 | ||||||
| chr10:13520009
|
G | C | 1 | a0001c0003t0001g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.145+6129C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520009 | ||||||
| chr10:13520075
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.145+6063C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520075 | ||||||
| chr10:13520076
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(199): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.145+6062A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520076 | ||||||
| chr10:13520322
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(199): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.145+5816T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520322 | ||||||
| chr10:13520413
|
C | A | 12 | a0001c0003t0001g0005a0001c0003t0001g0121a0001c0003t0001g0122others(9): Show | 14 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.145+5725G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520413 | ||||||
| chr10:13520414
|
G | A | 6 | a0001c0001t0005g0022a0001c0003t0005g0017a0001c0003t0005g0018others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+5724C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520414 | ||||||
| chr10:13520434
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+5704G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520434 | ||||||
| chr10:13520458
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.145+5680C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520458 | ||||||
| chr10:13520471
|
A | C | 18 | a0001c0001t0001g0045a0001c0001t0001g0095a0001c0001t0003g0026others(15): Show | 18 | HG02602.hp1 HG02602.hp2 HG02735.hp2 others(15): Show |
intron_variant | MODIFIER | c.145+5667T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520471 | ||||||
| chr10:13520483
|
G | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.145+5655C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520483 | ||||||
| chr10:13520575
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.145+5563C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520575 | ||||||
| chr10:13520740
|
C | T | 1 | a0001c0004t0002g0255 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.145+5398G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520740 | ||||||
| chr10:13520823
|
T | G | 13 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(10): Show | 13 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.145+5315A>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520823 | ||||||
| chr10:13520833
|
T | C | 2 | a0001c0002t0001g0011a0001c0003t0001g0193 | 3 | HG00408.hp1 HG01943.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.145+5305A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520833 | ||||||
| chr10:13520883
|
C | T | 13 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(10): Show | 13 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.145+5255G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520883 | ||||||
| chr10:13520924
|
C | T | 4 | a0001c0001t0003g0027a0001c0001t0003g0035a0001c0001t0003g0036others(1): Show | 4 | NA18944.hp1 NA18962.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+5214G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520924 | ||||||
| chr10:13520975
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.145+5163A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13520975 | ||||||
| chr10:13521083
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG03130.hp2 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.145+5055G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521083 | ||||||
| chr10:13521091
|
C | T | 15 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(12): Show | 15 | HG02602.hp2 HG02735.hp2 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.145+5047G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521091 | ||||||
| chr10:13521127
|
C | T | 1 | a0001c0003t0001g0121 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.145+5011G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521127 | ||||||
| chr10:13521267
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.145+4871G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521267 | ||||||
| chr10:13521382
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG00609.hp2 NA18949.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.145+4756A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521382 | ||||||
| chr10:13521425
|
G | A | 1 | a0005c0012t0014g0273 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.145+4713C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521425 | ||||||
| chr10:13521439
|
T | C | 15 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(12): Show | 15 | HG02602.hp2 HG02735.hp2 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.145+4699A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521439 | ||||||
| chr10:13521734
|
C | G | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+4404G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521734 | ||||||
| chr10:13521816
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(35): Show | 45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.145+4322A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521816 | ||||||
| chr10:13521964
|
G | C | 1 | a0001c0002t0001g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.145+4174C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13521964 | ||||||
| chr10:13522130
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(133): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.145+4008T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13522130 | ||||||
| chr10:13522132
|
T | TTC | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.145+4005_145+4006i others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13522132 | ||||||
| chr10:13522414
|
C | G | 1 | a0001c0002t0001g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.145+3724G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13522414 | ||||||
| chr10:13522616
|
C | T | 2 | a0001c0003t0001g0005a0004c0010t0001g0119 | 4 | HG01891.hp2 HG02647.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+3522G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13522616 | ||||||
| chr10:13523111
|
A | G | 14 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(11): Show | 14 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.145+3027T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13523111 | ||||||
| chr10:13523115
|
C | A | 1 | a0001c0001t0006g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.145+3023G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13523115 | ||||||
| chr10:13523230
|
A | T | 1 | a0001c0001t0001g0039 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.145+2908T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13523230 | ||||||
| chr10:13523279
|
C | A | 1 | a0001c0002t0001g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.145+2859G>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13523279 | ||||||
| chr10:13523336
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.145+2802A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13523336 | ||||||
| chr10:13523429
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(104): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.145+2709C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13523429 | ||||||
| chr10:13523886
|
C | T | 1 | a0001c0001t0004g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.145+2252G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13523886 | ||||||
| chr10:13524013
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(133): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.145+2125G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524013 | ||||||
| chr10:13524204
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(133): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.145+1934T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524204 | ||||||
| chr10:13524215
|
G | A | 1 | a0001c0004t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.145+1923C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524215 | ||||||
| chr10:13524346
|
A | G | 3 | a0001c0002t0001g0103a0001c0003t0001g0102a0001c0008t0001g0104 | 3 | HG02015.hp1 HG03942.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.145+1792T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524346 | ||||||
| chr10:13524359
|
C | T | 6 | a0001c0001t0005g0022a0001c0003t0005g0017a0001c0003t0005g0018others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+1779G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524359 | ||||||
| chr10:13524362
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(133): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.145+1776T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524362 | ||||||
| chr10:13524368
|
C | T | 7 | a0001c0001t0002g0246a0001c0003t0002g0247a0001c0003t0002g0249others(4): Show | 7 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.145+1770G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524368 | ||||||
| chr10:13524559
|
G | A | 1 | a0001c0001t0002g0269 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.145+1579C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524559 | ||||||
| chr10:13524644
|
CA | C | 25 | a0001c0001t0002g0253a0001c0001t0003g0035a0001c0001t0003g0036others(22): Show | 25 | HG01081.hp2 HG02015.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.145+1493delT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524644 | ||||||
| chr10:13524644
|
CAA | C | 35 | a0001c0001t0001g0071a0001c0001t0001g0095a0001c0001t0002g0246others(32): Show | 37 | HG00639.hp2 HG01884.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.145+1492_145+1493d others(4): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524644 | ||||||
| chr10:13524644
|
CAAA | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.145+1491_145+1493d others(5): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524644 | ||||||
| chr10:13524644
|
CAAAA | C | 9 | a0001c0001t0001g0049a0001c0001t0001g0073a0001c0001t0001g0096others(6): Show | 9 | HG00280.hp1 HG01515.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+1490_145+1493d others(6): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524644 | ||||||
| chr10:13524661
|
A | T | 7 | a0001c0001t0002g0246a0001c0003t0002g0247a0001c0003t0002g0249others(4): Show | 7 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.145+1477T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524661 | ||||||
| chr10:13524733
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.145+1405G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524733 | ||||||
| chr10:13524991
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(126): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.145+1147G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13524991 | ||||||
| chr10:13525134
|
G | A | 6 | a0001c0001t0005g0022a0001c0003t0005g0017a0001c0003t0005g0018others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+1004C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525134 | ||||||
| chr10:13525136
|
G | A | 3 | a0002c0005t0002g0243a0002c0005t0002g0244a0002c0005t0002g0245 | 3 | HG01891.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.145+1002C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525136 | ||||||
| chr10:13525158
|
T | C | 1 | a0001c0001t0010g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.145+980A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525158 | ||||||
| chr10:13525200
|
G | A | 1 | a0001c0001t0001g0008 | 2 | HG01109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.145+938C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525200 | ||||||
| chr10:13525261
|
G | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.145+877C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525261 | ||||||
| chr10:13525306
|
T | A | 2 | a0001c0002t0001g0012a0001c0002t0001g0190 | 3 | NA18747.hp2 NA18975.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.145+832A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525306 | ||||||
| chr10:13525306
|
T | C | 1 | a0001c0002t0001g0189 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.145+832A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525306 | ||||||
| chr10:13525318
|
C | T | 5 | a0001c0001t0001g0045a0001c0001t0006g0044a0001c0001t0006g0046others(2): Show | 5 | HG02602.hp1 HG03704.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+820G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525318 | ||||||
| chr10:13525343
|
G | A | 16 | a0001c0001t0004g0116a0001c0002t0001g0103a0001c0003t0001g0101others(13): Show | 16 | HG00639.hp2 HG01081.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+795C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525343 | ||||||
| chr10:13525362
|
A | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG01361.hp1 HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.145+776T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525362 | ||||||
| chr10:13525440
|
A | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(168): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.145+698T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525440 | ||||||
| chr10:13525617
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.145+521A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525617 | ||||||
| chr10:13525927
|
A | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(133): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.145+211T>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 2/8 | chr10 | 13525927 | ||||||
| chr10:13526226
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG04115.hp2 | splice_region_variant&intron_variant | LOW | c.62-5G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13526226 | ||||||
| chr10:13526794
|
T | C | 1 | a0001c0001t0006g0048 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.62-573A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13526794 | ||||||
| chr10:13526857
|
T | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(132): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.62-636A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13526857 | ||||||
| chr10:13526940
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(132): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.62-719G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13526940 | ||||||
| chr10:13526993
|
G | T | 14 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(11): Show | 14 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.62-772C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13526993 | ||||||
| chr10:13527004
|
G | C | 1 | a0001c0001t0002g0268 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.62-783C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527004 | ||||||
| chr10:13527226
|
G | GA | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.62-1006dupT | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527226 | ||||||
| chr10:13527265
|
T | C | 14 | a0001c0001t0001g0095a0001c0001t0003g0026a0001c0001t0003g0027others(11): Show | 14 | HG02602.hp2 HG02735.hp2 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.62-1044A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527265 | ||||||
| chr10:13527267
|
T | C | 35 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(32): Show | 38 | HG00639.hp2 HG01081.hp2 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.62-1046A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527267 | ||||||
| chr10:13527334
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 5 | HG02486.hp1 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-1113T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527334 | ||||||
| chr10:13527512
|
T | C | 1 | a0001c0001t0002g0241 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.61+961A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527512 | ||||||
| chr10:13527689
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.61+784T>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527689 | ||||||
| chr10:13527726
|
T | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.61+747A>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527726 | ||||||
| chr10:13527727
|
A | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.61+746T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527727 | ||||||
| chr10:13527728
|
A | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(119): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.61+745T>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527728 | ||||||
| chr10:13527805
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(132): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.61+668G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527805 | ||||||
| chr10:13527927
|
T | C | 13 | a0001c0003t0001g0005a0001c0003t0001g0120a0001c0003t0001g0121others(10): Show | 15 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+546A>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13527927 | ||||||
| chr10:13528066
|
C | T | 2 | a0001c0003t0001g0042a0001c0003t0001g0043 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.61+407G>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13528066 | ||||||
| chr10:13528085
|
G | T | 1 | a0001c0001t0001g0131 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.61+388C>A | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13528085 | ||||||
| chr10:13528312
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(142): Show | 159 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.61+161C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13528312 | ||||||
| chr10:13528341
|
G | A | 1 | a0001c0004t0001g0238 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.61+132C>T | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13528341 | ||||||
| chr10:13528365
|
G | C | 1 | a0001c0002t0001g0239 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.61+108C>G | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13528365 | ||||||
| chr10:13528412
|
C | CCGCGGGC others(9): Show |
6 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 8 | NA18952.hp2 NA18997.hp1 NA18999.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+45_61+60dupCCCT others(12): Show |
BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13528412 | ||||||
| chr10:13528451
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.61+22G>C | BEND7 | ENSG00000165626.19 | transcript | ENST00000466271.3 | protein_coding | 1/8 | chr10 | 13528451 |