Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55814 |
|---|---|
| ensemblid | ENSG00000145734.20 |
| hgncid | 13652 |
| symbol | BDP1 |
| name | B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB |
| refseq_nuc | NM_018429.3 |
| refseq_prot | NP_060899.2 |
| ensembl_nuc | ENST00000358731.9 |
| ensembl_prot | ENSP00000351575.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 71455651 |
| end | 71567820 |
| strand | + |
| ver | v1.2 |
| region | chr5:71455651-71567820 |
| region5000 | chr5:71450651-71572820 |
| regionname0 | BDP1_chr5_71455651_71567820 |
| regionname5000 | BDP1_chr5_71450651_71572820 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 2624 | 88 | 4 | 15 | 55 | 1 | 13 | 40 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002 | 0/0 | 2624 | 75 | 6 | 13 | 49 | 2 | 5 | 38 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0003 | 0/0 | 2624 | 58 | 19 | 10 | 19 | 3 | 7 | 14 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0004 | 0/0 | 2624 | 11 | 3 | 3 | 3 | 0 | 2 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0005 | 0/0 | 2624 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0006 | 0/0 | 2624 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0007 | 0/0 | 2624 | 8 | 0 | 6 | 0 | 1 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0008 | 0/0 | 2624 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0009 | 0/0 | 2624 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0010 | 0/0 | 2624 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0011 | 0/1 | 2624 | 5 | 0 | 3 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0012 | 0/0 | 2624 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0013 | 0/0 | 2624 | 5 | 0 | 0 | 4 | 0 | 1 | 4 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0014 | 0/0 | 2624 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0015 | 0/0 | 2624 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0016 | 0/0 | 2624 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0017 | 0/0 | 2624 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0018 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0019 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0020 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0021 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0022 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0023 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0024 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0025 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0026 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0027 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0028 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0029 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0030 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0031 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0032 | 0/0 | 1589 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0033 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0034 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0035 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0036 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0037 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0038 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0039 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0040 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0041 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0042 | 0/0 | 2624 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| 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 | 7875 | 84 | 3 | 15 | 54 | 1 | 11 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0002 | 0/0 | 7875 | 73 | 6 | 13 | 47 | 2 | 5 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0003 | 0/0 | 7875 | 57 | 18 | 10 | 19 | 3 | 7 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0004 | 0/0 | 7875 | 11 | 3 | 3 | 3 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0005 | 0/0 | 7875 | 10 | 9 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0006 | 0/0 | 7875 | 8 | 0 | 6 | 0 | 1 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0007 | 0/0 | 7875 | 7 | 7 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0008 | 0/0 | 7875 | 6 | 5 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0009 | 0/0 | 7875 | 6 | 6 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0010 | 0/0 | 7875 | 5 | 4 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0011 | 0/1 | 7875 | 5 | 0 | 3 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0012 | 0/0 | 7875 | 5 | 5 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0013 | 0/0 | 7875 | 5 | 0 | 0 | 4 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0014 | 0/0 | 7875 | 2 | 1 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0015 | 0/0 | 7875 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0016 | 0/0 | 7875 | 2 | 0 | 0 | 0 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0017 | 0/0 | 7875 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0018 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0019 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0020 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0021 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0022 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0023 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0024 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0025 | 0/0 | 7868 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0026 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0027 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0028 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0029 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0030 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0031 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0032 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0033 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0034 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0035 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0036 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0037 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0038 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0039 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0040 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0041 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0042 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0043 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0044 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0045 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0046 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0047 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0048 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0049 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0050 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0051 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| c0052 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| 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 | 0/0 | 3163 | 146 | 34 | 27 | 61 | 5 | 19 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0002 | 0/0 | 3163 | 114 | 21 | 21 | 55 | 3 | 14 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0003 | 0/0 | 3163 | 19 | 5 | 2 | 11 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0004 | 0/0 | 3163 | 10 | 1 | 3 | 3 | 0 | 3 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0005 | 0/0 | 3163 | 7 | 0 | 0 | 7 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0006 | 0/0 | 3163 | 5 | 4 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0007 | 0/0 | 3156 | 4 | 4 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0008 | 0/0 | 3163 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0009 | 0/0 | 3163 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0010 | 0/0 | 3163 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0011 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0012 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0013 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0014 | 0/1 | 3163 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0015 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0016 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0017 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0018 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0019 | 0/0 | 3163 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0020 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0021 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0022 | 0/0 | 3163 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0023 | 0/0 | 3163 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| t0024 | 0/0 | 3163 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| 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 | 7875 | 84 | 3 | 15 | 54 | 1 | 11 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0021 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0022 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0026 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0030 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002c0002 | 0/0 | 7875 | 73 | 6 | 13 | 47 | 2 | 5 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002c0039 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002c0041 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0003c0003 | 0/0 | 7875 | 57 | 18 | 10 | 19 | 3 | 7 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0003c0049 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0004c0004 | 0/0 | 7875 | 11 | 3 | 3 | 3 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0005c0005 | 0/0 | 7875 | 10 | 9 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0006c0007 | 0/0 | 7875 | 7 | 7 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0006c0024 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0006c0028 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0007c0006 | 0/0 | 7875 | 8 | 0 | 6 | 0 | 1 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0008c0009 | 0/0 | 7875 | 6 | 6 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0008c0048 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0009c0008 | 0/0 | 7875 | 6 | 5 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0010c0012 | 0/0 | 7875 | 5 | 5 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0011c0011 | 0/1 | 7875 | 5 | 0 | 3 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0012c0010 | 0/0 | 7875 | 5 | 4 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0013c0013 | 0/0 | 7875 | 5 | 0 | 0 | 4 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0014c0015 | 0/0 | 7875 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0015c0016 | 0/0 | 7875 | 2 | 0 | 0 | 0 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0016c0014 | 0/0 | 7875 | 2 | 1 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0017c0017 | 0/0 | 7875 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0018c0051 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0019c0050 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0020c0018 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0021c0020 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0022c0019 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0023c0046 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0024c0042 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0025c0038 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0026c0040 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0027c0037 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0028c0043 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0029c0044 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0030c0036 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0031c0029 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0032c0025 | 0/0 | 7868 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0033c0027 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0034c0023 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0035c0032 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0036c0034 | 0/0 | 7875 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0037c0033 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0038c0035 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0039c0031 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0040c0045 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0041c0047 | 0/0 | 7875 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0042c0052 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 11037 | 80 | 3 | 14 | 52 | 1 | 10 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0001t0011 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0001t0019 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0001t0020 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0001t0022 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0021t0002 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0022t0002 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0026t0002 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0001c0030t0002 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002c0002t0001 | 0/0 | 11037 | 55 | 6 | 11 | 31 | 2 | 5 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002c0002t0003 | 0/0 | 11037 | 11 | 0 | 1 | 10 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002c0002t0005 | 0/0 | 11037 | 6 | 0 | 0 | 6 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002c0002t0012 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002c0039t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0002c0041t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0003c0003t0001 | 0/0 | 11037 | 52 | 14 | 10 | 18 | 3 | 7 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0003c0003t0006 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0003c0003t0008 | 0/0 | 11037 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0003c0003t0013 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0003c0003t0018 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0003c0049t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0004c0004t0004 | 0/0 | 11037 | 9 | 1 | 3 | 3 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0004c0004t0010 | 0/0 | 11037 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0005c0005t0001 | 0/0 | 11037 | 8 | 8 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0005c0005t0015 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0005c0005t0017 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0006c0007t0002 | 0/0 | 11037 | 7 | 7 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0006c0024t0002 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0006c0028t0021 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0007c0006t0002 | 0/0 | 11037 | 8 | 0 | 6 | 0 | 1 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0008c0009t0002 | 0/0 | 11037 | 6 | 6 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0008c0048t0002 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0009c0008t0002 | 0/0 | 11037 | 2 | 1 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0009c0008t0007 | 0/0 | 11030 | 4 | 4 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0010c0012t0003 | 0/0 | 11037 | 5 | 5 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0011c0011t0001 | 0/0 | 11037 | 4 | 0 | 3 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0011c0011t0014 | 0/1 | 11037 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0012c0010t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0012c0010t0006 | 0/0 | 11037 | 4 | 3 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0013c0013t0001 | 0/0 | 11037 | 5 | 0 | 0 | 4 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0014c0015t0001 | 0/0 | 11037 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0015c0016t0001 | 0/0 | 11037 | 2 | 0 | 0 | 0 | 0 | 2 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0016c0014t0001 | 0/0 | 11037 | 2 | 1 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0017c0017t0009 | 0/0 | 11037 | 2 | 2 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0018c0051t0001 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0019c0050t0001 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0020c0018t0001 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0021c0020t0023 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0022c0019t0024 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0023c0046t0002 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0024c0042t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0025c0038t0001 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0026c0040t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0027c0037t0003 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0028c0043t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0029c0044t0005 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0030c0036t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0031c0029t0004 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0032c0025t0002 | 0/0 | 11030 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0033c0027t0002 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0034c0023t0002 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0035c0032t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0036c0034t0003 | 0/0 | 11037 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0037c0033t0003 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0038c0035t0001 | 0/0 | 11037 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0039c0031t0016 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0040c0045t0002 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0041c0047t0001 | 0/0 | 11037 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| a0042c0052t0001 | 0/0 | 11037 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | copy fasta | chr5 | 71450651 | 71572820 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0019g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0020g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0001t0022g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0021t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0022t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0026t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0001c0030t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0002t0012g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0039t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0002c0041t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0013g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0003t0018g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0003c0049t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0010g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0004c0004t0010g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0015g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0005c0005t0017g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0007t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0024t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0006c0028t0021g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0007c0006t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0009t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0008c0048t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0009c0008t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0012t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0012t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0012t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0012t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0010c0012t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0011t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0011t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0011t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0011t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0011c0011t0014g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0010t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0010t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0010t0006g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0010t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0012c0010t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0013c0013t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0013c0013t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0013c0013t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0013c0013t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0014c0015t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0014c0015t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0015c0016t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0015c0016t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0016c0014t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0016c0014t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0017c0017t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0017c0017t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0018c0051t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0019c0050t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0020c0018t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0021c0020t0023g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0022c0019t0024g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0023c0046t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0024c0042t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0025c0038t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0026c0040t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0027c0037t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0028c0043t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0029c0044t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0030c0036t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0031c0029t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0032c0025t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0033c0027t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0034c0023t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0035c0032t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0036c0034t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0037c0033t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0038c0035t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0039c0031t0016g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0040c0045t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0041c0047t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| a0042c0052t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0257 | EUR | GBR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00099 | hp2 | a0023 | c0046 | t0002 | g0027 | EUR | GBR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0261 | EUR | GBR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0295 | EUR | GBR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0151 | EUR | FIN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00280 | hp2 | a0007 | c0006 | t0002 | g0045 | EUR | FIN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0188 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00438 | hp1 | a0002 | c0002 | t0003 | g0212 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0282 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00609 | hp1 | a0002 | c0002 | t0003 | g0175 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00621 | hp1 | a0024 | c0042 | t0001 | g0182 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00642 | hp1 | a0011 | c0011 | t0001 | g0173 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00642 | hp2 | a0021 | c0020 | t0023 | g0119 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00733 | hp1 | a0016 | c0014 | t0001 | g0005 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0174 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00741 | hp1 | a0005 | c0005 | t0015 | g0310 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG00741 | hp2 | a0012 | c0010 | t0006 | g0250 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01069 | hp1 | a0007 | c0006 | t0002 | g0047 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0260 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0290 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0291 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01071 | hp2 | a0007 | c0006 | t0002 | g0046 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0272 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0259 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01167 | hp1 | a0009 | c0008 | t0002 | g0007 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0201 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0052 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01192 | hp1 | a0007 | c0006 | t0002 | g0079 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01192 | hp2 | a0003 | c0003 | t0001 | g0264 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01243 | hp2 | a0038 | c0035 | t0001 | g0123 | AMR | PUR | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0256 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01257 | hp1 | a0007 | c0006 | t0002 | g0044 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0262 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0258 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01433 | hp1 | a0004 | c0004 | t0004 | g0316 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01496 | hp2 | a0002 | c0002 | t0012 | g0157 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01884 | hp1 | a0039 | c0031 | t0016 | g0010 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01884 | hp2 | a0005 | c0005 | t0001 | g0237 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01943 | hp1 | a0004 | c0004 | t0004 | g0313 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01975 | hp1 | a0011 | c0011 | t0001 | g0185 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01978 | hp1 | a0020 | c0018 | t0001 | g0191 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01978 | hp2 | a0004 | c0004 | t0004 | g0312 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01981 | hp1 | a0011 | c0011 | t0001 | g0184 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0284 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02027 | hp1 | a0004 | c0004 | t0004 | g0311 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02027 | hp2 | a0002 | c0039 | t0001 | g0207 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02055 | hp1 | a0003 | c0003 | t0018 | g0307 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0305 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0283 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02071 | hp2 | a0001 | c0001 | t0022 | g0013 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02080 | hp1 | a0037 | c0033 | t0003 | g0137 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02148 | hp1 | a0007 | c0006 | t0002 | g0042 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0197 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0244 | EAS | CDX | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02257 | hp1 | a0035 | c0032 | t0001 | g0114 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02258 | hp1 | a0022 | c0019 | t0024 | g0118 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02258 | hp2 | a0012 | c0010 | t0006 | g0242 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02280 | hp2 | a0010 | c0012 | t0003 | g0204 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02300 | hp1 | a0027 | c0037 | t0003 | g0205 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02451 | hp1 | a0010 | c0012 | t0003 | g0166 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02451 | hp2 | a0005 | c0005 | t0001 | g0298 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0247 | EAS | KHV | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0216 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02572 | hp2 | a0008 | c0009 | t0002 | g0113 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02602 | hp1 | a0019 | c0050 | t0001 | g0288 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02602 | hp2 | a0015 | c0016 | t0001 | g0193 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02615 | hp1 | a0012 | c0010 | t0001 | g0239 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02615 | hp2 | a0003 | c0003 | t0006 | g0241 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02622 | hp1 | a0017 | c0017 | t0009 | g0116 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0281 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02683 | hp1 | a0015 | c0016 | t0001 | g0192 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02683 | hp2 | a0018 | c0051 | t0001 | g0263 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02735 | hp1 | a0025 | c0038 | t0001 | g0141 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02735 | hp2 | a0033 | c0027 | t0002 | g0011 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02738 | hp1 | a0003 | c0003 | t0001 | g0292 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0285 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02809 | hp2 | a0005 | c0005 | t0001 | g0299 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02886 | hp1 | a0005 | c0005 | t0017 | g0297 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0240 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02895 | hp1 | a0005 | c0005 | t0001 | g0296 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02895 | hp2 | a0006 | c0007 | t0002 | g0006 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02896 | hp1 | a0005 | c0005 | t0001 | g0235 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02896 | hp2 | a0006 | c0024 | t0002 | g0104 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02922 | hp1 | a0010 | c0012 | t0003 | g0165 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02922 | hp2 | a0008 | c0048 | t0002 | g0009 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02965 | hp1 | a0003 | c0003 | t0008 | g0279 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02965 | hp2 | a0006 | c0028 | t0021 | g0008 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02970 | hp1 | a0008 | c0009 | t0002 | g0111 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02970 | hp2 | a0003 | c0003 | t0008 | g0277 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02976 | hp1 | a0009 | c0008 | t0007 | g0095 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0278 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0248 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03041 | hp1 | a0006 | c0007 | t0002 | g0105 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0232 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03098 | hp1 | a0009 | c0008 | t0002 | g0090 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03098 | hp2 | a0012 | c0010 | t0006 | g0309 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03130 | hp1 | a0006 | c0007 | t0002 | g0107 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03130 | hp2 | a0041 | c0047 | t0001 | g0228 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03139 | hp1 | a0008 | c0009 | t0002 | g0112 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03139 | hp2 | a0010 | c0012 | t0003 | g0148 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03195 | hp1 | a0008 | c0009 | t0002 | g0028 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0286 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03209 | hp1 | a0006 | c0007 | t0002 | g0108 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0275 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0167 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03225 | hp2 | a0009 | c0008 | t0007 | g0097 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0186 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03239 | hp2 | a0001 | c0021 | t0002 | g0054 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03453 | hp2 | a0016 | c0014 | t0001 | g0004 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03486 | hp1 | a0004 | c0004 | t0010 | g0321 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03486 | hp2 | a0006 | c0007 | t0002 | g0103 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03490 | hp1 | a0011 | c0011 | t0001 | g0202 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0293 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0294 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03516 | hp1 | a0006 | c0007 | t0002 | g0109 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03516 | hp2 | a0012 | c0010 | t0006 | g0306 | AFR | ESN | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03540 | hp1 | a0017 | c0017 | t0009 | g0115 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03540 | hp2 | a0005 | c0005 | t0001 | g0234 | AFR | GWD | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03579 | hp1 | a0009 | c0008 | t0007 | g0098 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0255 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03669 | hp2 | a0031 | c0029 | t0004 | g0317 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03710 | hp2 | a0004 | c0004 | t0004 | g0315 | SAS | PJL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03927 | hp2 | a0013 | c0013 | t0001 | g0143 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03942 | hp1 | a0001 | c0022 | t0002 | g0081 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03942 | hp2 | a0001 | c0001 | t0019 | g0016 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04184 | hp1 | a0036 | c0034 | t0003 | g0138 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04184 | hp2 | a0007 | c0006 | t0002 | g0043 | SAS | BEB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04199 | hp1 | a0004 | c0004 | t0004 | g0314 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0268 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0140 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0271 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0265 | SAS | STU | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0230 | EAS | CHB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18906 | hp1 | a0005 | c0005 | t0001 | g0233 | AFR | YRI | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0276 | AFR | YRI | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18939 | hp2 | a0026 | c0040 | t0001 | g0152 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0238 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18943 | hp1 | a0003 | c0003 | t0013 | g0251 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18948 | hp2 | a0003 | c0003 | t0001 | g0245 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0161 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0169 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18957 | hp2 | a0002 | c0041 | t0001 | g0144 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0249 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18959 | hp2 | a0002 | c0002 | t0005 | g0183 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18963 | hp1 | a0002 | c0002 | t0005 | g0189 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18966 | hp1 | a0001 | c0030 | t0002 | g0031 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0267 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18974 | hp1 | a0014 | c0015 | t0001 | g0221 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18978 | hp2 | a0002 | c0002 | t0005 | g0215 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0270 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0179 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18982 | hp2 | a0034 | c0023 | t0002 | g0069 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0243 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18984 | hp1 | a0030 | c0036 | t0001 | g0149 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18985 | hp2 | a0003 | c0003 | t0001 | g0253 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18989 | hp2 | a0013 | c0013 | t0001 | g0133 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18991 | hp2 | a0002 | c0002 | t0005 | g0178 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0162 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0254 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18998 | hp2 | a0029 | c0044 | t0005 | g0194 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA18999 | hp2 | a0002 | c0002 | t0005 | g0300 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19004 | hp1 | a0013 | c0013 | t0001 | g0003 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19006 | hp2 | a0002 | c0002 | t0003 | g0134 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19030 | hp1 | a0040 | c0045 | t0002 | g0091 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19043 | hp1 | a0009 | c0008 | t0007 | g0096 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0274 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19054 | hp1 | a0013 | c0013 | t0001 | g0217 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19054 | hp2 | a0001 | c0001 | t0011 | g0061 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19055 | hp1 | a0003 | c0003 | t0001 | g0287 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19063 | hp1 | a0002 | c0002 | t0005 | g0171 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19064 | hp1 | a0014 | c0015 | t0001 | g0223 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19068 | hp1 | a0002 | c0002 | t0003 | g0206 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19070 | hp1 | a0042 | c0052 | t0001 | g0226 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0273 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19082 | hp1 | a0004 | c0004 | t0004 | g0319 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19084 | hp1 | a0003 | c0003 | t0001 | g0252 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19086 | hp2 | a0003 | c0003 | t0001 | g0266 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19087 | hp1 | a0004 | c0004 | t0004 | g0320 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0246 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19088 | hp2 | a0013 | c0013 | t0001 | g0003 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0177 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19091 | hp1 | a0032 | c0025 | t0002 | g0066 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20129 | hp1 | a0004 | c0004 | t0010 | g0322 | AFR | ASW | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20129 | hp2 | a0008 | c0009 | t0002 | g0053 | AFR | ASW | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | TSI | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0203 | EUR | TSI | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01123 | hp1 | a0007 | c0006 | t0002 | g0017 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | CLM | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02109 | hp2 | a0028 | c0043 | t0001 | g0139 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02486 | hp1 | a0010 | c0012 | t0003 | g0209 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0308 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02559 | hp1 | a0003 | c0049 | t0001 | g0269 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG02559 | hp2 | a0005 | c0005 | t0001 | g0236 | AFR | ACB | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03471 | hp1 | a0008 | c0009 | t0002 | g0110 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0280 | AFR | MSL | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG06807 | hp1 | a0004 | c0004 | t0004 | g0318 | AFR | USA | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | USA | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | USA | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA20300 | hp2 | a0006 | c0007 | t0002 | g0106 | AFR | USA | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA21309 | hp1 | a0001 | c0026 | t0002 | g0012 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0231 | AFR | LWK | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| homoSapiens_chm13v2 | hp1 | a0011 | c0011 | t0014 | g0147 | REF | REF | BDP1_chr5_71450651_71572820 | BDP1 | chr5 | 71450651 | 71572820 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71455954
|
A | G | 1 | a0042 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.77A>G | p.Asn26Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 304/11037 | 77/7875 | 26/2624 | chr5 | 71455954 | ||
| chr5:71455991
|
T | G | 37 | a0001a0002a0004others(34): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
missense_variant | MODERATE | c.114T>G | p.Asp38Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 341/11037 | 114/7875 | 38/2624 | chr5 | 71455991 | ||
| chr5:71458621
|
T | G | 1 | a0020 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.255T>G | p.Ser85Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/39 | 482/11037 | 255/7875 | 85/2624 | chr5 | 71458621 | ||
| chr5:71458648
|
A | T | 1 | a0013 | 5 | HG03927.hp2 NA18989.hp2 NA19004.hp1 others(2): Show |
missense_variant | MODERATE | c.282A>T | p.Arg94Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/39 | 509/11037 | 282/7875 | 94/2624 | chr5 | 71458648 | ||
| chr5:71458740
|
C | T | 1 | a0009 | 6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
missense_variant | MODERATE | c.374C>T | p.Ala125Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/39 | 601/11037 | 374/7875 | 125/2624 | chr5 | 71458740 | ||
| chr5:71467391
|
G | A | 2 | a0021a0022 | 2 | HG00642.hp2 HG02258.hp1 |
missense_variant | MODERATE | c.823G>A | p.Val275Ile | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/39 | 1050/11037 | 823/7875 | 275/2624 | chr5 | 71467391 | ||
| chr5:71491003
|
G | T | 2 | a0017a0041 | 3 | HG02622.hp1 HG03130.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.1512G>T | p.Arg504Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/39 | 1739/11037 | 1512/7875 | 504/2624 | chr5 | 71491003 | ||
| chr5:71502714
|
A | G | 2 | a0007a0023 | 9 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(6): Show |
missense_variant | MODERATE | c.2164A>G | p.Lys722Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/39 | 2391/11037 | 2164/7875 | 722/2624 | chr5 | 71502714 | ||
| chr5:71502726
|
A | T | 1 | a0040 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2176A>T | p.Ile726Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/39 | 2403/11037 | 2176/7875 | 726/2624 | chr5 | 71502726 | ||
| chr5:71504648
|
C | T | 15 | a0002a0010a0011others(12): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
missense_variant | MODERATE | c.2269C>T | p.Arg757Cys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/39 | 2496/11037 | 2269/7875 | 757/2624 | chr5 | 71504648 | ||
| chr5:71504711
|
G | A | 12 | a0001a0004a0006others(9): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
missense_variant | MODERATE | c.2332G>A | p.Val778Met | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/39 | 2559/11037 | 2332/7875 | 778/2624 | chr5 | 71504711 | ||
| chr5:71509484
|
G | T | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2392G>T | p.Ala798Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2619/11037 | 2392/7875 | 798/2624 | chr5 | 71509484 | ||
| chr5:71509491
|
A | G | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2399A>G | p.Lys800Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2626/11037 | 2399/7875 | 800/2624 | chr5 | 71509491 | ||
| chr5:71509494
|
T | C | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2402T>C | p.Leu801Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2629/11037 | 2402/7875 | 801/2624 | chr5 | 71509494 | ||
| chr5:71509498
|
C | G | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2406C>G | p.Asn802Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2633/11037 | 2406/7875 | 802/2624 | chr5 | 71509498 | ||
| chr5:71509499
|
C | A | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2407C>A | p.Gln803Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2634/11037 | 2407/7875 | 803/2624 | chr5 | 71509499 | ||
| chr5:71509502
|
G | T | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2410G>T | p.Val804Phe | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2637/11037 | 2410/7875 | 804/2624 | chr5 | 71509502 | ||
| chr5:71509503
|
T | A | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2411T>A | p.Val804Asp | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2638/11037 | 2411/7875 | 804/2624 | chr5 | 71509503 | ||
| chr5:71509509
|
T | G | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2417T>G | p.Ile806Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2644/11037 | 2417/7875 | 806/2624 | chr5 | 71509509 | ||
| chr5:71509512
|
T | G | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2420T>G | p.Leu807Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2647/11037 | 2420/7875 | 807/2624 | chr5 | 71509512 | ||
| chr5:71509515
|
G | C | 1 | a0030 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.2423G>C | p.Arg808Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2650/11037 | 2423/7875 | 808/2624 | chr5 | 71509515 | ||
| chr5:71510016
|
A | T | 1 | a0029 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.2924A>T | p.Asp975Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3151/11037 | 2924/7875 | 975/2624 | chr5 | 71510016 | ||
| chr5:71510135
|
A | C | 1 | a0021 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.3043A>C | p.Thr1015Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3270/11037 | 3043/7875 | 1015/2624 | chr5 | 71510135 | ||
| chr5:71510157
|
G | A | 1 | a0041 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.3065G>A | p.Arg1022Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3292/11037 | 3065/7875 | 1022/2624 | chr5 | 71510157 | ||
| chr5:71510304
|
G | C | 1 | a0017 | 2 | HG02622.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.3212G>C | p.Ser1071Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3439/11037 | 3212/7875 | 1071/2624 | chr5 | 71510304 | ||
| chr5:71510360
|
G | T | 1 | a0028 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3268G>T | p.Asp1090Tyr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3495/11037 | 3268/7875 | 1090/2624 | chr5 | 71510360 | ||
| chr5:71510399
|
A | G | 1 | a0031 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3307A>G | p.Asn1103Asp | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3534/11037 | 3307/7875 | 1103/2624 | chr5 | 71510399 | ||
| chr5:71510456
|
G | A | 1 | a0023 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.3364G>A | p.Gly1122Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3591/11037 | 3364/7875 | 1122/2624 | chr5 | 71510456 | ||
| chr5:71510630
|
G | A | 13 | a0001a0004a0006others(10): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
missense_variant | MODERATE | c.3538G>A | p.Gly1180Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3765/11037 | 3538/7875 | 1180/2624 | chr5 | 71510630 | ||
| chr5:71510694
|
A | C | 1 | a0018 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.3602A>C | p.Glu1201Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3829/11037 | 3602/7875 | 1201/2624 | chr5 | 71510694 | ||
| chr5:71510780
|
A | G | 1 | a0038 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.3688A>G | p.Ile1230Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3915/11037 | 3688/7875 | 1230/2624 | chr5 | 71510780 | ||
| chr5:71510810
|
G | T | 1 | a0024 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.3718G>T | p.Val1240Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3945/11037 | 3718/7875 | 1240/2624 | chr5 | 71510810 | ||
| chr5:71510822
|
T | A | 13 | a0001a0004a0006others(10): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
missense_variant | MODERATE | c.3730T>A | p.Phe1244Ile | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3957/11037 | 3730/7875 | 1244/2624 | chr5 | 71510822 | ||
| chr5:71510884
|
C | G | 36 | a0001a0002a0004others(33): Show | 249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
missense_variant | MODERATE | c.3792C>G | p.Ile1264Met | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 4019/11037 | 3792/7875 | 1264/2624 | chr5 | 71510884 | ||
| chr5:71510931
|
C | G | 1 | a0015 | 2 | HG02602.hp2 HG02683.hp1 |
missense_variant | MODERATE | c.3839C>G | p.Ala1280Gly | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 4066/11037 | 3839/7875 | 1280/2624 | chr5 | 71510931 | ||
| chr5:71511131
|
G | A | 36 | a0001a0002a0004others(33): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
missense_variant | MODERATE | c.4039G>A | p.Val1347Met | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 4266/11037 | 4039/7875 | 1347/2624 | chr5 | 71511131 | ||
| chr5:71512419
|
T | C | 1 | a0034 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.4238T>C | p.Ile1413Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/39 | 4465/11037 | 4238/7875 | 1413/2624 | chr5 | 71512419 | ||
| chr5:71513342
|
A | G | 10 | a0001a0006a0007others(7): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
missense_variant | MODERATE | c.4405A>G | p.Lys1469Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/39 | 4632/11037 | 4405/7875 | 1469/2624 | chr5 | 71513342 | ||
| chr5:71515109
|
G | T | 1 | a0022 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.4636G>T | p.Val1546Phe | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/39 | 4863/11037 | 4636/7875 | 1546/2624 | chr5 | 71515109 | ||
| chr5:71516170
|
GGACAGAG others(10): Show |
G | 1 | a0032 | 1 | NA19091.hp1 | frameshift_variant | HIGH | c.4764_4780delGAGGCA others(11): Show |
p.Gln1590fs | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/39 | 4991/11037 | 4764/7875 | 1588/2624 | INFO_REALIGN_3_PRIME | chr5 | 71516170 | |
| chr5:71516213
|
T | G | 1 | a0032 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.4802T>G | p.Ile1601Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/39 | 5029/11037 | 4802/7875 | 1601/2624 | chr5 | 71516213 | ||
| chr5:71516218
|
G | GCAAGGAT others(3): Show |
1 | a0032 | 1 | NA19091.hp1 | frameshift_variant | HIGH | c.4807_4808insCAAGGA others(4): Show |
p.Glu1603fs | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/39 | 5035/11037 | 4808/7875 | 1603/2624 | chr5 | 71516218 | ||
| chr5:71522303
|
C | A | 2 | a0004a0031 | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
missense_variant | MODERATE | c.5006C>A | p.Pro1669Gln | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/39 | 5233/11037 | 5006/7875 | 1669/2624 | chr5 | 71522303 | ||
| chr5:71522323
|
C | G | 1 | a0010 | 5 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
missense_variant | MODERATE | c.5026C>G | p.Gln1676Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/39 | 5253/11037 | 5026/7875 | 1676/2624 | chr5 | 71522323 | ||
| chr5:71522328
|
G | C | 2 | a0035a0038 | 2 | HG01243.hp2 HG02257.hp1 |
missense_variant | MODERATE | c.5031G>C | p.Met1677Ile | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/39 | 5258/11037 | 5031/7875 | 1677/2624 | chr5 | 71522328 | ||
| chr5:71522774
|
A | C | 1 | a0036 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.5212A>C | p.Thr1738Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/39 | 5439/11037 | 5212/7875 | 1738/2624 | chr5 | 71522774 | ||
| chr5:71524099
|
C | T | 1 | a0019 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.5548C>T | p.Arg1850Trp | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/39 | 5775/11037 | 5548/7875 | 1850/2624 | chr5 | 71524099 | ||
| chr5:71541468
|
A | C | 38 | a0001a0002a0004others(35): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
missense_variant | MODERATE | c.6037A>C | p.Ile2013Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 29/39 | 6264/11037 | 6037/7875 | 2013/2624 | chr5 | 71541468 | ||
| chr5:71542154
|
G | A | 1 | a0014 | 2 | NA18974.hp1 NA19064.hp1 |
missense_variant | MODERATE | c.6301G>A | p.Ala2101Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/39 | 6528/11037 | 6301/7875 | 2101/2624 | chr5 | 71542154 | ||
| chr5:71545076
|
A | G | 1 | a0022 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.6601A>G | p.Met2201Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/39 | 6828/11037 | 6601/7875 | 2201/2624 | chr5 | 71545076 | ||
| chr5:71548685
|
A | G | 1 | a0039 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.6748A>G | p.Thr2250Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/39 | 6975/11037 | 6748/7875 | 2250/2624 | chr5 | 71548685 | ||
| chr5:71548691
|
A | C | 1 | a0022 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.6754A>C | p.Thr2252Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/39 | 6981/11037 | 6754/7875 | 2252/2624 | chr5 | 71548691 | ||
| chr5:71549573
|
A | G | 1 | a0006 | 9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
missense_variant | MODERATE | c.6962A>G | p.Lys2321Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/39 | 7189/11037 | 6962/7875 | 2321/2624 | chr5 | 71549573 | ||
| chr5:71553120
|
T | C | 1 | a0027 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.7000T>C | p.Cys2334Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7227/11037 | 7000/7875 | 2334/2624 | chr5 | 71553120 | ||
| chr5:71553142
|
G | T | 1 | a0026 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.7022G>T | p.Gly2341Val | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7249/11037 | 7022/7875 | 2341/2624 | chr5 | 71553142 | ||
| chr5:71553309
|
T | G | 1 | a0013 | 5 | HG03927.hp2 NA18989.hp2 NA19004.hp1 others(2): Show |
missense_variant | MODERATE | c.7189T>G | p.Tyr2397Asp | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7416/11037 | 7189/7875 | 2397/2624 | chr5 | 71553309 | ||
| chr5:71560035
|
A | G | 1 | a0033 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.7294A>G | p.Thr2432Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/39 | 7521/11037 | 7294/7875 | 2432/2624 | chr5 | 71560035 | ||
| chr5:71562441
|
A | G | 2 | a0020a0025 | 2 | HG01978.hp1 HG02735.hp1 |
missense_variant | MODERATE | c.7664A>G | p.Asn2555Ser | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/39 | 7891/11037 | 7664/7875 | 2555/2624 | chr5 | 71562441 | ||
| chr5:71562515
|
A | G | 1 | a0011 | 5 | HG00642.hp1 HG01975.hp1 HG01981.hp1 others(2): Show |
missense_variant | MODERATE | c.7738A>G | p.Thr2580Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/39 | 7965/11037 | 7738/7875 | 2580/2624 | chr5 | 71562515 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71502698
|
T | A | 1 | a0001c0021 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.2148T>A | p.Gly716Gly | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/39 | 2375/11037 | 2148/7875 | 716/2624 | chr5 | 71502698 | ||
| chr5:71509474
|
G | A | 1 | a0030c0036 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.2382G>A | p.Glu794Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2609/11037 | 2382/7875 | 794/2624 | chr5 | 71509474 | ||
| chr5:71509480
|
T | C | 1 | a0030c0036 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.2388T>C | p.Asn796Asn | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2615/11037 | 2388/7875 | 796/2624 | chr5 | 71509480 | ||
| chr5:71509495
|
T | A | 1 | a0030c0036 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.2403T>A | p.Leu801Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2630/11037 | 2403/7875 | 801/2624 | chr5 | 71509495 | ||
| chr5:71509534
|
A | C | 1 | a0030c0036 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.2442A>C | p.Pro814Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2669/11037 | 2442/7875 | 814/2624 | chr5 | 71509534 | ||
| chr5:71509627
|
A | G | 1 | a0001c0030 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.2535A>G | p.Ala845Ala | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 2762/11037 | 2535/7875 | 845/2624 | chr5 | 71509627 | ||
| chr5:71510602
|
G | A | 1 | a0008c0048 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.3510G>A | p.Glu1170Glu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3737/11037 | 3510/7875 | 1170/2624 | chr5 | 71510602 | ||
| chr5:71510746
|
G | A | 1 | a0001c0022 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.3654G>A | p.Lys1218Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/39 | 3881/11037 | 3654/7875 | 1218/2624 | chr5 | 71510746 | ||
| chr5:71513209
|
G | A | 1 | a0006c0024 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.4272G>A | p.Lys1424Lys | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/39 | 4499/11037 | 4272/7875 | 1424/2624 | chr5 | 71513209 | ||
| chr5:71522929
|
A | G | 1 | a0006c0028 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.5367A>G | p.Gln1789Gln | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/39 | 5594/11037 | 5367/7875 | 1789/2624 | chr5 | 71522929 | ||
| chr5:71524101
|
G | T | 1 | a0002c0041 | 1 | NA18957.hp2 | synonymous_variant | LOW | c.5550G>T | p.Arg1850Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/39 | 5777/11037 | 5550/7875 | 1850/2624 | chr5 | 71524101 | ||
| chr5:71532319
|
T | G | 1 | a0016c0014 | 2 | HG00733.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.5784T>G | p.Thr1928Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/39 | 6011/11037 | 5784/7875 | 1928/2624 | chr5 | 71532319 | ||
| chr5:71532424
|
G | A | 1 | a0041c0047 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.5889G>A | p.Pro1963Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/39 | 6116/11037 | 5889/7875 | 1963/2624 | chr5 | 71532424 | ||
| chr5:71539065
|
C | A | 2 | a0004c0004a0031c0029 | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
synonymous_variant | LOW | c.5916C>A | p.Ile1972Ile | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/39 | 6143/11037 | 5916/7875 | 1972/2624 | chr5 | 71539065 | ||
| chr5:71544406
|
C | T | 16 | a0001c0001a0001c0021a0001c0022others(13): Show | 122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
synonymous_variant | LOW | c.6462C>T | p.Leu2154Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/39 | 6689/11037 | 6462/7875 | 2154/2624 | chr5 | 71544406 | ||
| chr5:71553134
|
T | G | 1 | a0003c0049 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.7014T>G | p.Thr2338Thr | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7241/11037 | 7014/7875 | 2338/2624 | chr5 | 71553134 | ||
| chr5:71553194
|
G | T | 19 | a0001c0001a0001c0021a0001c0022others(16): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
synonymous_variant | LOW | c.7074G>T | p.Pro2358Pro | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/39 | 7301/11037 | 7074/7875 | 2358/2624 | chr5 | 71553194 | ||
| chr5:71560232
|
A | G | 1 | a0002c0039 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.7491A>G | p.Leu2497Leu | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/39 | 7718/11037 | 7491/7875 | 2497/2624 | chr5 | 71560232 | ||
| chr5:71562367
|
C | T | 17 | a0002c0002a0002c0039a0002c0041others(14): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
synonymous_variant | LOW | c.7590C>T | p.Arg2530Arg | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/39 | 7817/11037 | 7590/7875 | 2530/2624 | chr5 | 71562367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71455691
|
A | G | 1 | a0004c0004t0010 | 2 | HG03486.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-187A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 187 | chr5 | 71455691 | |||||
| chr5:71455798
|
A | T | 3 | a0017c0017t0009a0021c0020t0023a0022c0019t0024 | 4 | HG00642.hp2 HG02258.hp1 HG02622.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-80A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 80 | chr5 | 71455798 | |||||
| chr5:71455820
|
C | A | 1 | a0001c0001t0011 | 1 | NA19054.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 58 | chr5 | 71455820 | |||||
| chr5:71455876
|
C | T | 1 | a0001c0001t0022 | 1 | HG02071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/39 | 2 | chr5 | 71455876 | |||||
| chr5:71565377
|
A | G | 1 | a0022c0019t0024 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*492A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 492 | chr5 | 71565377 | |||||
| chr5:71565662
|
G | A | 3 | a0004c0004t0004a0004c0004t0010a0031c0029t0004 | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*777G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 777 | chr5 | 71565662 | |||||
| chr5:71565925
|
A | G | 2 | a0002c0002t0005a0029c0044t0005 | 7 | NA18959.hp2 NA18963.hp1 NA18978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1040A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1040 | chr5 | 71565925 | |||||
| chr5:71565930
|
T | G | 3 | a0004c0004t0004a0004c0004t0010a0031c0029t0004 | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1045T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1045 | chr5 | 71565930 | |||||
| chr5:71566023
|
A | T | 2 | a0003c0003t0006a0012c0010t0006 | 5 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1138A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1138 | chr5 | 71566023 | |||||
| chr5:71566107
|
A | G | 1 | a0022c0019t0024 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1222A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1222 | chr5 | 71566107 | |||||
| chr5:71566127
|
A | T | 1 | a0021c0020t0023 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1242A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1242 | chr5 | 71566127 | |||||
| chr5:71566232
|
C | T | 25 | a0001c0001t0002a0001c0001t0011a0001c0001t0019others(22): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1347C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1347 | chr5 | 71566232 | |||||
| chr5:71566560
|
A | G | 1 | a0003c0003t0018 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1675A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1675 | chr5 | 71566560 | |||||
| chr5:71566620
|
C | T | 1 | a0003c0003t0008 | 2 | HG02965.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1735C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 1735 | chr5 | 71566620 | |||||
| chr5:71566910
|
T | C | 1 | a0022c0019t0024 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2025T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2025 | chr5 | 71566910 | |||||
| chr5:71566977
|
C | A | 1 | a0002c0002t0012 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2092C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2092 | chr5 | 71566977 | |||||
| chr5:71567047
|
C | T | 25 | a0001c0001t0002a0001c0001t0011a0001c0001t0019others(22): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2162C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2162 | chr5 | 71567047 | |||||
| chr5:71567052
|
C | T | 6 | a0002c0002t0003a0002c0002t0012a0010c0012t0003others(3): Show | 20 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2167C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2167 | chr5 | 71567052 | |||||
| chr5:71567264
|
C | T | 1 | a0005c0005t0017 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2379C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2379 | chr5 | 71567264 | |||||
| chr5:71567329
|
G | A | 1 | a0001c0001t0019 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2444G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2444 | chr5 | 71567329 | |||||
| chr5:71567402
|
A | G | 1 | a0006c0028t0021 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2517A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2517 | chr5 | 71567402 | |||||
| chr5:71567443
|
A | G | 1 | a0039c0031t0016 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2558A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2558 | chr5 | 71567443 | |||||
| chr5:71567532
|
AAGTTTTT | A | 1 | a0009c0008t0007 | 4 | HG02976.hp1 HG03225.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2649_*2655delGTTT others(3): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2649 | INFO_REALIGN_3_PRIME | chr5 | 71567532 | ||||
| chr5:71567605
|
C | T | 1 | a0001c0001t0020 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2720C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2720 | chr5 | 71567605 | |||||
| chr5:71567652
|
C | A | 1 | a0003c0003t0013 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2767C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2767 | chr5 | 71567652 | |||||
| chr5:71567654
|
A | G | 1 | a0005c0005t0015 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2769A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2769 | chr5 | 71567654 | |||||
| chr5:71567755
|
T | G | 1 | a0011c0011t0014 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2870T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2870 | chr5 | 71567755 | |||||
| chr5:71567775
|
G | T | 3 | a0004c0004t0004a0004c0004t0010a0031c0029t0004 | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2890G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2890 | chr5 | 71567775 | |||||
| chr5:71567789
|
T | A | 2 | a0017c0017t0009a0021c0020t0023 | 3 | HG00642.hp2 HG02622.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2904T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 39/39 | 2904 | chr5 | 71567789 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:71456153
|
C | G | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+64C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71456153 | ||||||
| chr5:71456941
|
C | A | 142 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(139): Show | 144 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.212+852C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71456941 | ||||||
| chr5:71456996
|
A | T | 8 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(5): Show | 8 | HG02056.hp2 NA18950.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.212+907A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71456996 | ||||||
| chr5:71457030
|
A | G | 1 | a0005c0005t0015g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.212+941A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457030 | ||||||
| chr5:71457059
|
T | G | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.212+970T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457059 | ||||||
| chr5:71457101
|
GTT | G | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+1013_212+1014d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457101 | ||||||
| chr5:71457195
|
G | C | 10 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(7): Show | 10 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.212+1106G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457195 | ||||||
| chr5:71457275
|
C | A | 1 | a0006c0007t0002g0006 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.212+1186C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457275 | ||||||
| chr5:71457307
|
G | GT | 16 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(13): Show | 16 | HG00438.hp2 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.212+1235dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr5 | 71457307 | |||||
| chr5:71457307
|
GT | G | 6 | a0002c0002t0001g0132a0006c0028t0021g0008a0008c0048t0002g0009others(3): Show | 6 | HG01167.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.212+1235delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr5 | 71457307 | |||||
| chr5:71457414
|
C | T | 1 | a0002c0002t0005g0300 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.213-1165C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457414 | ||||||
| chr5:71457418
|
C | G | 1 | a0005c0005t0001g0299 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.213-1161C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457418 | ||||||
| chr5:71457481
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.213-1098A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71457481 | ||||||
| chr5:71458107
|
G | A | 138 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(135): Show | 140 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.213-472G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458107 | ||||||
| chr5:71458335
|
G | C | 322 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(319): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.213-244G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458335 | ||||||
| chr5:71458370
|
TAA | T | 3 | a0005c0005t0001g0296a0005c0005t0001g0298a0005c0005t0017g0297 | 3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.213-208_213-207del others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458370 | ||||||
| chr5:71458371
|
A | G | 4 | a0008c0009t0002g0110a0008c0009t0002g0111a0008c0009t0002g0112others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.213-208A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458371 | ||||||
| chr5:71458429
|
C | T | 3 | a0005c0005t0001g0296a0005c0005t0001g0298a0005c0005t0017g0297 | 3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.213-150C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458429 | ||||||
| chr5:71458493
|
T | C | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.213-86T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 1/38 | chr5 | 71458493 | ||||||
| chr5:71459179
|
A | G | 2 | a0004c0004t0004g0319a0004c0004t0004g0320 | 2 | NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.489+324A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459179 | ||||||
| chr5:71459254
|
G | T | 6 | a0003c0003t0001g0290a0003c0003t0001g0291a0003c0003t0001g0292others(3): Show | 6 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+399G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459254 | ||||||
| chr5:71459318
|
C | T | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.489+463C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459318 | ||||||
| chr5:71459381
|
G | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489+526G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459381 | ||||||
| chr5:71459579
|
C | G | 7 | a0006c0007t0002g0103a0006c0007t0002g0105a0006c0007t0002g0106others(4): Show | 7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+724C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459579 | ||||||
| chr5:71459734
|
C | T | 1 | a0002c0002t0001g0289 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.489+879C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71459734 | ||||||
| chr5:71460026
|
A | G | 138 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(135): Show | 140 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.489+1171A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460026 | ||||||
| chr5:71460047
|
T | A | 2 | a0021c0020t0023g0119a0022c0019t0024g0118 | 2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.489+1192T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460047 | ||||||
| chr5:71460071
|
G | C | 2 | a0021c0020t0023g0119a0022c0019t0024g0118 | 2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.489+1216G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460071 | ||||||
| chr5:71460240
|
T | C | 248 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.489+1385T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460240 | ||||||
| chr5:71460252
|
C | T | 1 | a0002c0002t0001g0229 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.489+1397C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460252 | ||||||
| chr5:71460272
|
C | G | 1 | a0019c0050t0001g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.489+1417C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460272 | ||||||
| chr5:71460294
|
C | T | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.489+1439C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460294 | ||||||
| chr5:71460321
|
G | A | 1 | a0033c0027t0002g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.489+1466G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460321 | ||||||
| chr5:71460335
|
G | A | 2 | a0021c0020t0023g0119a0022c0019t0024g0118 | 2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.489+1480G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460335 | ||||||
| chr5:71460737
|
G | A | 1 | a0033c0027t0002g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490-1080G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460737 | ||||||
| chr5:71460763
|
G | A | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-1054G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71460763 | ||||||
| chr5:71460875
|
T | TA | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.490-933dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr5 | 71460875 | |||||
| chr5:71461131
|
C | T | 4 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0101others(1): Show | 4 | HG00621.hp2 NA18949.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-686C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461131 | ||||||
| chr5:71461193
|
A | T | 4 | a0009c0008t0007g0095a0009c0008t0007g0096a0009c0008t0007g0097others(1): Show | 4 | HG02976.hp1 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-624A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461193 | ||||||
| chr5:71461442
|
C | CA | 6 | a0001c0001t0002g0014a0001c0001t0002g0015a0002c0002t0001g0135others(3): Show | 6 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-362dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr5 | 71461442 | |||||
| chr5:71461456
|
C | A | 1 | a0001c0001t0022g0013 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.490-361C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461456 | ||||||
| chr5:71461530
|
C | T | 2 | a0006c0007t0002g0108a0006c0007t0002g0109 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.490-287C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461530 | ||||||
| chr5:71461605
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.490-212C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 2/38 | chr5 | 71461605 | ||||||
| chr5:71461958
|
C | CT | 208 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(205): Show | 211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.599+53dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71461958 | |||||
| chr5:71461958
|
C | CTT | 13 | a0001c0001t0002g0015a0001c0001t0002g0092a0001c0001t0002g0093others(10): Show | 13 | HG00673.hp1 HG02071.hp1 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.599+52_599+53dupTT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71461958 | |||||
| chr5:71461958
|
CT | C | 16 | a0003c0003t0001g0231a0004c0004t0004g0311a0004c0004t0004g0312others(13): Show | 16 | HG00642.hp2 HG01433.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.599+53delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71461958 | |||||
| chr5:71461960
|
T | C | 1 | a0003c0003t0001g0230 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.599+34T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71461960 | ||||||
| chr5:71462147
|
G | A | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.599+221G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462147 | ||||||
| chr5:71462272
|
A | G | 104 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(101): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.599+346A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462272 | ||||||
| chr5:71462643
|
A | G | 6 | a0002c0002t0001g0222a0002c0002t0001g0224a0002c0002t0001g0225others(3): Show | 6 | HG00673.hp1 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.599+717A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462643 | ||||||
| chr5:71462759
|
C | CA | 7 | a0001c0001t0019g0016a0002c0002t0001g0132a0002c0002t0001g0136others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.599+844dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71462759 | |||||
| chr5:71462859
|
G | A | 1 | a0007c0006t0002g0017 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.599+933G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462859 | ||||||
| chr5:71462990
|
G | A | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.599+1064G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71462990 | ||||||
| chr5:71463004
|
A | G | 6 | a0009c0008t0002g0007a0009c0008t0002g0090a0009c0008t0007g0095others(3): Show | 6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.600-1054A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463004 | ||||||
| chr5:71463396
|
G | A | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.600-662G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463396 | ||||||
| chr5:71463493
|
A | T | 101 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(98): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.600-565A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463493 | ||||||
| chr5:71463537
|
C | T | 5 | a0002c0002t0001g0218a0002c0002t0001g0219a0002c0002t0001g0220others(2): Show | 5 | HG02071.hp1 HG02074.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.600-521C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463537 | ||||||
| chr5:71463600
|
T | C | 4 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020others(1): Show | 4 | HG02015.hp2 NA18747.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.600-458T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463600 | ||||||
| chr5:71463609
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.600-449C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463609 | ||||||
| chr5:71463829
|
TA | T | 111 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(108): Show | 112 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.600-212delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71463829 | |||||
| chr5:71463829
|
TAA | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.600-213_600-212del others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr5 | 71463829 | |||||
| chr5:71463870
|
A | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0088a0001c0001t0002g0089others(2): Show | 6 | HG02155.hp2 NA18989.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.600-188A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463870 | ||||||
| chr5:71463873
|
T | C | 1 | a0003c0003t0001g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.600-185T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463873 | ||||||
| chr5:71463930
|
C | T | 2 | a0006c0007t0002g0006a0006c0028t0021g0008 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.600-128C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463930 | ||||||
| chr5:71463937
|
G | A | 1 | a0008c0009t0002g0110 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.600-121G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 3/38 | chr5 | 71463937 | ||||||
| chr5:71464164
|
A | C | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.659+47A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464164 | ||||||
| chr5:71464256
|
G | A | 1 | a0002c0002t0001g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.659+139G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464256 | ||||||
| chr5:71464411
|
C | T | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.659+294C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464411 | ||||||
| chr5:71464595
|
G | A | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.659+478G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464595 | ||||||
| chr5:71464640
|
C | T | 1 | a0003c0003t0001g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.659+523C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464640 | ||||||
| chr5:71464715
|
G | GT | 35 | a0001c0001t0002g0015a0001c0001t0002g0074a0001c0001t0002g0075others(32): Show | 35 | HG00423.hp2 HG00597.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.659+620dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr5 | 71464715 | |||||
| chr5:71464715
|
G | GTT | 10 | a0002c0002t0001g0142a0004c0004t0004g0318a0004c0004t0004g0320others(7): Show | 10 | HG01167.hp1 HG01257.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.659+619_659+620dup others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr5 | 71464715 | |||||
| chr5:71464715
|
G | GTTT | 86 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(83): Show | 87 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.659+618_659+620dup others(3): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr5 | 71464715 | |||||
| chr5:71464715
|
G | GTTTT | 15 | a0002c0002t0001g0208a0002c0002t0001g0210a0002c0002t0001g0211others(12): Show | 15 | HG00438.hp1 HG00735.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.659+617_659+620dup others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr5 | 71464715 | |||||
| chr5:71464952
|
C | T | 1 | a0010c0012t0003g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.659+835C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464952 | ||||||
| chr5:71464959
|
G | C | 1 | a0003c0003t0001g0292 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.659+842G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464959 | ||||||
| chr5:71464964
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.659+847G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71464964 | ||||||
| chr5:71465022
|
T | G | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.659+905T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465022 | ||||||
| chr5:71465095
|
T | G | 7 | a0006c0007t0002g0103a0006c0007t0002g0105a0006c0007t0002g0106others(4): Show | 7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.659+978T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465095 | ||||||
| chr5:71465131
|
A | G | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.660-965A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465131 | ||||||
| chr5:71465464
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | NA18945.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.660-632A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465464 | ||||||
| chr5:71465609
|
A | C | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.660-487A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465609 | ||||||
| chr5:71465612
|
G | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.660-484G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465612 | ||||||
| chr5:71465623
|
C | G | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.660-473C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465623 | ||||||
| chr5:71465665
|
G | A | 3 | a0005c0005t0001g0296a0005c0005t0001g0298a0005c0005t0017g0297 | 3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.660-431G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465665 | ||||||
| chr5:71465711
|
T | A | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.660-385T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465711 | ||||||
| chr5:71465813
|
G | A | 1 | a0031c0029t0004g0317 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.660-283G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465813 | ||||||
| chr5:71465887
|
A | G | 1 | a0002c0002t0001g0203 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.660-209A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 4/38 | chr5 | 71465887 | ||||||
| chr5:71466330
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.785+109C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466330 | ||||||
| chr5:71466364
|
A | G | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.785+143A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466364 | ||||||
| chr5:71466426
|
G | A | 6 | a0009c0008t0002g0007a0009c0008t0002g0090a0009c0008t0007g0095others(3): Show | 6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.785+205G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466426 | ||||||
| chr5:71466463
|
A | T | 1 | a0011c0011t0001g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.785+242A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466463 | ||||||
| chr5:71466620
|
A | G | 112 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(109): Show | 114 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.785+399A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466620 | ||||||
| chr5:71466749
|
GT | G | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.785+537delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr5 | 71466749 | |||||
| chr5:71466897
|
G | A | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.786-457G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466897 | ||||||
| chr5:71466954
|
A | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.786-400A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71466954 | ||||||
| chr5:71467062
|
C | G | 322 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(319): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.786-292C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467062 | ||||||
| chr5:71467075
|
C | G | 5 | a0002c0002t0001g0135a0002c0002t0001g0200a0002c0002t0001g0201others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.786-279C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467075 | ||||||
| chr5:71467084
|
T | C | 2 | a0021c0020t0023g0119a0022c0019t0024g0118 | 2 | HG00642.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.786-270T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467084 | ||||||
| chr5:71467108
|
G | A | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.786-246G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467108 | ||||||
| chr5:71467125
|
T | C | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.786-229T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467125 | ||||||
| chr5:71467232
|
G | A | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.786-122G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467232 | ||||||
| chr5:71467261
|
A | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.786-93A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467261 | ||||||
| chr5:71467283
|
T | C | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.786-71T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467283 | ||||||
| chr5:71467297
|
T | A | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.786-57T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 5/38 | chr5 | 71467297 | ||||||
| chr5:71467622
|
C | T | 1 | a0008c0009t0002g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.919+135C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71467622 | ||||||
| chr5:71467634
|
C | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.919+147C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71467634 | ||||||
| chr5:71467731
|
C | A | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+244C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71467731 | ||||||
| chr5:71468022
|
T | A | 1 | a0002c0002t0001g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.919+535T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468022 | ||||||
| chr5:71468135
|
C | T | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.919+648C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468135 | ||||||
| chr5:71468175
|
C | T | 1 | a0005c0005t0001g0299 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.919+688C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468175 | ||||||
| chr5:71468258
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.919+771G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468258 | ||||||
| chr5:71468453
|
A | T | 1 | a0037c0033t0003g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.919+966A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468453 | ||||||
| chr5:71468453
|
AT | A | 14 | a0001c0001t0002g0117a0002c0002t0001g0142a0003c0003t0001g0305others(11): Show | 15 | HG01257.hp2 HG01884.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.919+981delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr5 | 71468453 | |||||
| chr5:71468468
|
T | A | 6 | a0002c0002t0001g0222a0002c0002t0001g0224a0002c0002t0001g0225others(3): Show | 6 | HG00673.hp1 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+981T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468468 | ||||||
| chr5:71468607
|
C | CT | 217 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(214): Show | 220 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.919+1136dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr5 | 71468607 | |||||
| chr5:71468731
|
C | T | 12 | a0003c0003t0001g0232a0003c0003t0001g0274a0003c0003t0001g0275others(9): Show | 12 | HG02055.hp1 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+1244C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468731 | ||||||
| chr5:71468782
|
T | G | 1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919+1295T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468782 | ||||||
| chr5:71468826
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.919+1339C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468826 | ||||||
| chr5:71468906
|
C | T | 1 | a0003c0003t0001g0273 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.919+1419C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468906 | ||||||
| chr5:71468917
|
T | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.919+1430T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468917 | ||||||
| chr5:71468924
|
A | C | 27 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.919+1437A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468924 | ||||||
| chr5:71468983
|
T | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.920-1412T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71468983 | ||||||
| chr5:71469054
|
T | A | 104 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(101): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.920-1341T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469054 | ||||||
| chr5:71469322
|
A | G | 1 | a0001c0022t0002g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.920-1073A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469322 | ||||||
| chr5:71469366
|
T | C | 1 | a0004c0004t0010g0321 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.920-1029T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469366 | ||||||
| chr5:71469425
|
C | G | 3 | a0017c0017t0009g0115a0017c0017t0009g0116a0041c0047t0001g0228 | 3 | HG02622.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.920-970C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469425 | ||||||
| chr5:71469645
|
G | A | 5 | a0017c0017t0009g0115a0017c0017t0009g0116a0035c0032t0001g0114others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-750G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469645 | ||||||
| chr5:71469725
|
T | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.920-670T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469725 | ||||||
| chr5:71469762
|
C | T | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.920-633C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469762 | ||||||
| chr5:71469770
|
C | T | 1 | a0001c0022t0002g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.920-625C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469770 | ||||||
| chr5:71469813
|
C | T | 1 | a0002c0002t0001g0199 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.920-582C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469813 | ||||||
| chr5:71469842
|
C | CT | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.920-537dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr5 | 71469842 | |||||
| chr5:71469878
|
G | A | 1 | a0004c0004t0010g0321 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.920-517G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469878 | ||||||
| chr5:71469911
|
G | T | 10 | a0002c0002t0001g0142a0002c0002t0001g0195a0002c0002t0001g0196others(7): Show | 10 | HG01257.hp2 HG02071.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-484G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469911 | ||||||
| chr5:71469934
|
C | T | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-461C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469934 | ||||||
| chr5:71469945
|
G | A | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.920-450G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71469945 | ||||||
| chr5:71470088
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.920-307G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71470088 | ||||||
| chr5:71470130
|
C | G | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.920-265C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71470130 | ||||||
| chr5:71470293
|
C | A | 1 | a0005c0005t0001g0299 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.920-102C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 6/38 | chr5 | 71470293 | ||||||
| chr5:71470595
|
T | G | 2 | a0001c0001t0002g0074a0001c0001t0019g0016 | 2 | HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1014+106T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470595 | ||||||
| chr5:71470612
|
A | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1014+123A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470612 | ||||||
| chr5:71470655
|
C | T | 1 | a0006c0007t0002g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1014+166C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470655 | ||||||
| chr5:71470744
|
C | T | 6 | a0005c0005t0015g0310a0017c0017t0009g0115a0017c0017t0009g0116others(3): Show | 6 | HG00741.hp1 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+255C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470744 | ||||||
| chr5:71470833
|
C | T | 1 | a0003c0003t0001g0272 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1014+344C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470833 | ||||||
| chr5:71470891
|
C | CT | 22 | a0001c0026t0002g0012a0004c0004t0004g0311a0004c0004t0004g0312others(19): Show | 22 | HG01433.hp1 HG01884.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.1014+415dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71470891 | |||||
| chr5:71470892
|
T | G | 1 | a0001c0001t0002g0117 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1014+403T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470892 | ||||||
| chr5:71470913
|
A | T | 104 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(101): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1014+424A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71470913 | ||||||
| chr5:71471138
|
C | CT | 18 | a0001c0001t0002g0059a0001c0001t0002g0086a0001c0001t0002g0089others(15): Show | 18 | HG00642.hp2 HG00733.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1014+671dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71471138 | |||||
| chr5:71471138
|
C | CTT | 10 | a0004c0004t0004g0314a0004c0004t0004g0315a0004c0004t0004g0316others(7): Show | 10 | HG01433.hp1 HG02965.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014+670_1014+671d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71471138 | |||||
| chr5:71471138
|
CT | C | 10 | a0001c0001t0002g0125a0002c0002t0001g0145a0002c0002t0001g0302others(7): Show | 10 | HG00099.hp2 HG01070.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014+671delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71471138 | |||||
| chr5:71471150
|
T | G | 1 | a0013c0013t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1014+661T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471150 | ||||||
| chr5:71471173
|
C | T | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1014+684C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471173 | ||||||
| chr5:71471174
|
G | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+685G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471174 | ||||||
| chr5:71471287
|
C | T | 6 | a0005c0005t0015g0310a0017c0017t0009g0115a0017c0017t0009g0116others(3): Show | 6 | HG00741.hp1 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+798C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471287 | ||||||
| chr5:71471289
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+800C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471289 | ||||||
| chr5:71471329
|
A | T | 3 | a0005c0005t0001g0235a0005c0005t0001g0236a0005c0005t0001g0237 | 3 | HG01884.hp2 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1014+840A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471329 | ||||||
| chr5:71471423
|
C | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1014+934C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471423 | ||||||
| chr5:71471442
|
T | C | 257 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(254): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1014+953T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471442 | ||||||
| chr5:71471540
|
G | A | 10 | a0002c0002t0001g0142a0002c0002t0001g0195a0002c0002t0001g0196others(7): Show | 10 | HG01257.hp2 HG02071.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014+1051G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471540 | ||||||
| chr5:71471641
|
C | G | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1014+1152C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471641 | ||||||
| chr5:71471817
|
A | G | 6 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0057others(3): Show | 6 | HG01346.hp1 HG03239.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1014+1328A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71471817 | ||||||
| chr5:71472030
|
T | A | 1 | a0019c0050t0001g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1014+1541T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472030 | ||||||
| chr5:71472049
|
C | A | 1 | a0001c0001t0019g0016 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1014+1560C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472049 | ||||||
| chr5:71472317
|
C | T | 2 | a0005c0005t0015g0310a0041c0047t0001g0228 | 2 | HG00741.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1014+1828C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472317 | ||||||
| chr5:71472839
|
A | C | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1014+2350A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472839 | ||||||
| chr5:71472853
|
C | G | 1 | a0005c0005t0015g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1014+2364C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472853 | ||||||
| chr5:71472876
|
TTC | T | 94 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(91): Show | 96 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1014+2399_1014+240 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71472876 | |||||
| chr5:71472887
|
TC | T | 24 | a0001c0001t0002g0015a0001c0001t0002g0018a0001c0001t0002g0019others(21): Show | 24 | HG01358.hp2 HG02015.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1014+2399delC | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472887 | ||||||
| chr5:71472888
|
C | CT | 6 | a0002c0002t0001g0146a0002c0002t0001g0201a0002c0041t0001g0144others(3): Show | 6 | HG01169.hp1 HG02559.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+2422dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71472888 | |||||
| chr5:71472888
|
C | CTT | 91 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(88): Show | 92 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1014+2421_1014+242 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71472888 | |||||
| chr5:71472888
|
C | CTTT | 11 | a0002c0002t0001g0186a0002c0002t0001g0187a0002c0002t0001g0190others(8): Show | 11 | HG00423.hp1 HG01099.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+2420_1014+242 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71472888 | |||||
| chr5:71472995
|
A | G | 1 | a0003c0003t0001g0295 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1014+2506A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71472995 | ||||||
| chr5:71473044
|
G | A | 1 | a0010c0012t0003g0148 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1014+2555G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473044 | ||||||
| chr5:71473072
|
A | G | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1014+2583A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473072 | ||||||
| chr5:71473119
|
A | G | 118 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(115): Show | 120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1014+2630A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473119 | ||||||
| chr5:71473262
|
A | AT | 7 | a0003c0003t0001g0230a0003c0003t0001g0231a0003c0003t0001g0266others(4): Show | 7 | HG02056.hp1 HG04199.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.1014+2803dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | |||||
| chr5:71473262
|
AT | A | 7 | a0003c0003t0001g0240a0003c0003t0006g0241a0005c0005t0001g0296others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1014+2803delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | |||||
| chr5:71473262
|
ATTTT | A | 8 | a0002c0002t0001g0229a0002c0002t0001g0303a0002c0002t0001g0304others(5): Show | 8 | HG01884.hp1 HG01975.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1014+2800_1014+280 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | |||||
| chr5:71473262
|
ATTTTT | A | 100 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(97): Show | 101 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1014+2799_1014+280 others(9): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | |||||
| chr5:71473262
|
ATTTTTT | A | 9 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0086others(6): Show | 9 | HG01243.hp2 HG01257.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014+2798_1014+280 others(10): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | |||||
| chr5:71473262
|
ATTTTTTT | A | 125 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(122): Show | 127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1014+2797_1014+280 others(11): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71473262 | |||||
| chr5:71473316
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1014+2827C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473316 | ||||||
| chr5:71473826
|
G | A | 1 | a0002c0002t0001g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1014+3337G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473826 | ||||||
| chr5:71473834
|
C | A | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1014+3345C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473834 | ||||||
| chr5:71473851
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0002g0117 | 2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1014+3362C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473851 | ||||||
| chr5:71473990
|
G | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(140): Show | 145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1014+3501G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71473990 | ||||||
| chr5:71474048
|
C | T | 1 | a0003c0003t0001g0265 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1014+3559C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474048 | ||||||
| chr5:71474080
|
T | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+3591T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474080 | ||||||
| chr5:71474595
|
C | T | 1 | a0002c0002t0001g0214 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1014+4106C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474595 | ||||||
| chr5:71474677
|
G | A | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0011g0061 | 3 | NA18992.hp1 NA19054.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1014+4188G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474677 | ||||||
| chr5:71474707
|
T | TGTG | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014+4223_1014+422 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71474707 | |||||
| chr5:71474769
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1014+4280C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474769 | ||||||
| chr5:71474859
|
AT | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+4371delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474859 | ||||||
| chr5:71474860
|
T | A | 112 | a0001c0001t0002g0099a0002c0002t0001g0132a0002c0002t0001g0135others(109): Show | 113 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1014+4371T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474860 | ||||||
| chr5:71474893
|
C | G | 1 | a0003c0003t0001g0273 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1014+4404C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474893 | ||||||
| chr5:71474907
|
G | C | 1 | a0003c0003t0001g0273 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1014+4418G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71474907 | ||||||
| chr5:71475034
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1014+4545C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475034 | ||||||
| chr5:71475071
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+4582C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475071 | ||||||
| chr5:71475085
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1014+4596T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475085 | ||||||
| chr5:71475330
|
G | A | 1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1014+4841G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475330 | ||||||
| chr5:71475463
|
T | A | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014+4974T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475463 | ||||||
| chr5:71475492
|
A | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1014+5003A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475492 | ||||||
| chr5:71475519
|
A | T | 9 | a0002c0002t0001g0136a0002c0002t0001g0214a0002c0002t0001g0222others(6): Show | 9 | HG00673.hp1 NA18943.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014+5030A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475519 | ||||||
| chr5:71475866
|
A | G | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1014+5377A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475866 | ||||||
| chr5:71475964
|
A | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1014+5475A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71475964 | ||||||
| chr5:71476204
|
C | T | 2 | a0006c0007t0002g0006a0006c0028t0021g0008 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1014+5715C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476204 | ||||||
| chr5:71476386
|
A | G | 1 | a0004c0004t0004g0318 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1014+5897A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476386 | ||||||
| chr5:71476550
|
C | CT | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.1014+6070dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71476550 | |||||
| chr5:71476550
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1014+6061C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476550 | ||||||
| chr5:71476623
|
C | G | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014+6134C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476623 | ||||||
| chr5:71476698
|
C | G | 1 | a0024c0042t0001g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1014+6209C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476698 | ||||||
| chr5:71476698
|
C | T | 6 | a0005c0005t0015g0310a0017c0017t0009g0115a0017c0017t0009g0116others(3): Show | 6 | HG00741.hp1 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+6209C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476698 | ||||||
| chr5:71476729
|
A | G | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1014+6240A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476729 | ||||||
| chr5:71476764
|
C | T | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1014+6275C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476764 | ||||||
| chr5:71476814
|
C | T | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1014+6325C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476814 | ||||||
| chr5:71476841
|
C | G | 1 | a0001c0001t0002g0072 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1014+6352C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476841 | ||||||
| chr5:71476848
|
C | T | 2 | a0002c0002t0001g0214a0002c0002t0001g0229 | 2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1014+6359C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71476848 | ||||||
| chr5:71477003
|
C | A | 1 | a0001c0001t0002g0060 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1014+6514C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477003 | ||||||
| chr5:71477058
|
C | A | 1 | a0005c0005t0001g0298 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1014+6569C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477058 | ||||||
| chr5:71477280
|
C | A | 3 | a0002c0002t0001g0153a0002c0002t0001g0154a0026c0040t0001g0152 | 3 | HG02080.hp2 NA18939.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1015-6562C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477280 | ||||||
| chr5:71477361
|
T | C | 142 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(139): Show | 144 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1015-6481T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477361 | ||||||
| chr5:71477492
|
T | C | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1015-6350T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477492 | ||||||
| chr5:71477507
|
G | T | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1015-6335G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477507 | ||||||
| chr5:71477581
|
T | A | 1 | a0002c0002t0001g0155 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1015-6261T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477581 | ||||||
| chr5:71477617
|
A | ATGTTTTC others(4): Show |
1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1015-6224_1015-622 others(15): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71477617 | |||||
| chr5:71477617
|
A | ATTTTTTC others(4): Show |
131 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(128): Show | 133 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1015-6218_1015-620 others(15): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71477617 | |||||
| chr5:71477624
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0121a0039c0031t0016g0010 | 2 | HG00438.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1015-6208_1015-620 others(16): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71477624 | |||||
| chr5:71477810
|
G | T | 1 | a0016c0014t0001g0005 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1015-6032G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477810 | ||||||
| chr5:71477978
|
C | T | 13 | a0001c0001t0002g0029a0001c0001t0002g0048a0001c0001t0002g0049others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1015-5864C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477978 | ||||||
| chr5:71477989
|
G | A | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1015-5853G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477989 | ||||||
| chr5:71477999
|
C | T | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1015-5843C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71477999 | ||||||
| chr5:71478045
|
G | T | 1 | a0012c0010t0006g0242 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1015-5797G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478045 | ||||||
| chr5:71478177
|
G | C | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-5665G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478177 | ||||||
| chr5:71478198
|
G | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-5644G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478198 | ||||||
| chr5:71478262
|
A | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1015-5580A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478262 | ||||||
| chr5:71478347
|
A | G | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1015-5495A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478347 | ||||||
| chr5:71478461
|
C | G | 1 | a0003c0003t0001g0264 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1015-5381C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478461 | ||||||
| chr5:71478549
|
A | G | 1 | a0024c0042t0001g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1015-5293A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478549 | ||||||
| chr5:71478559
|
A | G | 1 | a0005c0005t0015g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1015-5283A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478559 | ||||||
| chr5:71478644
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-5198C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478644 | ||||||
| chr5:71478653
|
T | C | 1 | a0002c0002t0001g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1015-5189T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478653 | ||||||
| chr5:71478659
|
A | AT | 19 | a0001c0001t0002g0059a0001c0026t0002g0012a0002c0002t0001g0222others(16): Show | 19 | HG00673.hp1 HG01433.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.1015-5171dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71478659 | |||||
| chr5:71478840
|
G | A | 294 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(291): Show | 297 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1015-5002G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478840 | ||||||
| chr5:71478973
|
T | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-4869T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71478973 | ||||||
| chr5:71479073
|
C | T | 1 | a0013c0013t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1015-4769C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479073 | ||||||
| chr5:71479111
|
C | T | 2 | a0011c0011t0001g0184a0011c0011t0001g0185 | 2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1015-4731C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479111 | ||||||
| chr5:71479586
|
G | A | 5 | a0005c0005t0001g0234a0005c0005t0001g0235a0005c0005t0001g0236others(2): Show | 5 | HG01884.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1015-4256G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479586 | ||||||
| chr5:71479776
|
G | A | 1 | a0003c0003t0001g0243 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1015-4066G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479776 | ||||||
| chr5:71479811
|
A | G | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1015-4031A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479811 | ||||||
| chr5:71479844
|
C | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-3998C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479844 | ||||||
| chr5:71479895
|
T | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-3947T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479895 | ||||||
| chr5:71479931
|
TCC | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1015-3910_1015-390 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479931 | ||||||
| chr5:71479933
|
C | T | 1 | a0015c0016t0001g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1015-3909C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479933 | ||||||
| chr5:71479939
|
G | A | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1015-3903G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479939 | ||||||
| chr5:71479975
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-3867C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71479975 | ||||||
| chr5:71480030
|
C | T | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1015-3812C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480030 | ||||||
| chr5:71480148
|
G | C | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1015-3694G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480148 | ||||||
| chr5:71480193
|
C | G | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1015-3649C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480193 | ||||||
| chr5:71480204
|
G | T | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1015-3638G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480204 | ||||||
| chr5:71480249
|
T | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-3593T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480249 | ||||||
| chr5:71480255
|
C | T | 3 | a0002c0002t0001g0198a0035c0032t0001g0114a0038c0035t0001g0123 | 3 | HG01243.hp2 HG02257.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1015-3587C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480255 | ||||||
| chr5:71480257
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1015-3585C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480257 | ||||||
| chr5:71480277
|
A | AT | 22 | a0003c0003t0001g0255a0003c0003t0001g0262a0003c0003t0001g0264others(19): Show | 22 | HG00741.hp1 HG01192.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1015-3535dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | |||||
| chr5:71480277
|
AT | A | 66 | a0002c0002t0001g0135a0002c0002t0001g0146a0002c0002t0001g0153others(63): Show | 67 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1015-3535delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | |||||
| chr5:71480277
|
ATT | A | 46 | a0002c0002t0001g0132a0002c0002t0001g0142a0002c0002t0001g0150others(43): Show | 46 | HG00280.hp1 HG00673.hp1 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.1015-3536_1015-353 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | |||||
| chr5:71480277
|
ATTTTTTT others(5): Show |
A | 1 | a0006c0007t0002g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1015-3546_1015-353 others(16): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | |||||
| chr5:71480277
|
ATTTTTTT others(6): Show |
A | 15 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0049others(12): Show | 15 | HG01192.hp1 HG02109.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1015-3547_1015-353 others(17): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | |||||
| chr5:71480277
|
ATTTTTTT others(7): Show |
A | 108 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(105): Show | 110 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1015-3548_1015-353 others(18): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | |||||
| chr5:71480277
|
ATTTTTTT others(8): Show |
A | 1 | a0002c0002t0001g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1015-3549_1015-353 others(19): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480277 | |||||
| chr5:71480291
|
T | C | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1015-3551T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480291 | ||||||
| chr5:71480381
|
G | A | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1015-3461G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480381 | ||||||
| chr5:71480559
|
T | C | 2 | a0002c0002t0001g0224a0002c0002t0001g0225 | 2 | NA18943.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1015-3283T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480559 | ||||||
| chr5:71480570
|
AT | A | 241 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(238): Show | 244 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1015-3258delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71480570 | |||||
| chr5:71480756
|
G | A | 1 | a0007c0006t0002g0042 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1015-3086G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480756 | ||||||
| chr5:71480882
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1015-2960A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480882 | ||||||
| chr5:71480943
|
A | C | 1 | a0004c0004t0004g0313 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1015-2899A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71480943 | ||||||
| chr5:71481099
|
G | A | 1 | a0028c0043t0001g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1015-2743G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481099 | ||||||
| chr5:71481129
|
G | T | 2 | a0003c0003t0001g0290a0003c0003t0001g0291 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1015-2713G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481129 | ||||||
| chr5:71481130
|
C | T | 1 | a0001c0001t0020g0052 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1015-2712C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481130 | ||||||
| chr5:71481131
|
G | A | 1 | a0002c0002t0001g0289 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1015-2711G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481131 | ||||||
| chr5:71481246
|
C | CT | 13 | a0002c0002t0001g0156a0004c0004t0004g0311a0004c0004t0004g0312others(10): Show | 13 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1015-2585dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71481246 | |||||
| chr5:71481391
|
G | GA | 94 | a0002c0002t0001g0135a0002c0002t0001g0136a0002c0002t0001g0140others(91): Show | 95 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1015-2427dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71481391 | |||||
| chr5:71481391
|
G | GAA | 22 | a0002c0002t0001g0132a0002c0002t0001g0170a0002c0002t0001g0180others(19): Show | 22 | HG00673.hp1 HG01261.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1015-2428_1015-242 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71481391 | |||||
| chr5:71481391
|
GA | G | 114 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(111): Show | 116 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1015-2427delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr5 | 71481391 | |||||
| chr5:71481425
|
G | A | 1 | a0003c0003t0001g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1015-2417G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481425 | ||||||
| chr5:71481434
|
C | T | 120 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1015-2408C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481434 | ||||||
| chr5:71481883
|
A | G | 1 | a0003c0003t0001g0238 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1015-1959A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481883 | ||||||
| chr5:71481984
|
T | C | 1 | a0028c0043t0001g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1015-1858T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71481984 | ||||||
| chr5:71482060
|
A | G | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1015-1782A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482060 | ||||||
| chr5:71482187
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1015-1655C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482187 | ||||||
| chr5:71482318
|
G | C | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1015-1524G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482318 | ||||||
| chr5:71482329
|
G | C | 1 | a0003c0003t0018g0307 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1015-1513G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482329 | ||||||
| chr5:71482495
|
G | A | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1015-1347G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482495 | ||||||
| chr5:71482633
|
A | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1015-1209A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482633 | ||||||
| chr5:71482658
|
T | C | 1 | a0002c0002t0001g0181 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1015-1184T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482658 | ||||||
| chr5:71482777
|
G | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1015-1065G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71482777 | ||||||
| chr5:71483210
|
T | C | 123 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1015-632T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71483210 | ||||||
| chr5:71483784
|
A | T | 2 | a0020c0018t0001g0191a0025c0038t0001g0141 | 2 | HG01978.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1015-58A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 7/38 | chr5 | 71483784 | ||||||
| chr5:71483920
|
A | G | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1069+24A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71483920 | ||||||
| chr5:71484038
|
T | G | 2 | a0004c0004t0010g0321a0004c0004t0010g0322 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1069+142T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484038 | ||||||
| chr5:71484393
|
C | G | 257 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(254): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1069+497C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484393 | ||||||
| chr5:71484428
|
A | G | 104 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(101): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1069+532A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484428 | ||||||
| chr5:71484572
|
A | G | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1069+676A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484572 | ||||||
| chr5:71484592
|
A | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1069+696A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484592 | ||||||
| chr5:71484639
|
A | G | 3 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0273 | 3 | NA18966.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1069+743A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484639 | ||||||
| chr5:71484762
|
C | T | 288 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(285): Show | 291 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1069+866C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484762 | ||||||
| chr5:71484803
|
C | T | 120 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1069+907C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484803 | ||||||
| chr5:71484824
|
A | G | 5 | a0003c0003t0006g0241a0012c0010t0006g0242a0012c0010t0006g0250others(2): Show | 5 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069+928A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484824 | ||||||
| chr5:71484946
|
C | G | 1 | a0005c0005t0001g0298 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1069+1050C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71484946 | ||||||
| chr5:71485247
|
C | T | 6 | a0002c0002t0001g0196a0002c0002t0001g0218a0002c0002t0001g0219others(3): Show | 6 | HG02071.hp1 HG02074.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.1070-1237C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485247 | ||||||
| chr5:71485327
|
A | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1070-1157A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485327 | ||||||
| chr5:71485337
|
T | A | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1070-1147T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485337 | ||||||
| chr5:71485591
|
T | C | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1070-893T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485591 | ||||||
| chr5:71485642
|
C | T | 1 | a0001c0022t0002g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1070-842C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485642 | ||||||
| chr5:71485824
|
G | A | 10 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(7): Show | 10 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.1070-660G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485824 | ||||||
| chr5:71485853
|
A | G | 8 | a0003c0003t0001g0230a0003c0003t0001g0243a0003c0003t0001g0249others(5): Show | 8 | HG02056.hp1 HG02080.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.1070-631A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485853 | ||||||
| chr5:71485927
|
T | C | 246 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(243): Show | 249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1070-557T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71485927 | ||||||
| chr5:71486385
|
TAAAC | T | 8 | a0005c0005t0001g0234a0005c0005t0001g0235a0005c0005t0001g0236others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070-94_1070-91del others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr5 | 71486385 | |||||
| chr5:71486453
|
C | G | 1 | a0002c0002t0001g0151 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1070-31C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 8/38 | chr5 | 71486453 | ||||||
| chr5:71486813
|
A | C | 1 | a0017c0017t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1213+186A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71486813 | ||||||
| chr5:71486851
|
C | G | 1 | a0001c0001t0002g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1213+224C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71486851 | ||||||
| chr5:71486878
|
C | G | 1 | a0015c0016t0001g0193 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1213+251C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71486878 | ||||||
| chr5:71487279
|
T | C | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1213+652T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487279 | ||||||
| chr5:71487327
|
C | T | 3 | a0004c0004t0004g0315a0006c0007t0002g0006a0006c0028t0021g0008 | 3 | HG02895.hp2 HG02965.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1213+700C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487327 | ||||||
| chr5:71487599
|
C | T | 2 | a0006c0007t0002g0006a0006c0028t0021g0008 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1213+972C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487599 | ||||||
| chr5:71487673
|
C | G | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1213+1046C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487673 | ||||||
| chr5:71487755
|
C | T | 1 | a0003c0003t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1213+1128C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487755 | ||||||
| chr5:71487772
|
A | G | 1 | a0002c0002t0001g0304 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1213+1145A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487772 | ||||||
| chr5:71487787
|
A | G | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1213+1160A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71487787 | ||||||
| chr5:71488370
|
G | T | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1214-1034G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488370 | ||||||
| chr5:71488431
|
C | CT | 13 | a0003c0003t0001g0292a0004c0004t0004g0311a0004c0004t0004g0312others(10): Show | 13 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1214-959dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr5 | 71488431 | |||||
| chr5:71488663
|
A | G | 1 | a0003c0003t0001g0254 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1214-741A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488663 | ||||||
| chr5:71488799
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1214-605C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488799 | ||||||
| chr5:71488889
|
G | A | 1 | a0003c0003t0001g0284 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1214-515G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488889 | ||||||
| chr5:71488983
|
C | A | 1 | a0001c0001t0002g0094 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1214-421C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488983 | ||||||
| chr5:71488992
|
G | A | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1214-412G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71488992 | ||||||
| chr5:71489148
|
T | C | 1 | a0002c0002t0001g0145 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1214-256T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489148 | ||||||
| chr5:71489202
|
A | G | 2 | a0020c0018t0001g0191a0025c0038t0001g0141 | 2 | HG01978.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1214-202A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489202 | ||||||
| chr5:71489232
|
C | T | 1 | a0003c0003t0001g0282 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1214-172C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489232 | ||||||
| chr5:71489233
|
G | A | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1214-171G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489233 | ||||||
| chr5:71489381
|
A | G | 1 | a0006c0028t0021g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1214-23A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 9/38 | chr5 | 71489381 | ||||||
| chr5:71489824
|
G | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1492+142G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71489824 | ||||||
| chr5:71489996
|
A | G | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1492+314A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71489996 | ||||||
| chr5:71490186
|
C | T | 7 | a0006c0007t0002g0103a0006c0007t0002g0105a0006c0007t0002g0106others(4): Show | 7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1492+504C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490186 | ||||||
| chr5:71490204
|
A | G | 1 | a0001c0001t0020g0052 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1492+522A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490204 | ||||||
| chr5:71490336
|
T | C | 1 | a0002c0002t0012g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1493-648T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490336 | ||||||
| chr5:71490386
|
A | G | 6 | a0009c0008t0002g0007a0009c0008t0002g0090a0009c0008t0007g0095others(3): Show | 6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1493-598A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490386 | ||||||
| chr5:71490619
|
G | T | 1 | a0002c0002t0003g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1493-365G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490619 | ||||||
| chr5:71490888
|
T | G | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1493-96T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490888 | ||||||
| chr5:71490899
|
G | GAC | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1493-84_1493-83ins others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr5 | 71490899 | |||||
| chr5:71490921
|
T | C | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1493-63T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 10/38 | chr5 | 71490921 | ||||||
| chr5:71491164
|
A | C | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1640+33A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491164 | ||||||
| chr5:71491196
|
TC | T | 5 | a0017c0017t0009g0115a0017c0017t0009g0116a0035c0032t0001g0114others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640+66delC | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491196 | ||||||
| chr5:71491369
|
T | C | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1640+238T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491369 | ||||||
| chr5:71491478
|
CTTGCTGT others(67): Show |
C | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1640+349_1640+422d others(76): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr5 | 71491478 | |||||
| chr5:71491715
|
G | T | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1640+584G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491715 | ||||||
| chr5:71491759
|
G | C | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1640+628G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491759 | ||||||
| chr5:71491873
|
A | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1640+742A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71491873 | ||||||
| chr5:71492222
|
G | T | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1640+1091G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492222 | ||||||
| chr5:71492263
|
G | A | 1 | a0003c0003t0001g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1640+1132G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492263 | ||||||
| chr5:71492274
|
A | G | 3 | a0004c0004t0004g0311a0004c0004t0004g0319a0004c0004t0004g0320 | 3 | HG02027.hp1 NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1640+1143A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492274 | ||||||
| chr5:71492341
|
A | G | 1 | a0013c0013t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1640+1210A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492341 | ||||||
| chr5:71492350
|
A | G | 1 | a0003c0003t0001g0267 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1640+1219A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492350 | ||||||
| chr5:71492369
|
G | T | 1 | a0005c0005t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1640+1238G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492369 | ||||||
| chr5:71492426
|
T | C | 3 | a0016c0014t0001g0004a0016c0014t0001g0005a0022c0019t0024g0118 | 3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1640+1295T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492426 | ||||||
| chr5:71492627
|
G | C | 1 | a0007c0006t0002g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1640+1496G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492627 | ||||||
| chr5:71492784
|
T | A | 1 | a0002c0002t0001g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1640+1653T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492784 | ||||||
| chr5:71492802
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1640+1671G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492802 | ||||||
| chr5:71492867
|
A | G | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1640+1736A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492867 | ||||||
| chr5:71492920
|
G | C | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1640+1789G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71492920 | ||||||
| chr5:71493178
|
G | C | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1640+2047G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493178 | ||||||
| chr5:71493525
|
C | T | 1 | a0003c0003t0001g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1641-1725C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493525 | ||||||
| chr5:71493552
|
A | C | 3 | a0016c0014t0001g0004a0016c0014t0001g0005a0022c0019t0024g0118 | 3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1641-1698A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493552 | ||||||
| chr5:71493575
|
G | A | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1641-1675G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493575 | ||||||
| chr5:71493633
|
C | A | 1 | a0005c0005t0017g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1641-1617C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493633 | ||||||
| chr5:71493766
|
G | C | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1641-1484G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493766 | ||||||
| chr5:71493852
|
G | C | 1 | a0011c0011t0001g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1641-1398G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493852 | ||||||
| chr5:71493897
|
T | A | 2 | a0013c0013t0001g0003a0013c0013t0001g0133 | 3 | NA18989.hp2 NA19004.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1641-1353T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493897 | ||||||
| chr5:71493923
|
A | C | 1 | a0010c0012t0003g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1641-1327A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71493923 | ||||||
| chr5:71494024
|
A | T | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1641-1226A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494024 | ||||||
| chr5:71494039
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1641-1211C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494039 | ||||||
| chr5:71494173
|
A | G | 1 | a0005c0005t0015g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1641-1077A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494173 | ||||||
| chr5:71494349
|
A | C | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1641-901A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494349 | ||||||
| chr5:71494360
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1641-890G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494360 | ||||||
| chr5:71494363
|
G | A | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1641-887G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494363 | ||||||
| chr5:71494443
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1641-807C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494443 | ||||||
| chr5:71494471
|
G | C | 2 | a0003c0003t0001g0293a0003c0003t0001g0294 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1641-779G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494471 | ||||||
| chr5:71494538
|
A | G | 2 | a0003c0003t0001g0249a0003c0003t0001g0270 | 2 | NA18959.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1641-712A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494538 | ||||||
| chr5:71494549
|
A | G | 1 | a0002c0002t0003g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1641-701A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494549 | ||||||
| chr5:71494707
|
T | C | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1641-543T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494707 | ||||||
| chr5:71494794
|
G | A | 1 | a0002c0002t0001g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1641-456G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494794 | ||||||
| chr5:71494871
|
G | A | 1 | a0005c0005t0015g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1641-379G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494871 | ||||||
| chr5:71494901
|
G | T | 1 | a0001c0001t0002g0063 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1641-349G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71494901 | ||||||
| chr5:71495032
|
G | A | 5 | a0016c0014t0001g0004a0016c0014t0001g0005a0017c0017t0009g0115others(2): Show | 5 | HG00733.hp1 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1641-218G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71495032 | ||||||
| chr5:71495159
|
G | T | 1 | a0002c0002t0001g0210 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1641-91G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71495159 | ||||||
| chr5:71495183
|
T | A | 103 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(100): Show | 104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1641-67T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | chr5 | 71495183 | ||||||
| chr5:71495239
|
C | CT | 5 | a0016c0014t0001g0004a0016c0014t0001g0005a0017c0017t0009g0115others(2): Show | 5 | HG00733.hp1 HG02622.hp1 HG03130.hp2 others(2): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1641-3dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 11/38 | INFO_REALIGN_3_PRIME | chr5 | 71495239 | |||||
| chr5:71495438
|
A | G | 2 | a0005c0005t0001g0234a0005c0005t0001g0299 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1799+30A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495438 | ||||||
| chr5:71495518
|
T | C | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1799+110T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495518 | ||||||
| chr5:71495558
|
A | G | 2 | a0002c0002t0001g0302a0002c0002t0001g0304 | 2 | HG02071.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1799+150A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495558 | ||||||
| chr5:71495800
|
C | A | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1799+392C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495800 | ||||||
| chr5:71495937
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1799+529C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71495937 | ||||||
| chr5:71496128
|
G | C | 1 | a0001c0022t0002g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1799+720G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496128 | ||||||
| chr5:71496181
|
G | A | 1 | a0002c0039t0001g0207 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1799+773G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496181 | ||||||
| chr5:71496241
|
C | CA | 7 | a0001c0001t0002g0057a0001c0001t0002g0117a0001c0001t0002g0130others(4): Show | 7 | HG01943.hp1 HG01943.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1799+849dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496241 | |||||
| chr5:71496241
|
C | CAA | 135 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(132): Show | 137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1799+848_1799+849d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496241 | |||||
| chr5:71496308
|
A | G | 1 | a0033c0027t0002g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1799+900A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496308 | ||||||
| chr5:71496372
|
C | T | 5 | a0003c0003t0001g0240a0003c0003t0001g0255a0003c0003t0001g0286others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1800-898C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496372 | ||||||
| chr5:71496438
|
A | AT | 108 | a0001c0026t0002g0012a0002c0002t0001g0135a0002c0002t0001g0136others(105): Show | 109 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1800-815dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | |||||
| chr5:71496438
|
A | ATT | 20 | a0002c0002t0001g0132a0002c0002t0001g0168a0002c0002t0001g0225others(17): Show | 20 | HG01433.hp1 HG01884.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.1800-816_1800-815d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | |||||
| chr5:71496438
|
A | ATTT | 6 | a0001c0001t0002g0001a0001c0001t0002g0032a0001c0001t0002g0041others(3): Show | 7 | HG00609.hp2 HG03710.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1800-817_1800-815d others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | |||||
| chr5:71496438
|
A | ATTTT | 100 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0018others(97): Show | 101 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1800-818_1800-815d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | |||||
| chr5:71496438
|
A | ATTTTT | 12 | a0001c0001t0002g0014a0001c0001t0002g0048a0001c0001t0002g0080others(9): Show | 12 | HG00621.hp2 HG01109.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1800-819_1800-815d others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr5 | 71496438 | |||||
| chr5:71496645
|
C | G | 1 | a0002c0002t0003g0179 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1800-625C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496645 | ||||||
| chr5:71496714
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1800-556C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496714 | ||||||
| chr5:71496756
|
T | C | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1800-514T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496756 | ||||||
| chr5:71496859
|
A | G | 7 | a0016c0014t0001g0004a0016c0014t0001g0005a0017c0017t0009g0115others(4): Show | 7 | HG00733.hp1 HG01243.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1800-411A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496859 | ||||||
| chr5:71496875
|
G | C | 1 | a0001c0001t0002g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1800-395G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71496875 | ||||||
| chr5:71497083
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1800-187T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71497083 | ||||||
| chr5:71497115
|
A | G | 1 | a0033c0027t0002g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1800-155A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71497115 | ||||||
| chr5:71497190
|
A | G | 1 | a0017c0017t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1800-80A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71497190 | ||||||
| chr5:71497197
|
A | C | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1800-73A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 12/38 | chr5 | 71497197 | ||||||
| chr5:71497486
|
G | A | 4 | a0003c0003t0001g0256a0003c0003t0001g0257a0003c0003t0001g0258others(1): Show | 4 | HG00099.hp1 HG01255.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+60G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71497486 | ||||||
| chr5:71497486
|
G | T | 2 | a0002c0002t0001g0146a0002c0002t0001g0181 | 2 | NA18942.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1956+60G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71497486 | ||||||
| chr5:71497744
|
A | G | 104 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(101): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1956+318A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71497744 | ||||||
| chr5:71498154
|
G | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1956+728G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498154 | ||||||
| chr5:71498179
|
T | C | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1956+753T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498179 | ||||||
| chr5:71498302
|
A | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+876A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498302 | ||||||
| chr5:71498335
|
A | T | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1956+909A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498335 | ||||||
| chr5:71498367
|
G | A | 1 | a0003c0003t0001g0274 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1956+941G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498367 | ||||||
| chr5:71498390
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1956+964C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498390 | ||||||
| chr5:71498430
|
C | CT | 12 | a0003c0003t0001g0243a0004c0004t0004g0311a0004c0004t0004g0312others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1956+1015dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71498430 | |||||
| chr5:71498478
|
C | T | 1 | a0002c0002t0003g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1956+1052C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498478 | ||||||
| chr5:71498626
|
G | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+1200G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498626 | ||||||
| chr5:71498644
|
G | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+1218G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498644 | ||||||
| chr5:71498725
|
C | CT | 10 | a0003c0003t0001g0270a0006c0007t0002g0103a0006c0007t0002g0105others(7): Show | 10 | HG02258.hp1 HG02896.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1956+1315dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71498725 | |||||
| chr5:71498755
|
G | T | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1956+1329G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498755 | ||||||
| chr5:71498880
|
C | T | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1956+1454C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71498880 | ||||||
| chr5:71499078
|
A | G | 2 | a0002c0002t0001g0167a0002c0002t0001g0170 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1956+1652A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499078 | ||||||
| chr5:71499138
|
C | T | 7 | a0006c0007t0002g0103a0006c0007t0002g0105a0006c0007t0002g0106others(4): Show | 7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1956+1712C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499138 | ||||||
| chr5:71499141
|
C | T | 2 | a0002c0002t0001g0186a0002c0002t0001g0210 | 2 | HG01261.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1956+1715C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499141 | ||||||
| chr5:71499244
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+1818C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499244 | ||||||
| chr5:71499636
|
A | T | 8 | a0005c0005t0001g0234a0005c0005t0001g0235a0005c0005t0001g0236others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1957-1926A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499636 | ||||||
| chr5:71499653
|
C | T | 3 | a0005c0005t0001g0296a0005c0005t0001g0298a0005c0005t0017g0297 | 3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1957-1909C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499653 | ||||||
| chr5:71499669
|
T | C | 1 | a0004c0004t0004g0314 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1957-1893T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499669 | ||||||
| chr5:71499868
|
G | A | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1957-1694G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499868 | ||||||
| chr5:71499978
|
T | C | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1957-1584T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71499978 | ||||||
| chr5:71500051
|
TTC | T | 2 | a0013c0013t0001g0003a0013c0013t0001g0133 | 3 | NA18989.hp2 NA19004.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1957-1509_1957-150 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500051 | |||||
| chr5:71500288
|
T | C | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1957-1274T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71500288 | ||||||
| chr5:71500316
|
C | CT | 16 | a0003c0003t0001g0270a0003c0003t0001g0305a0003c0003t0018g0307others(13): Show | 16 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1957-1220dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | |||||
| chr5:71500316
|
CT | C | 27 | a0001c0001t0002g0089a0001c0001t0002g0094a0001c0026t0002g0012others(24): Show | 27 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1957-1220delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | |||||
| chr5:71500316
|
CTT | C | 110 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(107): Show | 112 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1957-1221_1957-122 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | |||||
| chr5:71500316
|
CTTT | C | 7 | a0001c0001t0002g0034a0001c0001t0002g0076a0001c0001t0002g0077others(4): Show | 7 | HG01070.hp1 HG01943.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1957-1222_1957-122 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | |||||
| chr5:71500316
|
CTTTTTTT others(2): Show |
C | 96 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(93): Show | 97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1957-1228_1957-122 others(13): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | |||||
| chr5:71500316
|
CTTTTTTT others(3): Show |
C | 4 | a0002c0002t0001g0201a0002c0002t0001g0214a0002c0002t0003g0206others(1): Show | 4 | HG01169.hp1 NA18985.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-1229_1957-122 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | |||||
| chr5:71500316
|
CTTTTTTT others(6): Show |
C | 2 | a0006c0007t0002g0006a0006c0028t0021g0008 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1957-1232_1957-122 others(17): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71500316 | |||||
| chr5:71500428
|
G | A | 2 | a0004c0004t0004g0312a0004c0004t0004g0316 | 2 | HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1957-1134G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71500428 | ||||||
| chr5:71500475
|
G | A | 13 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0067others(10): Show | 13 | HG00438.hp2 HG01943.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.1957-1087G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71500475 | ||||||
| chr5:71500872
|
G | C | 1 | a0001c0001t0002g0035 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1957-690G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71500872 | ||||||
| chr5:71501096
|
CA | C | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(133): Show | 138 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1957-450delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr5 | 71501096 | |||||
| chr5:71501270
|
C | T | 1 | a0003c0003t0001g0248 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1957-292C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71501270 | ||||||
| chr5:71501280
|
A | T | 1 | a0001c0001t0002g0101 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1957-282A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71501280 | ||||||
| chr5:71501429
|
C | T | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1957-133C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 13/38 | chr5 | 71501429 | ||||||
| chr5:71501672
|
G | C | 1 | a0002c0002t0001g0203 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2048+19G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71501672 | ||||||
| chr5:71501673
|
T | TA | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(100): Show | 105 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.2048+40dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71501673 | |||||
| chr5:71501673
|
T | TAA | 17 | a0001c0001t0002g0059a0001c0001t0002g0065a0001c0001t0002g0083others(14): Show | 17 | HG00423.hp2 HG01433.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2048+39_2048+40dup others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71501673 | |||||
| chr5:71501673
|
TA | T | 103 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(100): Show | 104 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.2048+40delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71501673 | |||||
| chr5:71501813
|
ACTCT | A | 3 | a0003c0003t0001g0243a0003c0003t0001g0249a0003c0003t0001g0270 | 3 | NA18959.hp1 NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2048+165_2048+168d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71501813 | |||||
| chr5:71501872
|
A | G | 2 | a0002c0002t0005g0178a0002c0002t0005g0189 | 2 | NA18963.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2048+219A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71501872 | ||||||
| chr5:71501875
|
T | A | 1 | a0002c0002t0001g0229 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2048+222T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71501875 | ||||||
| chr5:71502057
|
T | G | 1 | a0001c0001t0002g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2048+404T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502057 | ||||||
| chr5:71502189
|
CT | C | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2049-395delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr5 | 71502189 | |||||
| chr5:71502264
|
T | C | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2049-335T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502264 | ||||||
| chr5:71502314
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2049-285G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502314 | ||||||
| chr5:71502421
|
G | A | 101 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(98): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2049-178G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502421 | ||||||
| chr5:71502455
|
C | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2049-144C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 14/38 | chr5 | 71502455 | ||||||
| chr5:71502951
|
C | T | 1 | a0006c0024t0002g0104 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2241+160C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71502951 | ||||||
| chr5:71503019
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2241+228C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503019 | ||||||
| chr5:71503064
|
C | CA | 7 | a0001c0001t0002g0124a0001c0001t0002g0127a0002c0002t0003g0188others(4): Show | 7 | HG00423.hp1 HG01123.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2241+291dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr5 | 71503064 | |||||
| chr5:71503064
|
C | G | 9 | a0006c0007t0002g0006a0006c0007t0002g0103a0006c0007t0002g0105others(6): Show | 9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2241+273C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503064 | ||||||
| chr5:71503064
|
CA | C | 9 | a0001c0001t0002g0026a0002c0002t0001g0158a0003c0003t0001g0238others(6): Show | 9 | HG02523.hp2 HG02622.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2241+291delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr5 | 71503064 | |||||
| chr5:71503079
|
A | T | 7 | a0008c0009t0002g0028a0008c0009t0002g0053a0008c0009t0002g0110others(4): Show | 7 | HG02572.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2241+288A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503079 | ||||||
| chr5:71503503
|
A | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2241+712A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503503 | ||||||
| chr5:71503682
|
C | G | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2241+891C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71503682 | ||||||
| chr5:71504048
|
G | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2242-573G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504048 | ||||||
| chr5:71504064
|
A | AGATT | 9 | a0006c0007t0002g0006a0006c0007t0002g0103a0006c0007t0002g0105others(6): Show | 9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2242-554_2242-551d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr5 | 71504064 | |||||
| chr5:71504088
|
C | T | 1 | a0007c0006t0002g0044 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2242-533C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504088 | ||||||
| chr5:71504145
|
C | T | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2242-476C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504145 | ||||||
| chr5:71504165
|
C | T | 1 | a0003c0003t0001g0268 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2242-456C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504165 | ||||||
| chr5:71504190
|
A | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2242-431A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504190 | ||||||
| chr5:71504260
|
A | G | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2242-361A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504260 | ||||||
| chr5:71504272
|
C | CA | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2242-334dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | INFO_REALIGN_3_PRIME | chr5 | 71504272 | |||||
| chr5:71504396
|
T | G | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2242-225T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504396 | ||||||
| chr5:71504452
|
A | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.2242-169A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 15/38 | chr5 | 71504452 | ||||||
| chr5:71504868
|
G | A | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2372+117G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71504868 | ||||||
| chr5:71504998
|
A | G | 2 | a0007c0006t0002g0046a0007c0006t0002g0047 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2372+247A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71504998 | ||||||
| chr5:71505145
|
T | G | 6 | a0002c0002t0001g0222a0002c0002t0001g0224a0002c0002t0001g0225others(3): Show | 6 | HG00673.hp1 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.2372+394T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505145 | ||||||
| chr5:71505312
|
T | C | 3 | a0005c0005t0001g0296a0005c0005t0001g0298a0005c0005t0017g0297 | 3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2372+561T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505312 | ||||||
| chr5:71505497
|
T | A | 1 | a0032c0025t0002g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2372+746T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505497 | ||||||
| chr5:71505527
|
A | G | 247 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(244): Show | 250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.2372+776A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505527 | ||||||
| chr5:71505542
|
G | C | 4 | a0003c0003t0001g0244a0003c0003t0001g0247a0003c0003t0001g0252others(1): Show | 4 | HG00597.hp2 HG02155.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372+791G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505542 | ||||||
| chr5:71505584
|
C | T | 1 | a0003c0003t0001g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2372+833C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505584 | ||||||
| chr5:71505712
|
G | A | 118 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(115): Show | 120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2372+961G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505712 | ||||||
| chr5:71505761
|
T | G | 1 | a0003c0003t0001g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2372+1010T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71505761 | ||||||
| chr5:71506211
|
T | C | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2372+1460T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506211 | ||||||
| chr5:71506414
|
C | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2372+1663C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506414 | ||||||
| chr5:71506635
|
A | G | 2 | a0006c0007t0002g0006a0006c0028t0021g0008 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2372+1884A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506635 | ||||||
| chr5:71506758
|
T | TTA | 109 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(106): Show | 110 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2372+2029_2372+203 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | |||||
| chr5:71506758
|
T | TTATA | 9 | a0002c0002t0001g0159a0002c0002t0001g0172a0002c0002t0001g0214others(6): Show | 9 | HG00733.hp2 HG02027.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2372+2027_2372+203 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | |||||
| chr5:71506758
|
T | TTATATAT others(3): Show |
1 | a0016c0014t0001g0005 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2372+2021_2372+203 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | |||||
| chr5:71506758
|
T | TTATATAT others(13): Show |
1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2372+2011_2372+203 others(24): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | |||||
| chr5:71506758
|
T | TTATATAT others(19): Show |
1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2372+2030_2372+203 others(30): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | |||||
| chr5:71506758
|
T | TTATATAT others(25): Show |
1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2372+2030_2372+203 others(36): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | |||||
| chr5:71506758
|
TTA | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2372+2029_2372+203 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506758 | |||||
| chr5:71506786
|
A | AAC | 6 | a0001c0001t0002g0018a0003c0003t0001g0259a0003c0003t0001g0273others(3): Show | 6 | HG00642.hp2 HG01109.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.2372+2072_2372+207 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
A | AACAC | 17 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(14): Show | 17 | HG00673.hp2 HG00741.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2372+2070_2372+207 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
A | AACACAC | 8 | a0001c0001t0002g0050a0001c0001t0002g0087a0001c0001t0002g0094others(5): Show | 8 | HG01358.hp2 HG01433.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2372+2068_2372+207 others(10): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
A | AACACACA others(1): Show |
3 | a0004c0004t0004g0312a0005c0005t0015g0310a0009c0008t0002g0007 | 3 | HG00741.hp1 HG01167.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2372+2066_2372+207 others(12): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
A | AACACACA others(3): Show |
4 | a0004c0004t0004g0313a0004c0004t0004g0314a0004c0004t0010g0322others(1): Show | 4 | HG01943.hp1 HG02976.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2372+2064_2372+207 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
A | AACACACA others(5): Show |
1 | a0004c0004t0004g0318 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2372+2062_2372+207 others(16): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
A | AACACACA others(9): Show |
2 | a0004c0004t0004g0311a0004c0004t0010g0321 | 2 | HG02027.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2372+2058_2372+207 others(20): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
A | AACACACA others(11): Show |
1 | a0004c0004t0004g0319 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2372+2056_2372+207 others(22): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
A | AACACACA others(13): Show |
1 | a0004c0004t0004g0320 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2372+2054_2372+207 others(24): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
AAC | A | 85 | a0002c0002t0001g0135a0002c0002t0001g0140a0002c0002t0001g0142others(82): Show | 86 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.2372+2072_2372+207 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
AACACACA others(3): Show |
A | 22 | a0003c0003t0001g0230a0003c0003t0001g0238a0003c0003t0001g0243others(19): Show | 22 | HG00597.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2372+2064_2372+207 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506786
|
AACACACA others(5): Show |
A | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2372+2062_2372+207 others(16): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506786 | |||||
| chr5:71506819
|
A | C | 3 | a0002c0002t0001g0145a0002c0002t0001g0156a0002c0002t0001g0180 | 3 | HG01433.hp2 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2372+2068A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506819 | ||||||
| chr5:71506821
|
A | ACC | 4 | a0002c0002t0001g0150a0002c0002t0001g0153a0002c0002t0001g0154others(1): Show | 4 | HG02080.hp2 NA18939.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372+2071_2372+207 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506821 | |||||
| chr5:71506821
|
A | C | 83 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(80): Show | 84 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2372+2070A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506821 | ||||||
| chr5:71506823
|
A | ACACACAC others(3): Show |
4 | a0001c0001t0002g0085a0004c0004t0004g0315a0031c0029t0004g0317others(1): Show | 4 | HG03669.hp2 HG03710.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372+2073_2372+207 others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | |||||
| chr5:71506823
|
A | ACACACAC others(1): Show |
14 | a0001c0001t0002g0048a0001c0001t0002g0059a0001c0001t0002g0064others(11): Show | 14 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2372+2073_2372+207 others(12): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | |||||
| chr5:71506823
|
A | ACACACC | 44 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0015others(41): Show | 46 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2372+2073_2372+207 others(10): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | |||||
| chr5:71506823
|
A | ACACC | 16 | a0001c0001t0002g0023a0001c0001t0002g0062a0001c0001t0002g0063others(13): Show | 16 | HG01123.hp1 HG01496.hp1 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.2372+2073_2372+207 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | |||||
| chr5:71506823
|
A | ACC | 22 | a0001c0001t0002g0014a0001c0001t0002g0022a0001c0001t0002g0034others(19): Show | 22 | HG01070.hp1 HG01074.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2372+2074_2372+207 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71506823 | |||||
| chr5:71506823
|
A | C | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2372+2072A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506823 | ||||||
| chr5:71506935
|
C | T | 1 | a0002c0002t0001g0151 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2372+2184C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506935 | ||||||
| chr5:71506939
|
G | T | 1 | a0002c0002t0001g0151 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2372+2188G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506939 | ||||||
| chr5:71506957
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2372+2206A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71506957 | ||||||
| chr5:71507003
|
G | C | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2372+2252G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507003 | ||||||
| chr5:71507163
|
A | G | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2373-2302A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507163 | ||||||
| chr5:71507225
|
C | T | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2373-2240C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507225 | ||||||
| chr5:71507557
|
C | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2373-1908C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507557 | ||||||
| chr5:71507764
|
T | C | 1 | a0005c0005t0001g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2373-1701T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507764 | ||||||
| chr5:71507768
|
A | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.2373-1697A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507768 | ||||||
| chr5:71507795
|
G | A | 5 | a0003c0003t0001g0240a0003c0003t0001g0255a0003c0003t0001g0286others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2373-1670G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507795 | ||||||
| chr5:71507865
|
A | G | 1 | a0006c0007t0002g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2373-1600A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507865 | ||||||
| chr5:71507963
|
G | A | 2 | a0002c0002t0001g0151a0002c0002t0001g0159 | 2 | HG00280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2373-1502G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507963 | ||||||
| chr5:71507995
|
T | A | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2373-1470T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71507995 | ||||||
| chr5:71508050
|
C | T | 5 | a0010c0012t0003g0148a0010c0012t0003g0165a0010c0012t0003g0166others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2373-1415C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508050 | ||||||
| chr5:71508109
|
C | T | 2 | a0002c0002t0001g0132a0002c0002t0001g0301 | 2 | NA18993.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2373-1356C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508109 | ||||||
| chr5:71508112
|
G | A | 5 | a0005c0005t0001g0234a0005c0005t0001g0235a0005c0005t0001g0236others(2): Show | 5 | HG01884.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2373-1353G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508112 | ||||||
| chr5:71508471
|
A | AT | 244 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(241): Show | 247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2373-980dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71508471 | |||||
| chr5:71508611
|
T | C | 2 | a0036c0034t0003g0138a0037c0033t0003g0137 | 2 | HG02080.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2373-854T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508611 | ||||||
| chr5:71508769
|
A | C | 1 | a0002c0002t0001g0187 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2373-696A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508769 | ||||||
| chr5:71508794
|
G | A | 1 | a0006c0007t0002g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2373-671G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71508794 | ||||||
| chr5:71509048
|
G | A | 1 | a0001c0022t0002g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2373-417G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509048 | ||||||
| chr5:71509058
|
A | G | 1 | a0003c0003t0001g0272 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2373-407A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509058 | ||||||
| chr5:71509069
|
C | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.2373-396C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509069 | ||||||
| chr5:71509353
|
T | C | 117 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(114): Show | 119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.2373-112T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509353 | ||||||
| chr5:71509354
|
T | C | 1 | a0032c0025t0002g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2373-111T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509354 | ||||||
| chr5:71509442
|
T | C | 1 | a0002c0002t0001g0198 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2373-23T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509442 | ||||||
| chr5:71509445
|
GC | G | 118 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(115): Show | 120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2373-15delC | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71509445 | |||||
| chr5:71509450
|
C | T | 15 | a0001c0026t0002g0012a0004c0004t0004g0311a0004c0004t0004g0312others(12): Show | 15 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.2373-15C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | chr5 | 71509450 | ||||||
| chr5:71509450
|
CT | C | 71 | a0002c0002t0001g0135a0002c0002t0001g0140a0002c0002t0001g0142others(68): Show | 72 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(69): Show |
splice_region_variant&intron_variant | LOW | c.2373-5delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr5 | 71509450 | |||||
| chr5:71511189
|
CT | C | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.4059+44delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr5 | 71511189 | |||||
| chr5:71511246
|
C | T | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.4059+95C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511246 | ||||||
| chr5:71511661
|
A | G | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4059+510A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511661 | ||||||
| chr5:71511738
|
T | C | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.4060-503T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511738 | ||||||
| chr5:71511777
|
G | C | 1 | a0001c0001t0002g0100 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4060-464G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511777 | ||||||
| chr5:71511953
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4060-288A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511953 | ||||||
| chr5:71511982
|
A | G | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.4060-259A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71511982 | ||||||
| chr5:71512074
|
T | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4060-167T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71512074 | ||||||
| chr5:71512090
|
T | C | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4060-151T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71512090 | ||||||
| chr5:71512134
|
A | G | 1 | a0003c0003t0001g0272 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4060-107A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71512134 | ||||||
| chr5:71512164
|
G | A | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.4060-77G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 17/38 | chr5 | 71512164 | ||||||
| chr5:71512458
|
T | C | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4247+30T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512458 | ||||||
| chr5:71512467
|
A | G | 1 | a0028c0043t0001g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4247+39A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512467 | ||||||
| chr5:71512515
|
C | A | 3 | a0005c0005t0001g0296a0005c0005t0001g0298a0005c0005t0017g0297 | 3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.4247+87C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512515 | ||||||
| chr5:71512743
|
G | A | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.4247+315G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512743 | ||||||
| chr5:71512765
|
T | G | 5 | a0005c0005t0001g0233a0016c0014t0001g0004a0016c0014t0001g0005others(2): Show | 5 | HG00733.hp1 HG02258.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4247+337T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | chr5 | 71512765 | ||||||
| chr5:71513063
|
C | CA | 23 | a0002c0002t0001g0150a0002c0002t0001g0153a0002c0002t0001g0155others(20): Show | 23 | HG00621.hp1 HG00741.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.4248-97dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr5 | 71513063 | |||||
| chr5:71513063
|
CA | C | 93 | a0001c0001t0002g0036a0001c0001t0002g0059a0001c0001t0002g0083others(90): Show | 94 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.4248-97delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr5 | 71513063 | |||||
| chr5:71513063
|
CAA | C | 106 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(103): Show | 108 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.4248-98_4248-97del others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 18/38 | INFO_REALIGN_3_PRIME | chr5 | 71513063 | |||||
| chr5:71513426
|
G | A | 1 | a0033c0027t0002g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4470+19G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513426 | ||||||
| chr5:71513442
|
GT | G | 138 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(135): Show | 140 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.4470+50delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr5 | 71513442 | |||||
| chr5:71513513
|
G | C | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4470+106G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513513 | ||||||
| chr5:71513754
|
T | A | 2 | a0002c0002t0001g0214a0002c0002t0001g0229 | 2 | NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.4470+347T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513754 | ||||||
| chr5:71513755
|
C | G | 118 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(115): Show | 120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.4470+348C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513755 | ||||||
| chr5:71513775
|
A | G | 2 | a0002c0002t0001g0167a0002c0002t0001g0170 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4470+368A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513775 | ||||||
| chr5:71513813
|
A | G | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(140): Show | 145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.4470+406A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513813 | ||||||
| chr5:71513822
|
C | T | 1 | a0005c0005t0001g0299 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4470+415C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513822 | ||||||
| chr5:71513885
|
A | T | 1 | a0003c0003t0001g0253 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.4470+478A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513885 | ||||||
| chr5:71513984
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4470+577A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71513984 | ||||||
| chr5:71514011
|
C | T | 30 | a0003c0003t0001g0230a0003c0003t0001g0238a0003c0003t0001g0243others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4470+604C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514011 | ||||||
| chr5:71514116
|
C | A | 1 | a0005c0005t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4470+709C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514116 | ||||||
| chr5:71514208
|
A | G | 3 | a0001c0001t0002g0072a0001c0001t0002g0120a0001c0001t0002g0121 | 3 | HG00438.hp2 HG02040.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.4471-736A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514208 | ||||||
| chr5:71514209
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4471-735G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514209 | ||||||
| chr5:71514221
|
C | T | 255 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(252): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.4471-723C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514221 | ||||||
| chr5:71514567
|
T | C | 2 | a0005c0005t0001g0234a0005c0005t0001g0299 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4471-377T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514567 | ||||||
| chr5:71514597
|
G | A | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4471-347G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514597 | ||||||
| chr5:71514705
|
G | T | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4471-239G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514705 | ||||||
| chr5:71514763
|
T | G | 1 | a0005c0005t0015g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4471-181T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514763 | ||||||
| chr5:71514868
|
T | C | 2 | a0005c0005t0001g0234a0005c0005t0001g0299 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4471-76T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 19/38 | chr5 | 71514868 | ||||||
| chr5:71515275
|
T | C | 1 | a0003c0003t0001g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4649+153T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515275 | ||||||
| chr5:71515505
|
A | G | 1 | a0002c0002t0001g0197 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4649+383A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515505 | ||||||
| chr5:71515541
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0077 | 2 | NA19004.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.4649+419T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515541 | ||||||
| chr5:71515885
|
C | T | 1 | a0016c0014t0001g0005 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4650-176C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515885 | ||||||
| chr5:71515981
|
A | G | 3 | a0017c0017t0009g0115a0017c0017t0009g0116a0041c0047t0001g0228 | 3 | HG02622.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4650-80A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515981 | ||||||
| chr5:71515985
|
A | G | 3 | a0017c0017t0009g0115a0017c0017t0009g0116a0041c0047t0001g0228 | 3 | HG02622.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4650-76A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515985 | ||||||
| chr5:71515994
|
A | G | 111 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(108): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.4650-67A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 20/38 | chr5 | 71515994 | ||||||
| chr5:71516324
|
A | G | 3 | a0004c0004t0004g0311a0017c0017t0009g0115a0017c0017t0009g0116 | 3 | HG02027.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4860+53A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516324 | ||||||
| chr5:71516407
|
G | C | 1 | a0033c0027t0002g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4860+136G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516407 | ||||||
| chr5:71516418
|
C | T | 5 | a0001c0001t0002g0002a0001c0001t0002g0088a0001c0001t0002g0089others(2): Show | 6 | HG02155.hp2 NA18989.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.4860+147C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516418 | ||||||
| chr5:71516476
|
C | T | 4 | a0002c0002t0001g0172a0002c0002t0001g0186a0002c0002t0001g0190others(1): Show | 4 | HG00733.hp2 HG01099.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.4860+205C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516476 | ||||||
| chr5:71516485
|
A | G | 1 | a0036c0034t0003g0138 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4860+214A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516485 | ||||||
| chr5:71516517
|
G | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4860+246G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516517 | ||||||
| chr5:71516749
|
T | C | 6 | a0003c0003t0001g0231a0003c0003t0001g0240a0003c0003t0001g0255others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4860+478T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516749 | ||||||
| chr5:71516791
|
T | G | 1 | a0002c0002t0001g0160 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4860+520T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516791 | ||||||
| chr5:71516819
|
T | C | 1 | a0001c0001t0002g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4861-503T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71516819 | ||||||
| chr5:71517049
|
A | G | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4861-273A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71517049 | ||||||
| chr5:71517160
|
G | A | 2 | a0014c0015t0001g0221a0014c0015t0001g0223 | 2 | NA18974.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4861-162G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71517160 | ||||||
| chr5:71517268
|
A | T | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4861-54A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 21/38 | chr5 | 71517268 | ||||||
| chr5:71517846
|
G | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4991+394G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71517846 | ||||||
| chr5:71517954
|
T | A | 3 | a0005c0005t0001g0296a0005c0005t0001g0298a0005c0005t0017g0297 | 3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.4991+502T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71517954 | ||||||
| chr5:71518018
|
G | A | 1 | a0040c0045t0002g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4991+566G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518018 | ||||||
| chr5:71518062
|
G | A | 1 | a0006c0007t0002g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4991+610G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518062 | ||||||
| chr5:71518101
|
T | C | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.4991+649T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518101 | ||||||
| chr5:71518272
|
T | C | 105 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(102): Show | 106 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.4991+820T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518272 | ||||||
| chr5:71518342
|
G | C | 1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4991+890G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518342 | ||||||
| chr5:71518343
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4991+891G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518343 | ||||||
| chr5:71518355
|
T | A | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.4991+903T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518355 | ||||||
| chr5:71518373
|
T | C | 3 | a0005c0005t0001g0296a0005c0005t0001g0298a0005c0005t0017g0297 | 3 | HG02451.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.4991+921T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518373 | ||||||
| chr5:71518654
|
A | G | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4991+1202A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518654 | ||||||
| chr5:71518659
|
G | T | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.4991+1207G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518659 | ||||||
| chr5:71518835
|
C | CT | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.4991+1401dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71518835 | |||||
| chr5:71518835
|
CT | C | 99 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(96): Show | 100 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.4991+1401delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71518835 | |||||
| chr5:71518858
|
A | C | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4991+1406A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71518858 | ||||||
| chr5:71519111
|
C | T | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.4991+1659C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519111 | ||||||
| chr5:71519292
|
AC | A | 101 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(98): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.4991+1841delC | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519292 | ||||||
| chr5:71519377
|
T | A | 1 | a0001c0001t0002g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4991+1925T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519377 | ||||||
| chr5:71519622
|
A | G | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.4991+2170A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519622 | ||||||
| chr5:71519654
|
G | A | 1 | a0004c0004t0010g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4991+2202G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519654 | ||||||
| chr5:71519668
|
C | A | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4991+2216C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519668 | ||||||
| chr5:71519986
|
G | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4992-2303G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71519986 | ||||||
| chr5:71520114
|
G | C | 2 | a0014c0015t0001g0221a0014c0015t0001g0223 | 2 | NA18974.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4992-2175G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520114 | ||||||
| chr5:71520150
|
A | T | 2 | a0003c0003t0001g0240a0012c0010t0001g0239 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4992-2139A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520150 | ||||||
| chr5:71520157
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.4992-2132G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520157 | ||||||
| chr5:71520322
|
T | G | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4992-1967T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520322 | ||||||
| chr5:71520336
|
A | G | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.4992-1953A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520336 | ||||||
| chr5:71520379
|
C | T | 2 | a0005c0005t0001g0233a0029c0044t0005g0194 | 2 | NA18906.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.4992-1910C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520379 | ||||||
| chr5:71520674
|
T | TGCCAGGC others(264): Show |
2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4992-1600_4992-159 others(275): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71520674 | |||||
| chr5:71520690
|
A | G | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4992-1599A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71520690 | ||||||
| chr5:71521057
|
G | A | 1 | a0042c0052t0001g0226 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4992-1232G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521057 | ||||||
| chr5:71521083
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0002g0101a0001c0001t0002g0102 | 3 | HG00621.hp2 NA18949.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.4992-1206G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521083 | ||||||
| chr5:71521169
|
A | G | 1 | a0006c0007t0002g0006 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4992-1120A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521169 | ||||||
| chr5:71521187
|
C | CA | 18 | a0001c0001t0002g0035a0001c0001t0002g0072a0001c0001t0002g0120others(15): Show | 18 | HG00438.hp2 HG02040.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.4992-1087dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71521187 | |||||
| chr5:71521187
|
CA | C | 6 | a0017c0017t0009g0115a0017c0017t0009g0116a0021c0020t0023g0119others(3): Show | 6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4992-1087delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71521187 | |||||
| chr5:71521291
|
G | GT | 21 | a0001c0001t0002g0025a0001c0001t0002g0059a0001c0001t0002g0121others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.4992-981dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71521291 | |||||
| chr5:71521417
|
C | T | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4992-872C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521417 | ||||||
| chr5:71521592
|
T | C | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4992-697T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521592 | ||||||
| chr5:71521714
|
C | T | 1 | a0033c0027t0002g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4992-575C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521714 | ||||||
| chr5:71521804
|
G | A | 2 | a0004c0004t0004g0319a0004c0004t0004g0320 | 2 | NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.4992-485G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521804 | ||||||
| chr5:71521808
|
C | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.4992-481C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521808 | ||||||
| chr5:71521960
|
C | CT | 104 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(101): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.4992-318dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr5 | 71521960 | |||||
| chr5:71521982
|
G | C | 3 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0273 | 3 | NA18966.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.4992-307G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71521982 | ||||||
| chr5:71522073
|
A | G | 3 | a0016c0014t0001g0004a0016c0014t0001g0005a0022c0019t0024g0118 | 3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4992-216A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 22/38 | chr5 | 71522073 | ||||||
| chr5:71522502
|
C | CA | 132 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(129): Show | 134 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.5193+28dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr5 | 71522502 | |||||
| chr5:71522520
|
T | G | 1 | a0002c0002t0001g0225 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.5193+30T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | chr5 | 71522520 | ||||||
| chr5:71522540
|
G | T | 2 | a0002c0002t0001g0164a0002c0002t0001g0176 | 2 | HG02015.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.5193+50G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | chr5 | 71522540 | ||||||
| chr5:71522667
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5194-89A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | chr5 | 71522667 | ||||||
| chr5:71522705
|
C | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5194-51C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 23/38 | chr5 | 71522705 | ||||||
| chr5:71523050
|
A | G | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(140): Show | 145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.5387+101A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523050 | ||||||
| chr5:71523164
|
G | C | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5387+215G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523164 | ||||||
| chr5:71523353
|
C | T | 2 | a0003c0003t0001g0275a0003c0003t0001g0308 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.5387+404C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523353 | ||||||
| chr5:71523355
|
C | T | 2 | a0009c0008t0002g0007a0009c0008t0002g0090 | 2 | HG01167.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5387+406C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523355 | ||||||
| chr5:71523409
|
G | A | 17 | a0001c0001t0002g0014a0001c0001t0002g0022a0001c0001t0002g0030others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.5387+460G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523409 | ||||||
| chr5:71523468
|
C | T | 1 | a0034c0023t0002g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.5388-471C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 24/38 | chr5 | 71523468 | ||||||
| chr5:71524448
|
A | C | 1 | a0001c0001t0002g0059 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.5772+125A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524448 | ||||||
| chr5:71524540
|
C | CAAT | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+217_5772+218i others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524540 | ||||||
| chr5:71524566
|
C | T | 1 | a0003c0003t0001g0261 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5772+243C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524566 | ||||||
| chr5:71524592
|
A | AT | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+270dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71524592 | |||||
| chr5:71524633
|
ATTTTTTA others(5): Show |
A | 2 | a0006c0007t0002g0108a0006c0007t0002g0109 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.5772+317_5772+328d others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71524633 | |||||
| chr5:71524644
|
AT | A | 130 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(127): Show | 132 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.5772+330delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71524644 | |||||
| chr5:71524787
|
C | T | 31 | a0003c0003t0001g0230a0003c0003t0001g0238a0003c0003t0001g0243others(28): Show | 31 | HG00140.hp2 HG00597.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.5772+464C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524787 | ||||||
| chr5:71524825
|
T | TGGCGATG others(320): Show |
1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5772+515_5772+516i others(329): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71524825 | |||||
| chr5:71524986
|
G | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5772+663G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71524986 | ||||||
| chr5:71525007
|
A | C | 122 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(119): Show | 124 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.5772+684A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525007 | ||||||
| chr5:71525063
|
T | C | 1 | a0015c0016t0001g0193 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5772+740T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525063 | ||||||
| chr5:71525098
|
A | G | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.5772+775A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525098 | ||||||
| chr5:71525158
|
G | C | 8 | a0005c0005t0001g0234a0005c0005t0001g0235a0005c0005t0001g0236others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.5772+835G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525158 | ||||||
| chr5:71525189
|
A | C | 1 | a0001c0001t0002g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5772+866A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525189 | ||||||
| chr5:71525190
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5772+867C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525190 | ||||||
| chr5:71525223
|
G | A | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.5772+900G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525223 | ||||||
| chr5:71525245
|
T | C | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+922T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525245 | ||||||
| chr5:71525246
|
G | A | 111 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(108): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.5772+923G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525246 | ||||||
| chr5:71525268
|
C | CCCCCCCA others(41): Show |
1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5772+951_5772+952i others(50): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525268 | |||||
| chr5:71525269
|
CCCCCCCA others(170): Show |
C | 10 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(7): Show | 10 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.5772+985_5772+1161 others(3): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525269 | |||||
| chr5:71525286
|
C | T | 1 | a0003c0003t0001g0243 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5772+963C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525286 | ||||||
| chr5:71525303
|
C | T | 111 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(108): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.5772+980C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525303 | ||||||
| chr5:71525304
|
G | A | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5772+981G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525304 | ||||||
| chr5:71525329
|
G | A | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5772+1006G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525329 | ||||||
| chr5:71525362
|
C | G | 1 | a0002c0002t0001g0222 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5772+1039C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525362 | ||||||
| chr5:71525364
|
C | T | 1 | a0024c0042t0001g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5772+1041C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525364 | ||||||
| chr5:71525376
|
C | T | 1 | a0005c0005t0017g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5772+1053C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525376 | ||||||
| chr5:71525381
|
C | T | 1 | a0006c0007t0002g0006 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5772+1058C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525381 | ||||||
| chr5:71525414
|
G | A | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5772+1091G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525414 | ||||||
| chr5:71525417
|
C | T | 3 | a0011c0011t0001g0184a0011c0011t0001g0185a0022c0019t0024g0118 | 3 | HG01975.hp1 HG01981.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.5772+1094C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525417 | ||||||
| chr5:71525445
|
C | T | 282 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(279): Show | 285 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.5772+1122C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525445 | ||||||
| chr5:71525446
|
A | C | 283 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(280): Show | 286 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.5772+1123A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525446 | ||||||
| chr5:71525446
|
A | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5772+1123A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525446 | ||||||
| chr5:71525447
|
CCCCCCAC others(92): Show |
C | 1 | a0001c0001t0002g0036 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5772+1129_5772+122 others(103): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525447 | |||||
| chr5:71525448
|
C | CCCCCACC others(91): Show |
2 | a0002c0002t0001g0153a0026c0040t0001g0152 | 2 | NA18939.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.5772+1144_5772+124 others(102): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525448 | |||||
| chr5:71525463
|
CGGACGGG others(55): Show |
C | 1 | a0002c0002t0005g0183 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.5772+1143_5772+120 others(66): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525463 | |||||
| chr5:71525467
|
CGGGGCGG others(91): Show |
C | 1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5772+1173_5772+127 others(102): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525467 | |||||
| chr5:71525468
|
G | A | 1 | a0006c0028t0021g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5772+1145G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525468 | ||||||
| chr5:71525550
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5772+1227C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525550 | ||||||
| chr5:71525557
|
CTCCCGGA others(42): Show |
C | 117 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(114): Show | 119 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.5772+1242_5772+129 others(53): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525557 | |||||
| chr5:71525565
|
T | C | 129 | a0001c0001t0002g0036a0001c0001t0002g0059a0001c0026t0002g0012others(126): Show | 130 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.5772+1242T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525565 | ||||||
| chr5:71525570
|
C | T | 16 | a0001c0001t0002g0059a0001c0026t0002g0012a0004c0004t0004g0311others(13): Show | 16 | HG01192.hp1 HG01433.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.5772+1247C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525570 | ||||||
| chr5:71525593
|
CCCCCCAA others(41): Show |
C | 2 | a0001c0001t0002g0059a0007c0006t0002g0079 | 2 | HG01192.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.5772+1276_5772+132 others(52): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525593 | |||||
| chr5:71525595
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5772+1272C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525595 | ||||||
| chr5:71525599
|
A | C | 128 | a0001c0001t0002g0036a0001c0026t0002g0012a0002c0002t0001g0132others(125): Show | 129 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.5772+1276A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525599 | ||||||
| chr5:71525606
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5772+1283T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525606 | ||||||
| chr5:71525619
|
C | T | 118 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(115): Show | 120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.5772+1296C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525619 | ||||||
| chr5:71525680
|
C | CG | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+1363dupG | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71525680 | |||||
| chr5:71525681
|
G | A | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5772+1358G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525681 | ||||||
| chr5:71525707
|
C | T | 1 | a0002c0002t0001g0224 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5772+1384C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525707 | ||||||
| chr5:71525716
|
C | T | 1 | a0005c0005t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5772+1393C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525716 | ||||||
| chr5:71525725
|
A | G | 1 | a0005c0005t0001g0236 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5772+1402A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525725 | ||||||
| chr5:71525728
|
C | T | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5772+1405C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525728 | ||||||
| chr5:71525791
|
T | A | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5772+1468T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525791 | ||||||
| chr5:71525798
|
C | T | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5772+1475C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71525798 | ||||||
| chr5:71526016
|
T | C | 1 | a0010c0012t0003g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5772+1693T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526016 | ||||||
| chr5:71526031
|
C | CG | 11 | a0001c0001t0002g0029a0001c0001t0002g0049a0001c0001t0002g0121others(8): Show | 11 | HG00438.hp2 HG01099.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.5772+1712dupG | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526031 | |||||
| chr5:71526058
|
A | G | 1 | a0003c0003t0006g0241 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5772+1735A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526058 | ||||||
| chr5:71526144
|
G | T | 6 | a0003c0003t0001g0238a0003c0003t0001g0245a0003c0003t0001g0246others(3): Show | 6 | NA18942.hp2 NA18943.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.5772+1821G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526144 | ||||||
| chr5:71526277
|
T | TGGCA | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5772+1956_5772+195 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526277 | |||||
| chr5:71526316
|
C | CT | 132 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(129): Show | 134 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.5772+2005dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526316 | |||||
| chr5:71526615
|
C | CA | 19 | a0002c0002t0001g0199a0002c0002t0001g0214a0002c0002t0001g0303others(16): Show | 19 | HG01123.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.5772+2313dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526615 | |||||
| chr5:71526615
|
C | CAAA | 94 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(91): Show | 96 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.5772+2311_5772+231 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526615 | |||||
| chr5:71526615
|
C | CAAAA | 16 | a0001c0001t0002g0015a0001c0001t0002g0030a0001c0001t0002g0035others(13): Show | 16 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.5772+2310_5772+231 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526615 | |||||
| chr5:71526615
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5772+2303_5772+231 others(15): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526615 | |||||
| chr5:71526634
|
A | G | 3 | a0003c0003t0001g0290a0003c0003t0001g0291a0003c0003t0001g0295 | 3 | HG00140.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5772+2311A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526634 | ||||||
| chr5:71526685
|
G | GT | 23 | a0001c0001t0002g0049a0001c0001t0002g0060a0002c0002t0001g0156others(20): Show | 23 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.5772+2381dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71526685 | |||||
| chr5:71526711
|
G | A | 1 | a0005c0005t0001g0235 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5772+2388G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526711 | ||||||
| chr5:71526809
|
T | C | 1 | a0003c0003t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5772+2486T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526809 | ||||||
| chr5:71526995
|
A | T | 1 | a0001c0001t0002g0059 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.5772+2672A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71526995 | ||||||
| chr5:71527094
|
T | A | 1 | a0010c0012t0003g0166 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5772+2771T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527094 | ||||||
| chr5:71527173
|
G | A | 3 | a0003c0003t0001g0266a0003c0003t0001g0267a0003c0003t0001g0273 | 3 | NA18966.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.5772+2850G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527173 | ||||||
| chr5:71527202
|
C | T | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.5772+2879C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527202 | ||||||
| chr5:71527241
|
C | T | 1 | a0011c0011t0001g0184 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.5772+2918C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527241 | ||||||
| chr5:71527242
|
G | A | 7 | a0008c0009t0002g0028a0008c0009t0002g0053a0008c0009t0002g0110others(4): Show | 7 | HG02572.hp2 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.5772+2919G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527242 | ||||||
| chr5:71527248
|
A | G | 99 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(96): Show | 101 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.5772+2925A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527248 | ||||||
| chr5:71527260
|
C | G | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5772+2937C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527260 | ||||||
| chr5:71527674
|
A | G | 1 | a0005c0005t0001g0235 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5772+3351A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527674 | ||||||
| chr5:71527820
|
C | CT | 19 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020others(16): Show | 19 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.5772+3512dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr5 | 71527820 | |||||
| chr5:71527842
|
GA | G | 6 | a0017c0017t0009g0115a0017c0017t0009g0116a0021c0020t0023g0119others(3): Show | 6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5772+3520delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71527842 | ||||||
| chr5:71528156
|
G | C | 1 | a0002c0002t0003g0134 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5772+3833G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71528156 | ||||||
| chr5:71528157
|
C | A | 1 | a0002c0002t0003g0134 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5772+3834C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71528157 | ||||||
| chr5:71528159
|
A | C | 1 | a0002c0002t0003g0134 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5772+3836A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71528159 | ||||||
| chr5:71528339
|
G | A | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5773-3969G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71528339 | ||||||
| chr5:71529528
|
A | G | 8 | a0005c0005t0001g0234a0005c0005t0001g0235a0005c0005t0001g0236others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.5773-2780A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71529528 | ||||||
| chr5:71529558
|
G | T | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5773-2750G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71529558 | ||||||
| chr5:71529561
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5773-2747C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71529561 | ||||||
| chr5:71529894
|
T | C | 1 | a0001c0001t0002g0024 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5773-2414T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71529894 | ||||||
| chr5:71530018
|
A | G | 1 | a0004c0004t0004g0318 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5773-2290A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530018 | ||||||
| chr5:71530052
|
C | T | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(140): Show | 145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.5773-2256C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530052 | ||||||
| chr5:71530224
|
A | C | 1 | a0001c0001t0002g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5773-2084A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530224 | ||||||
| chr5:71530412
|
T | A | 1 | a0001c0001t0002g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5773-1896T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530412 | ||||||
| chr5:71530623
|
G | A | 6 | a0017c0017t0009g0115a0017c0017t0009g0116a0021c0020t0023g0119others(3): Show | 6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5773-1685G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530623 | ||||||
| chr5:71530858
|
G | A | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.5773-1450G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530858 | ||||||
| chr5:71530954
|
G | A | 2 | a0001c0001t0002g0070a0001c0001t0002g0084 | 2 | NA18939.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.5773-1354G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530954 | ||||||
| chr5:71530968
|
G | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0051 | 2 | HG00735.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.5773-1340G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530968 | ||||||
| chr5:71530979
|
C | T | 1 | a0003c0003t0001g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5773-1329C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71530979 | ||||||
| chr5:71531085
|
A | T | 1 | a0006c0028t0021g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5773-1223A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71531085 | ||||||
| chr5:71531303
|
T | A | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.5773-1005T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71531303 | ||||||
| chr5:71531685
|
T | A | 2 | a0002c0002t0001g0146a0002c0002t0001g0181 | 2 | NA18942.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.5773-623T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71531685 | ||||||
| chr5:71531801
|
G | A | 5 | a0006c0007t0002g0106a0006c0007t0002g0107a0006c0007t0002g0108others(2): Show | 5 | HG02896.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.5773-507G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71531801 | ||||||
| chr5:71532053
|
T | C | 1 | a0002c0002t0001g0195 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5773-255T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71532053 | ||||||
| chr5:71532097
|
C | G | 1 | a0002c0002t0001g0198 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.5773-211C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71532097 | ||||||
| chr5:71532106
|
C | T | 1 | a0005c0005t0015g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5773-202C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71532106 | ||||||
| chr5:71532148
|
G | A | 3 | a0001c0001t0002g0034a0001c0001t0002g0039a0001c0001t0020g0052 | 3 | HG01070.hp1 HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.5773-160G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 25/38 | chr5 | 71532148 | ||||||
| chr5:71532464
|
C | T | 1 | a0007c0006t0002g0079 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5892+37C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532464 | ||||||
| chr5:71532579
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5892+152G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532579 | ||||||
| chr5:71532590
|
TTTTG | T | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.5892+173_5892+176d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71532590 | |||||
| chr5:71532792
|
A | G | 2 | a0008c0009t0002g0028a0008c0048t0002g0009 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.5892+365A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532792 | ||||||
| chr5:71532793
|
T | C | 1 | a0003c0003t0001g0274 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5892+366T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532793 | ||||||
| chr5:71532856
|
G | A | 6 | a0009c0008t0002g0007a0009c0008t0002g0090a0009c0008t0007g0095others(3): Show | 6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.5892+429G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71532856 | ||||||
| chr5:71533053
|
T | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(140): Show | 145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.5892+626T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533053 | ||||||
| chr5:71533156
|
A | C | 1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5892+729A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533156 | ||||||
| chr5:71533264
|
A | T | 2 | a0002c0002t0001g0200a0002c0002t0001g0201 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.5892+837A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533264 | ||||||
| chr5:71533462
|
C | T | 2 | a0004c0004t0004g0319a0004c0004t0004g0320 | 2 | NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.5892+1035C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533462 | ||||||
| chr5:71533468
|
A | AT | 102 | a0001c0001t0002g0041a0002c0002t0001g0132a0002c0002t0001g0135others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.5892+1058dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71533468 | |||||
| chr5:71533684
|
G | A | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5892+1257G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533684 | ||||||
| chr5:71533850
|
T | G | 1 | a0001c0001t0022g0013 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5892+1423T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533850 | ||||||
| chr5:71533857
|
C | T | 1 | a0002c0002t0001g0180 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5892+1430C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71533857 | ||||||
| chr5:71534114
|
G | A | 1 | a0005c0005t0001g0299 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5892+1687G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534114 | ||||||
| chr5:71534224
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5892+1797G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534224 | ||||||
| chr5:71534331
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5892+1904C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534331 | ||||||
| chr5:71534496
|
G | GT | 68 | a0001c0001t0020g0052a0002c0002t0001g0135a0002c0002t0001g0140others(65): Show | 69 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.5892+2079dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71534496 | |||||
| chr5:71534504
|
T | G | 7 | a0005c0005t0001g0234a0005c0005t0001g0235a0005c0005t0001g0236others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.5892+2077T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534504 | ||||||
| chr5:71534504
|
T | TG | 3 | a0002c0002t0005g0178a0002c0002t0005g0189a0013c0013t0001g0143 | 3 | HG03927.hp2 NA18963.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.5892+2077_5892+207 others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534504 | ||||||
| chr5:71534702
|
C | T | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.5892+2275C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534702 | ||||||
| chr5:71534704
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5892+2277C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534704 | ||||||
| chr5:71534767
|
G | A | 1 | a0003c0003t0001g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5892+2340G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534767 | ||||||
| chr5:71534871
|
T | C | 1 | a0016c0014t0001g0005 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.5892+2444T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71534871 | ||||||
| chr5:71535039
|
T | G | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5892+2612T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535039 | ||||||
| chr5:71535060
|
C | G | 1 | a0001c0001t0002g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5892+2633C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535060 | ||||||
| chr5:71535128
|
T | G | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5892+2701T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535128 | ||||||
| chr5:71535173
|
T | C | 250 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(247): Show | 253 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.5892+2746T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535173 | ||||||
| chr5:71535202
|
AT | A | 6 | a0001c0001t0002g0019a0001c0001t0002g0070a0001c0001t0002g0125others(3): Show | 6 | HG01169.hp1 HG02965.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.5892+2791delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71535202 | |||||
| chr5:71535263
|
G | A | 1 | a0001c0001t0022g0013 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5892+2836G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535263 | ||||||
| chr5:71535353
|
C | T | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.5892+2926C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535353 | ||||||
| chr5:71535526
|
C | A | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5892+3099C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535526 | ||||||
| chr5:71535527
|
G | A | 1 | a0005c0005t0017g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5892+3100G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535527 | ||||||
| chr5:71535585
|
T | C | 9 | a0007c0006t0002g0017a0007c0006t0002g0042a0007c0006t0002g0043others(6): Show | 9 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.5892+3158T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535585 | ||||||
| chr5:71535686
|
A | T | 1 | a0003c0003t0001g0248 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5892+3259A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535686 | ||||||
| chr5:71535789
|
C | G | 1 | a0003c0003t0001g0265 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5893-3253C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535789 | ||||||
| chr5:71535814
|
C | G | 105 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(102): Show | 106 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.5893-3228C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71535814 | ||||||
| chr5:71536157
|
A | AT | 4 | a0003c0003t0001g0256a0003c0003t0001g0257a0003c0003t0001g0258others(1): Show | 4 | HG00099.hp1 HG01255.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.5893-2878dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71536157 | |||||
| chr5:71536204
|
A | G | 8 | a0005c0005t0001g0234a0005c0005t0001g0235a0005c0005t0001g0236others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.5893-2838A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536204 | ||||||
| chr5:71536371
|
T | C | 1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5893-2671T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536371 | ||||||
| chr5:71536565
|
C | T | 2 | a0006c0007t0002g0103a0006c0007t0002g0105 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5893-2477C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536565 | ||||||
| chr5:71536623
|
C | T | 10 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(7): Show | 10 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.5893-2419C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536623 | ||||||
| chr5:71536702
|
C | T | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5893-2340C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536702 | ||||||
| chr5:71536706
|
T | C | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5893-2336T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536706 | ||||||
| chr5:71536784
|
C | T | 3 | a0016c0014t0001g0004a0016c0014t0001g0005a0022c0019t0024g0118 | 3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5893-2258C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71536784 | ||||||
| chr5:71536996
|
C | CA | 6 | a0017c0017t0009g0115a0017c0017t0009g0116a0021c0020t0023g0119others(3): Show | 6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5893-2045dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71536996 | |||||
| chr5:71537140
|
C | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5893-1902C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537140 | ||||||
| chr5:71537149
|
C | CA | 62 | a0002c0002t0001g0135a0002c0002t0001g0140a0002c0002t0001g0142others(59): Show | 63 | HG00423.hp1 HG00438.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.5893-1870dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71537149 | |||||
| chr5:71537149
|
CA | C | 127 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(124): Show | 129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.5893-1870delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71537149 | |||||
| chr5:71537250
|
G | T | 1 | a0028c0043t0001g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5893-1792G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537250 | ||||||
| chr5:71537317
|
G | T | 8 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(5): Show | 8 | HG02056.hp2 NA18950.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.5893-1725G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537317 | ||||||
| chr5:71537340
|
A | G | 1 | a0003c0003t0001g0267 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.5893-1702A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537340 | ||||||
| chr5:71537415
|
C | T | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5893-1627C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537415 | ||||||
| chr5:71537513
|
T | G | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(140): Show | 145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.5893-1529T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537513 | ||||||
| chr5:71537554
|
G | A | 2 | a0006c0007t0002g0006a0006c0028t0021g0008 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.5893-1488G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537554 | ||||||
| chr5:71537685
|
T | C | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5893-1357T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537685 | ||||||
| chr5:71537743
|
T | A | 1 | a0002c0002t0003g0134 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5893-1299T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71537743 | ||||||
| chr5:71538133
|
C | T | 3 | a0002c0002t0001g0180a0035c0032t0001g0114a0038c0035t0001g0123 | 3 | HG01243.hp2 HG01433.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.5893-909C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538133 | ||||||
| chr5:71538250
|
A | G | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5893-792A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538250 | ||||||
| chr5:71538264
|
G | T | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5893-778G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538264 | ||||||
| chr5:71538316
|
G | A | 1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5893-726G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538316 | ||||||
| chr5:71538435
|
CAT | C | 9 | a0002c0002t0001g0187a0002c0002t0001g0213a0002c0002t0005g0171others(6): Show | 9 | NA18947.hp1 NA18949.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.5893-605_5893-604d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr5 | 71538435 | |||||
| chr5:71538655
|
G | A | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(89): Show | 94 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.5893-387G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538655 | ||||||
| chr5:71538674
|
G | T | 1 | a0003c0003t0001g0305 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5893-368G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538674 | ||||||
| chr5:71538704
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5893-338G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538704 | ||||||
| chr5:71538805
|
A | T | 1 | a0003c0003t0001g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5893-237A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538805 | ||||||
| chr5:71538876
|
A | C | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5893-166A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71538876 | ||||||
| chr5:71539006
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.5893-36G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71539006 | ||||||
| chr5:71539028
|
T | G | 1 | a0003c0003t0001g0271 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5893-14T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 26/38 | chr5 | 71539028 | ||||||
| chr5:71539089
|
T | C | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5929+11T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539089 | ||||||
| chr5:71539099
|
T | C | 104 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(101): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.5929+21T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539099 | ||||||
| chr5:71539126
|
T | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5929+48T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539126 | ||||||
| chr5:71539265
|
G | A | 5 | a0003c0003t0006g0241a0012c0010t0006g0242a0012c0010t0006g0250others(2): Show | 5 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.5929+187G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539265 | ||||||
| chr5:71539379
|
T | G | 1 | a0033c0027t0002g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5930-178T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539379 | ||||||
| chr5:71539380
|
G | C | 1 | a0003c0003t0001g0266 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5930-177G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539380 | ||||||
| chr5:71539474
|
A | C | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5930-83A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 27/38 | chr5 | 71539474 | ||||||
| chr5:71539881
|
TCATGGAA others(10): Show |
T | 7 | a0006c0007t0002g0103a0006c0007t0002g0105a0006c0007t0002g0106others(4): Show | 7 | HG02896.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.6022+255_6022+271d others(19): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr5 | 71539881 | |||||
| chr5:71540074
|
A | G | 1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6022+425A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540074 | ||||||
| chr5:71540180
|
T | C | 257 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(254): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.6022+531T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540180 | ||||||
| chr5:71540279
|
CTTAT | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6022+641_6022+644d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr5 | 71540279 | |||||
| chr5:71540298
|
C | T | 4 | a0008c0009t0002g0110a0008c0009t0002g0111a0008c0009t0002g0112others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.6022+649C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540298 | ||||||
| chr5:71540321
|
A | G | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6022+672A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540321 | ||||||
| chr5:71540576
|
T | C | 257 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(254): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.6023-878T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540576 | ||||||
| chr5:71540668
|
C | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6023-786C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71540668 | ||||||
| chr5:71541131
|
G | GCTGT | 257 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(254): Show | 260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.6023-320_6023-317d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr5 | 71541131 | |||||
| chr5:71541180
|
G | T | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.6023-274G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71541180 | ||||||
| chr5:71541315
|
A | C | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6023-139A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 28/38 | chr5 | 71541315 | ||||||
| chr5:71541762
|
G | A | 1 | a0003c0003t0001g0280 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6251+80G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 29/38 | chr5 | 71541762 | ||||||
| chr5:71542449
|
C | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0128 | 2 | NA18950.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.6412+184C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542449 | ||||||
| chr5:71542565
|
C | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6412+300C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542565 | ||||||
| chr5:71542614
|
G | A | 1 | a0002c0002t0001g0197 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.6412+349G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542614 | ||||||
| chr5:71542701
|
C | CAT | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6412+451_6412+452d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr5 | 71542701 | |||||
| chr5:71542701
|
C | CATATAT | 11 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(8): Show | 11 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.6412+447_6412+452d others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | INFO_REALIGN_3_PRIME | chr5 | 71542701 | |||||
| chr5:71542750
|
C | A | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.6412+485C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542750 | ||||||
| chr5:71542870
|
A | T | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6412+605A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71542870 | ||||||
| chr5:71543220
|
C | T | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.6412+955C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543220 | ||||||
| chr5:71543256
|
T | C | 1 | a0040c0045t0002g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6412+991T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543256 | ||||||
| chr5:71543377
|
C | T | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6413-980C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543377 | ||||||
| chr5:71543429
|
T | A | 3 | a0003c0003t0001g0255a0003c0003t0001g0286a0003c0049t0001g0269 | 3 | HG02559.hp1 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6413-928T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543429 | ||||||
| chr5:71543555
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.6413-802C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543555 | ||||||
| chr5:71543724
|
G | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6413-633G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543724 | ||||||
| chr5:71543731
|
C | T | 255 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(252): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.6413-626C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543731 | ||||||
| chr5:71543851
|
A | G | 248 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.6413-506A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71543851 | ||||||
| chr5:71544169
|
G | C | 255 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(252): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.6413-188G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 30/38 | chr5 | 71544169 | ||||||
| chr5:71544606
|
A | G | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(134): Show | 139 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.6563+99A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544606 | ||||||
| chr5:71544695
|
C | T | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6563+188C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544695 | ||||||
| chr5:71544759
|
AGTT | A | 3 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026 | 3 | HG00673.hp2 HG02523.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.6563+255_6563+257d others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544759 | |||||
| chr5:71544780
|
C | T | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.6564-259C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544780 | ||||||
| chr5:71544812
|
G | A | 1 | a0001c0022t0002g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6564-227G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544812 | ||||||
| chr5:71544858
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.6564-181C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544858 | ||||||
| chr5:71544859
|
G | A | 3 | a0011c0011t0001g0184a0011c0011t0001g0185a0011c0011t0001g0202 | 3 | HG01975.hp1 HG01981.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.6564-180G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544859 | ||||||
| chr5:71544879
|
C | CA | 24 | a0002c0002t0001g0163a0002c0002t0001g0211a0003c0003t0001g0244others(21): Show | 24 | HG00621.hp1 HG00735.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.6564-133dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544879 | |||||
| chr5:71544879
|
C | CAA | 7 | a0003c0003t0001g0275a0003c0003t0001g0308a0003c0003t0018g0307others(4): Show | 7 | HG00642.hp2 HG00733.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.6564-134_6564-133d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544879 | |||||
| chr5:71544879
|
CA | C | 76 | a0002c0002t0001g0132a0002c0002t0001g0136a0002c0002t0001g0142others(73): Show | 77 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.6564-133delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544879 | |||||
| chr5:71544879
|
CAAAAAAA others(3): Show |
C | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6564-142_6564-133d others(12): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544879 | |||||
| chr5:71544904
|
A | AAAAAAG | 9 | a0001c0001t0002g0038a0001c0026t0002g0012a0004c0004t0004g0312others(6): Show | 9 | HG01943.hp1 HG01978.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.6564-133_6564-132i others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544904 | |||||
| chr5:71544904
|
A | AAAAAG | 25 | a0001c0001t0002g0022a0001c0001t0002g0030a0001c0001t0002g0036others(22): Show | 25 | HG00597.hp1 HG00621.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.6564-133_6564-132i others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544904 | |||||
| chr5:71544904
|
A | AAAAG | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.6564-133_6564-132i others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544904 | |||||
| chr5:71544904
|
A | AAAG | 7 | a0001c0001t0002g0019a0001c0001t0002g0021a0006c0024t0002g0104others(4): Show | 7 | HG01167.hp1 HG02896.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.6564-134_6564-132d others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr5 | 71544904 | |||||
| chr5:71544904
|
A | G | 6 | a0001c0001t0002g0075a0001c0001t0002g0121a0004c0004t0004g0311others(3): Show | 6 | HG00438.hp2 HG02027.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.6564-135A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544904 | ||||||
| chr5:71544907
|
G | A | 1 | a0003c0003t0001g0280 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6564-132G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 31/38 | chr5 | 71544907 | ||||||
| chr5:71545337
|
C | A | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6744+118C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545337 | ||||||
| chr5:71545373
|
C | T | 2 | a0005c0005t0001g0233a0005c0005t0015g0310 | 2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6744+154C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545373 | ||||||
| chr5:71545528
|
G | A | 2 | a0001c0001t0002g0074a0001c0001t0019g0016 | 2 | HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.6744+309G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545528 | ||||||
| chr5:71545598
|
T | A | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.6744+379T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545598 | ||||||
| chr5:71545669
|
A | G | 6 | a0003c0003t0001g0231a0003c0003t0001g0240a0003c0003t0001g0255others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.6744+450A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545669 | ||||||
| chr5:71545773
|
G | A | 1 | a0001c0001t0019g0016 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6744+554G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545773 | ||||||
| chr5:71545780
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6744+561G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545780 | ||||||
| chr5:71545840
|
T | TA | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6744+634dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71545840 | |||||
| chr5:71545859
|
G | C | 6 | a0017c0017t0009g0115a0017c0017t0009g0116a0021c0020t0023g0119others(3): Show | 6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.6744+640G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71545859 | ||||||
| chr5:71546237
|
A | G | 9 | a0006c0007t0002g0006a0006c0007t0002g0103a0006c0007t0002g0105others(6): Show | 9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.6744+1018A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546237 | ||||||
| chr5:71546249
|
C | A | 111 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(108): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.6744+1030C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546249 | ||||||
| chr5:71546269
|
A | G | 1 | a0001c0001t0019g0016 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6744+1050A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546269 | ||||||
| chr5:71546276
|
A | G | 1 | a0004c0004t0010g0321 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6744+1057A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546276 | ||||||
| chr5:71546500
|
C | G | 1 | a0004c0004t0004g0312 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.6744+1281C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546500 | ||||||
| chr5:71546594
|
G | T | 3 | a0003c0003t0001g0243a0003c0003t0001g0249a0003c0003t0001g0270 | 3 | NA18959.hp1 NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.6744+1375G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546594 | ||||||
| chr5:71546596
|
C | T | 1 | a0009c0008t0002g0090 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6744+1377C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546596 | ||||||
| chr5:71546608
|
A | C | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6744+1389A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546608 | ||||||
| chr5:71546617
|
C | CA | 52 | a0003c0003t0001g0231a0003c0003t0001g0238a0003c0003t0001g0240others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.6744+1426dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | |||||
| chr5:71546617
|
CA | C | 84 | a0002c0002t0001g0135a0002c0002t0001g0140a0002c0002t0001g0145others(81): Show | 85 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.6744+1426delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | |||||
| chr5:71546617
|
CAA | C | 44 | a0001c0022t0002g0081a0002c0002t0001g0132a0002c0002t0001g0136others(41): Show | 44 | HG00609.hp1 HG00642.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.6744+1425_6744+142 others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | |||||
| chr5:71546617
|
CAAA | C | 76 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0018others(73): Show | 76 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.6744+1424_6744+142 others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | |||||
| chr5:71546617
|
CAAAA | C | 40 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0020others(37): Show | 42 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.6744+1423_6744+142 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546617 | |||||
| chr5:71546698
|
G | A | 1 | a0017c0017t0009g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6744+1479G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546698 | ||||||
| chr5:71546782
|
G | T | 1 | a0024c0042t0001g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6744+1563G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546782 | ||||||
| chr5:71546850
|
CT | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6744+1638delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr5 | 71546850 | |||||
| chr5:71546935
|
T | C | 5 | a0001c0001t0002g0002a0001c0001t0002g0088a0001c0001t0002g0089others(2): Show | 6 | HG02155.hp2 NA18989.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.6744+1716T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71546935 | ||||||
| chr5:71547002
|
C | T | 111 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(108): Show | 113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.6745-1680C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547002 | ||||||
| chr5:71547088
|
A | G | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6745-1594A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547088 | ||||||
| chr5:71547144
|
C | T | 12 | a0003c0003t0001g0232a0003c0003t0001g0274a0003c0003t0001g0275others(9): Show | 12 | HG02055.hp1 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.6745-1538C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547144 | ||||||
| chr5:71547165
|
A | T | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.6745-1517A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547165 | ||||||
| chr5:71547279
|
A | G | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6745-1403A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547279 | ||||||
| chr5:71547284
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6745-1398C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547284 | ||||||
| chr5:71547533
|
T | G | 1 | a0007c0006t0002g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6745-1149T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547533 | ||||||
| chr5:71547536
|
G | T | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.6745-1146G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547536 | ||||||
| chr5:71547579
|
C | T | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6745-1103C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547579 | ||||||
| chr5:71547676
|
C | A | 1 | a0001c0001t0002g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6745-1006C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547676 | ||||||
| chr5:71547763
|
C | T | 1 | a0002c0039t0001g0207 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.6745-919C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547763 | ||||||
| chr5:71547823
|
C | G | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6745-859C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547823 | ||||||
| chr5:71547882
|
A | C | 1 | a0002c0002t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6745-800A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547882 | ||||||
| chr5:71547952
|
C | A | 1 | a0001c0001t0002g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.6745-730C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71547952 | ||||||
| chr5:71548048
|
C | G | 2 | a0001c0001t0002g0014a0001c0001t0002g0040 | 2 | HG01109.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.6745-634C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71548048 | ||||||
| chr5:71548164
|
C | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6745-518C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71548164 | ||||||
| chr5:71548284
|
A | G | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6745-398A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71548284 | ||||||
| chr5:71548671
|
T | C | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6745-11T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 32/38 | chr5 | 71548671 | ||||||
| chr5:71548868
|
G | A | 2 | a0021c0020t0023g0119a0041c0047t0001g0228 | 2 | HG00642.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6808+123G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71548868 | ||||||
| chr5:71549100
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6809-320C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549100 | ||||||
| chr5:71549115
|
G | C | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6809-305G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549115 | ||||||
| chr5:71549163
|
A | G | 1 | a0003c0003t0001g0271 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6809-257A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549163 | ||||||
| chr5:71549236
|
T | TG | 3 | a0016c0014t0001g0004a0016c0014t0001g0005a0022c0019t0024g0118 | 3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6809-184_6809-183i others(3): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549236 | ||||||
| chr5:71549243
|
C | A | 3 | a0002c0002t0001g0145a0002c0002t0001g0156a0002c0002t0001g0180 | 3 | HG01433.hp2 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.6809-177C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549243 | ||||||
| chr5:71549244
|
G | A | 1 | a0004c0004t0004g0313 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.6809-176G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549244 | ||||||
| chr5:71549313
|
T | C | 1 | a0001c0001t0002g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6809-107T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 33/38 | chr5 | 71549313 | ||||||
| chr5:71549986
|
T | C | 118 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(115): Show | 120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.6995+380T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71549986 | ||||||
| chr5:71550222
|
C | G | 6 | a0017c0017t0009g0115a0017c0017t0009g0116a0021c0020t0023g0119others(3): Show | 6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.6995+616C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550222 | ||||||
| chr5:71550285
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6995+679C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550285 | ||||||
| chr5:71550376
|
G | A | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6995+770G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550376 | ||||||
| chr5:71550385
|
A | G | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.6995+779A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550385 | ||||||
| chr5:71550393
|
C | T | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6995+787C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550393 | ||||||
| chr5:71550446
|
G | A | 2 | a0002c0041t0001g0144a0042c0052t0001g0226 | 2 | NA18957.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.6995+840G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550446 | ||||||
| chr5:71550457
|
TA | T | 141 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(138): Show | 143 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.6995+860delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71550457 | |||||
| chr5:71550466
|
AT | A | 104 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(101): Show | 105 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.6995+870delT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71550466 | |||||
| chr5:71550572
|
G | C | 1 | a0002c0002t0001g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6995+966G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550572 | ||||||
| chr5:71550865
|
T | C | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(134): Show | 139 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.6995+1259T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550865 | ||||||
| chr5:71550997
|
C | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6995+1391C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71550997 | ||||||
| chr5:71551097
|
GTTTA | G | 232 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(229): Show | 235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.6995+1519_6995+152 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551097 | |||||
| chr5:71551097
|
GTTTATTT others(1): Show |
G | 19 | a0001c0001t0002g0060a0004c0004t0004g0311a0004c0004t0004g0312others(16): Show | 19 | HG00597.hp1 HG00642.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.6995+1515_6995+152 others(12): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551097 | |||||
| chr5:71551230
|
T | G | 118 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(115): Show | 120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.6995+1624T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551230 | ||||||
| chr5:71551404
|
G | T | 127 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(124): Show | 129 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.6996-1712G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551404 | ||||||
| chr5:71551564
|
C | A | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6996-1552C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551564 | ||||||
| chr5:71551587
|
G | A | 1 | a0035c0032t0001g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6996-1529G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551587 | ||||||
| chr5:71551653
|
G | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6996-1463G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551653 | ||||||
| chr5:71551665
|
TTCACTTC others(30): Show |
T | 1 | a0001c0001t0002g0063 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.6996-1419_6996-138 others(41): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551665 | |||||
| chr5:71551720
|
C | T | 1 | a0002c0002t0001g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6996-1396C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551720 | ||||||
| chr5:71551752
|
C | T | 1 | a0003c0003t0001g0271 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6996-1364C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551752 | ||||||
| chr5:71551781
|
C | T | 1 | a0003c0003t0001g0268 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6996-1335C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551781 | ||||||
| chr5:71551801
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6996-1315C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551801 | ||||||
| chr5:71551875
|
C | T | 1 | a0011c0011t0001g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.6996-1241C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551875 | ||||||
| chr5:71551893
|
A | AGGCGGGG others(42): Show |
2 | a0011c0011t0001g0173a0011c0011t0014g0147 | 2 | HG00642.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.6996-1174_6996-112 others(53): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551893 | |||||
| chr5:71551893
|
A | G | 2 | a0001c0022t0002g0081a0002c0002t0001g0301 | 2 | HG03942.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.6996-1223A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551893 | ||||||
| chr5:71551893
|
AGGCGGGG others(42): Show |
A | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6996-1174_6996-112 others(53): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71551893 | |||||
| chr5:71551896
|
C | T | 1 | a0016c0014t0001g0005 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6996-1220C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551896 | ||||||
| chr5:71551925
|
G | A | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.6996-1191G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551925 | ||||||
| chr5:71551956
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6996-1160C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551956 | ||||||
| chr5:71551996
|
A | G | 255 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(252): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.6996-1120A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71551996 | ||||||
| chr5:71552036
|
G | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6996-1080G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552036 | ||||||
| chr5:71552103
|
C | T | 6 | a0009c0008t0002g0007a0009c0008t0002g0090a0009c0008t0007g0095others(3): Show | 6 | HG01167.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.6996-1013C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552103 | ||||||
| chr5:71552108
|
C | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6996-1008C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552108 | ||||||
| chr5:71552126
|
G | GCTCCTCA others(33): Show |
134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.6996-968_6996-967i others(42): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71552126 | |||||
| chr5:71552265
|
G | A | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6996-851G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552265 | ||||||
| chr5:71552413
|
C | T | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6996-703C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552413 | ||||||
| chr5:71552420
|
C | T | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6996-696C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552420 | ||||||
| chr5:71552502
|
C | T | 1 | a0002c0002t0001g0172 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.6996-614C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552502 | ||||||
| chr5:71552568
|
G | A | 1 | a0003c0003t0001g0278 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6996-548G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552568 | ||||||
| chr5:71552603
|
C | T | 3 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026 | 3 | HG00673.hp2 HG02523.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.6996-513C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552603 | ||||||
| chr5:71552604
|
G | A | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6996-512G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552604 | ||||||
| chr5:71552679
|
G | A | 120 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.6996-437G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552679 | ||||||
| chr5:71552687
|
T | C | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.6996-429T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552687 | ||||||
| chr5:71552690
|
C | T | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6996-426C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552690 | ||||||
| chr5:71552703
|
G | A | 1 | a0016c0014t0001g0005 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6996-413G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552703 | ||||||
| chr5:71552718
|
G | A | 9 | a0006c0007t0002g0006a0006c0007t0002g0103a0006c0007t0002g0105others(6): Show | 9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.6996-398G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552718 | ||||||
| chr5:71552736
|
G | C | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6996-380G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552736 | ||||||
| chr5:71552753
|
G | A | 1 | a0002c0002t0001g0151 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6996-363G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552753 | ||||||
| chr5:71552757
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6996-359C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552757 | ||||||
| chr5:71552801
|
G | A | 101 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(98): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.6996-315G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552801 | ||||||
| chr5:71552816
|
G | C | 67 | a0002c0002t0001g0135a0002c0002t0001g0140a0002c0002t0001g0142others(64): Show | 68 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.6996-300G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552816 | ||||||
| chr5:71552834
|
GGGGAGA | G | 5 | a0010c0012t0003g0148a0010c0012t0003g0165a0010c0012t0003g0166others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.6996-266_6996-261d others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr5 | 71552834 | |||||
| chr5:71552856
|
T | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.6996-260T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552856 | ||||||
| chr5:71552879
|
C | T | 255 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(252): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.6996-237C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552879 | ||||||
| chr5:71552925
|
A | G | 1 | a0024c0042t0001g0182 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6996-191A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552925 | ||||||
| chr5:71552955
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.6996-161G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71552955 | ||||||
| chr5:71553012
|
A | T | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6996-104A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 34/38 | chr5 | 71553012 | ||||||
| chr5:71553405
|
A | T | 10 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020others(7): Show | 10 | HG01167.hp1 HG02015.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.7200+85A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553405 | ||||||
| chr5:71553481
|
T | C | 6 | a0017c0017t0009g0115a0017c0017t0009g0116a0021c0020t0023g0119others(3): Show | 6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.7200+161T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553481 | ||||||
| chr5:71553570
|
A | G | 3 | a0016c0014t0001g0004a0016c0014t0001g0005a0022c0019t0024g0118 | 3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7200+250A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553570 | ||||||
| chr5:71553591
|
A | G | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7200+271A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553591 | ||||||
| chr5:71553613
|
A | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7200+293A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553613 | ||||||
| chr5:71553639
|
A | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7200+319A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553639 | ||||||
| chr5:71553712
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.7200+392A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553712 | ||||||
| chr5:71553719
|
C | T | 255 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(252): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.7200+399C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553719 | ||||||
| chr5:71553750
|
C | G | 1 | a0005c0005t0015g0310 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7200+430C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553750 | ||||||
| chr5:71553766
|
C | A | 1 | a0002c0002t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7200+446C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553766 | ||||||
| chr5:71553788
|
T | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(140): Show | 145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.7200+468T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553788 | ||||||
| chr5:71553852
|
T | A | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7200+532T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553852 | ||||||
| chr5:71553868
|
G | A | 1 | a0002c0002t0001g0213 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.7200+548G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71553868 | ||||||
| chr5:71554055
|
T | G | 9 | a0002c0002t0003g0134a0002c0002t0003g0162a0002c0002t0003g0174others(6): Show | 9 | HG00423.hp1 HG00609.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.7200+735T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554055 | ||||||
| chr5:71554085
|
C | G | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7200+765C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554085 | ||||||
| chr5:71554255
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.7200+935T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554255 | ||||||
| chr5:71554303
|
A | G | 120 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(117): Show | 122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.7200+983A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554303 | ||||||
| chr5:71554766
|
A | AT | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7200+1452dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr5 | 71554766 | |||||
| chr5:71554908
|
C | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7200+1588C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71554908 | ||||||
| chr5:71555058
|
C | T | 1 | a0017c0017t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.7200+1738C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555058 | ||||||
| chr5:71555162
|
C | T | 2 | a0004c0004t0010g0321a0004c0004t0010g0322 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.7201-1724C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555162 | ||||||
| chr5:71555261
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.7201-1625G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555261 | ||||||
| chr5:71555467
|
TTCTC | T | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.7201-1416_7201-141 others(8): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr5 | 71555467 | |||||
| chr5:71555627
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7201-1259C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555627 | ||||||
| chr5:71555628
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.7201-1258G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555628 | ||||||
| chr5:71555676
|
T | A | 1 | a0003c0003t0006g0241 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7201-1210T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555676 | ||||||
| chr5:71555690
|
C | T | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7201-1196C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555690 | ||||||
| chr5:71555705
|
A | C | 308 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(305): Show | 311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.7201-1181A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555705 | ||||||
| chr5:71555943
|
A | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7201-943A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555943 | ||||||
| chr5:71555944
|
C | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.7201-942C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71555944 | ||||||
| chr5:71555959
|
CAGCATAA others(35): Show |
C | 4 | a0002c0002t0003g0134a0002c0002t0003g0174a0002c0002t0012g0157others(1): Show | 4 | HG00738.hp1 HG01496.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.7201-925_7201-884d others(44): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr5 | 71555959 | |||||
| chr5:71556034
|
GTCTT | G | 5 | a0003c0003t0006g0241a0012c0010t0006g0242a0012c0010t0006g0250others(2): Show | 5 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.7201-848_7201-845d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr5 | 71556034 | |||||
| chr5:71556087
|
T | C | 103 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(100): Show | 104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.7201-799T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556087 | ||||||
| chr5:71556382
|
T | C | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7201-504T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556382 | ||||||
| chr5:71556732
|
A | G | 1 | a0003c0003t0006g0241 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7201-154A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556732 | ||||||
| chr5:71556744
|
G | T | 1 | a0028c0043t0001g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7201-142G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556744 | ||||||
| chr5:71556784
|
G | A | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(118): Show | 123 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.7201-102G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556784 | ||||||
| chr5:71556850
|
A | C | 1 | a0002c0002t0001g0216 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7201-36A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 35/38 | chr5 | 71556850 | ||||||
| chr5:71556947
|
A | C | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7240+22A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71556947 | ||||||
| chr5:71557080
|
A | G | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7240+155A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557080 | ||||||
| chr5:71557195
|
A | G | 248 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.7240+270A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557195 | ||||||
| chr5:71557219
|
G | A | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7240+294G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557219 | ||||||
| chr5:71557231
|
C | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7240+306C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557231 | ||||||
| chr5:71557235
|
T | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7240+310T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557235 | ||||||
| chr5:71557315
|
C | A | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7240+390C>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557315 | ||||||
| chr5:71557375
|
A | AT | 23 | a0003c0003t0001g0255a0003c0003t0001g0258a0003c0003t0001g0261others(20): Show | 23 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.7240+477dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | |||||
| chr5:71557375
|
A | ATT | 14 | a0001c0001t0002g0024a0004c0004t0004g0312a0004c0004t0004g0313others(11): Show | 14 | HG01243.hp2 HG01433.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.7240+476_7240+477d others(4): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | |||||
| chr5:71557375
|
A | ATTT | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0015others(87): Show | 92 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.7240+475_7240+477d others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | |||||
| chr5:71557375
|
A | ATTTT | 26 | a0001c0001t0002g0014a0001c0001t0002g0029a0001c0001t0002g0030others(23): Show | 26 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.7240+474_7240+477d others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | |||||
| chr5:71557375
|
A | ATTTTT | 8 | a0006c0007t0002g0103a0006c0007t0002g0105a0006c0007t0002g0106others(5): Show | 8 | HG02258.hp1 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.7240+473_7240+477d others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | |||||
| chr5:71557375
|
ATTTTTTT others(4): Show |
A | 3 | a0002c0002t0001g0163a0002c0002t0003g0206a0011c0011t0001g0184 | 3 | HG01981.hp1 NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.7240+467_7240+477d others(13): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | |||||
| chr5:71557375
|
ATTTTTTT others(5): Show |
A | 99 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(96): Show | 100 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.7240+466_7240+477d others(14): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71557375 | |||||
| chr5:71557415
|
C | T | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7240+490C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557415 | ||||||
| chr5:71557424
|
A | G | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.7240+499A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557424 | ||||||
| chr5:71557425
|
C | T | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.7240+500C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557425 | ||||||
| chr5:71557429
|
G | A | 134 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.7240+504G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557429 | ||||||
| chr5:71557494
|
C | T | 1 | a0002c0002t0003g0174 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7240+569C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557494 | ||||||
| chr5:71557619
|
C | T | 2 | a0017c0017t0009g0115a0017c0017t0009g0116 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.7240+694C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557619 | ||||||
| chr5:71557647
|
G | A | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7240+722G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557647 | ||||||
| chr5:71557654
|
GTAGAGAC others(60): Show |
G | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7240+730_7240+796d others(69): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557654 | ||||||
| chr5:71557945
|
A | G | 9 | a0002c0002t0003g0134a0002c0002t0003g0162a0002c0002t0003g0174others(6): Show | 9 | HG00423.hp1 HG00609.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.7240+1020A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71557945 | ||||||
| chr5:71558016
|
T | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7240+1091T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558016 | ||||||
| chr5:71558051
|
G | A | 12 | a0004c0004t0004g0311a0004c0004t0004g0312a0004c0004t0004g0313others(9): Show | 12 | HG01433.hp1 HG01943.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.7240+1126G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558051 | ||||||
| chr5:71558169
|
G | A | 102 | a0002c0002t0001g0132a0002c0002t0001g0135a0002c0002t0001g0136others(99): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.7240+1244G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558169 | ||||||
| chr5:71558272
|
TG | T | 245 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(242): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.7240+1349delG | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71558272 | |||||
| chr5:71558342
|
C | T | 10 | a0001c0001t0002g0049a0007c0006t0002g0017a0007c0006t0002g0042others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.7240+1417C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558342 | ||||||
| chr5:71558352
|
T | G | 1 | a0002c0002t0001g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.7240+1427T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558352 | ||||||
| chr5:71558421
|
G | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7240+1496G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558421 | ||||||
| chr5:71558441
|
G | A | 2 | a0012c0010t0006g0250a0012c0010t0006g0306 | 2 | HG00741.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.7240+1516G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558441 | ||||||
| chr5:71558462
|
C | T | 2 | a0004c0004t0010g0321a0004c0004t0010g0322 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.7241-1520C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558462 | ||||||
| chr5:71558541
|
C | T | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7241-1441C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558541 | ||||||
| chr5:71558690
|
G | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7241-1292G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558690 | ||||||
| chr5:71558715
|
A | G | 1 | a0040c0045t0002g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7241-1267A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558715 | ||||||
| chr5:71558782
|
C | T | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7241-1200C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558782 | ||||||
| chr5:71558820
|
C | CT | 3 | a0005c0005t0001g0235a0005c0005t0001g0236a0005c0005t0001g0237 | 3 | HG01884.hp2 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.7241-1161dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71558820 | |||||
| chr5:71558832
|
CA | C | 120 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(117): Show | 122 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.7241-1138delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr5 | 71558832 | |||||
| chr5:71558836
|
A | C | 1 | a0005c0005t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7241-1146A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558836 | ||||||
| chr5:71558837
|
A | C | 6 | a0017c0017t0009g0115a0017c0017t0009g0116a0021c0020t0023g0119others(3): Show | 6 | HG00642.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.7241-1145A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558837 | ||||||
| chr5:71558842
|
A | C | 1 | a0002c0002t0001g0160 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.7241-1140A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558842 | ||||||
| chr5:71558897
|
T | C | 1 | a0042c0052t0001g0226 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7241-1085T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71558897 | ||||||
| chr5:71559056
|
A | C | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7241-926A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559056 | ||||||
| chr5:71559157
|
A | G | 118 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(115): Show | 120 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.7241-825A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559157 | ||||||
| chr5:71559279
|
C | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7241-703C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559279 | ||||||
| chr5:71559293
|
C | G | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.7241-689C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559293 | ||||||
| chr5:71559666
|
T | C | 1 | a0041c0047t0001g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7241-316T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 36/38 | chr5 | 71559666 | ||||||
| chr5:71560317
|
T | C | 2 | a0035c0032t0001g0114a0038c0035t0001g0123 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7496+80T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560317 | ||||||
| chr5:71560343
|
A | G | 1 | a0022c0019t0024g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7496+106A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560343 | ||||||
| chr5:71560546
|
T | C | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.7496+309T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560546 | ||||||
| chr5:71560551
|
A | C | 119 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(116): Show | 121 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.7496+314A>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560551 | ||||||
| chr5:71560757
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7496+520C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560757 | ||||||
| chr5:71560836
|
T | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(140): Show | 145 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.7496+599T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560836 | ||||||
| chr5:71560881
|
A | G | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7496+644A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71560881 | ||||||
| chr5:71561103
|
G | C | 2 | a0005c0005t0001g0233a0005c0005t0015g0310 | 2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7496+866G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561103 | ||||||
| chr5:71561349
|
C | T | 2 | a0001c0001t0002g0078a0022c0019t0024g0118 | 2 | HG02258.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.7497-925C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561349 | ||||||
| chr5:71561389
|
G | T | 1 | a0003c0003t0001g0253 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.7497-885G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561389 | ||||||
| chr5:71561405
|
ATAAAT | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0088a0001c0001t0002g0089others(2): Show | 6 | HG02155.hp2 NA18989.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.7497-864_7497-860d others(7): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71561405 | |||||
| chr5:71561487
|
T | C | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7497-787T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561487 | ||||||
| chr5:71561507
|
G | A | 99 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(96): Show | 101 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.7497-767G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561507 | ||||||
| chr5:71561566
|
G | A | 255 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(252): Show | 258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.7497-708G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561566 | ||||||
| chr5:71561651
|
C | T | 1 | a0021c0020t0023g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.7497-623C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71561651 | ||||||
| chr5:71562036
|
A | G | 9 | a0006c0007t0002g0006a0006c0007t0002g0103a0006c0007t0002g0105others(6): Show | 9 | HG02895.hp2 HG02896.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.7497-238A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562036 | ||||||
| chr5:71562081
|
A | G | 3 | a0005c0005t0001g0235a0005c0005t0001g0236a0005c0005t0001g0237 | 3 | HG01884.hp2 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.7497-193A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562081 | ||||||
| chr5:71562095
|
G | C | 3 | a0016c0014t0001g0004a0016c0014t0001g0005a0022c0019t0024g0118 | 3 | HG00733.hp1 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7497-179G>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562095 | ||||||
| chr5:71562146
|
C | T | 3 | a0002c0002t0001g0145a0002c0002t0001g0156a0002c0002t0001g0180 | 3 | HG01433.hp2 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.7497-128C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562146 | ||||||
| chr5:71562195
|
C | CA | 26 | a0002c0002t0001g0197a0002c0002t0001g0211a0002c0002t0001g0227others(23): Show | 26 | HG00673.hp1 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.7497-51dupA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71562195 | |||||
| chr5:71562195
|
CA | C | 39 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020others(36): Show | 39 | HG00597.hp1 HG01433.hp1 HG01943.hp1 others(36): Show |
intron_variant | MODIFIER | c.7497-51delA | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71562195 | |||||
| chr5:71562195
|
CAA | C | 99 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(96): Show | 101 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.7497-52_7497-51del others(2): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71562195 | |||||
| chr5:71562195
|
CAAAAAAA others(3): Show |
C | 10 | a0002c0002t0003g0134a0002c0002t0003g0162a0002c0002t0003g0174others(7): Show | 10 | HG00423.hp1 HG00609.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.7497-60_7497-51del others(10): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr5 | 71562195 | |||||
| chr5:71562262
|
T | C | 1 | a0003c0003t0001g0295 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.7497-12T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 37/38 | chr5 | 71562262 | ||||||
| chr5:71562555
|
G | A | 1 | a0002c0002t0001g0151 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.7743+35G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71562555 | ||||||
| chr5:71562659
|
G | A | 1 | a0009c0008t0007g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7743+139G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71562659 | ||||||
| chr5:71562773
|
A | G | 1 | a0007c0006t0002g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.7743+253A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71562773 | ||||||
| chr5:71562941
|
T | G | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7743+421T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71562941 | ||||||
| chr5:71563078
|
T | G | 1 | a0002c0002t0001g0302 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.7743+558T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563078 | ||||||
| chr5:71563140
|
G | GT | 5 | a0001c0001t0002g0102a0002c0002t0001g0163a0002c0002t0001g0213others(2): Show | 5 | HG02074.hp2 NA18947.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.7743+628dupT | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr5 | 71563140 | |||||
| chr5:71563156
|
T | C | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7743+636T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563156 | ||||||
| chr5:71563260
|
G | T | 1 | a0002c0002t0003g0161 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.7743+740G>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563260 | ||||||
| chr5:71563267
|
C | T | 1 | a0033c0027t0002g0011 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.7743+747C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563267 | ||||||
| chr5:71563344
|
C | T | 1 | a0001c0026t0002g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7743+824C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563344 | ||||||
| chr5:71563363
|
T | G | 135 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(132): Show | 137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.7743+843T>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563363 | ||||||
| chr5:71563723
|
G | A | 2 | a0004c0004t0010g0321a0004c0004t0010g0322 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.7744-1031G>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563723 | ||||||
| chr5:71563836
|
C | T | 2 | a0016c0014t0001g0004a0016c0014t0001g0005 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7744-918C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563836 | ||||||
| chr5:71563870
|
C | G | 2 | a0001c0001t0002g0038a0001c0001t0002g0092 | 2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.7744-884C>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71563870 | ||||||
| chr5:71564155
|
A | G | 2 | a0003c0003t0001g0260a0018c0051t0001g0263 | 2 | HG01069.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7744-599A>G | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564155 | ||||||
| chr5:71564211
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0127 | 2 | NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.7744-543C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564211 | ||||||
| chr5:71564215
|
C | T | 1 | a0003c0003t0013g0251 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.7744-539C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564215 | ||||||
| chr5:71564236
|
C | T | 1 | a0039c0031t0016g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7744-518C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564236 | ||||||
| chr5:71564252
|
A | T | 2 | a0014c0015t0001g0221a0014c0015t0001g0223 | 2 | NA18974.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.7744-502A>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564252 | ||||||
| chr5:71564329
|
A | ATTC | 288 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(285): Show | 291 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.7744-423_7744-422i others(5): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr5 | 71564329 | |||||
| chr5:71564357
|
T | TTTAA | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7744-394_7744-393i others(6): Show |
BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr5 | 71564357 | |||||
| chr5:71564438
|
T | A | 1 | a0038c0035t0001g0123 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7744-316T>A | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564438 | ||||||
| chr5:71564656
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.7744-98C>T | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564656 | ||||||
| chr5:71564666
|
T | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0014others(130): Show | 135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.7744-88T>C | BDP1 | ENSG00000145734.20 | transcript | ENST00000358731.9 | protein_coding | 38/38 | chr5 | 71564666 |