Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 340706 |
| ensemblid | ENSG00000165816.13 |
| hgncid | 24709 |
| symbol | VWA2 |
| name | von Willebrand factor A domain containing 2 |
| refseq_nuc | NM_001272046.2 |
| refseq_prot | NP_001258975.1 |
| ensembl_nuc | ENST00000392982.8 |
| ensembl_prot | ENSP00000376708.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 114239254 |
| end | 114294489 |
| strand | + |
| ver | v1.2 |
| region | chr10:114239254-114294489 |
| region5000 | chr10:114234254-114299489 |
| regionname0 | VWA2_chr10_114239254_114294489 |
| regionname5000 | VWA2_chr10_114234254_114299489 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 755 | 79 | 35 | 19 | 15 | 2 | 8 | 11 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0002 | 1/1 | 755 | 68 | 13 | 25 | 16 | 3 | 9 | 11 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0003 | 0/0 | 755 | 39 | 21 | 9 | 1 | 4 | 4 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0004 | 0/0 | 755 | 12 | 1 | 1 | 7 | 0 | 3 | 5 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0005 | 0/0 | 755 | 11 | 1 | 3 | 5 | 0 | 2 | 5 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0006 | 0/0 | 755 | 9 | 2 | 2 | 5 | 0 | 0 | 5 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0007 | 0/0 | 755 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0008 | 0/0 | 755 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0009 | 0/0 | 755 | 3 | 0 | 2 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0010 | 0/0 | 755 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0011 | 0/0 | 755 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0012 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0013 | 0/0 | 755 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0014 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0015 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0016 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0017 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0018 | 0/0 | 755 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0019 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0020 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(727): Show |
chr10 | 114234254 | 114299489 |
| a0021 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0022 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0023 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0024 | 0/0 | 755 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| a0025 | 0/0 | 755 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | MPPFL others(750): Show |
chr10 | 114234254 | 114299489 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2265 | 78 | 34 | 19 | 15 | 2 | 8 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0001c0035 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0002c0002 | 1/1 | 2265 | 62 | 9 | 24 | 16 | 3 | 8 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0002c0010 | 0/0 | 2265 | 3 | 3 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0002c0014 | 0/0 | 2265 | 2 | 0 | 1 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0002c0027 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0003c0003 | 0/0 | 2265 | 28 | 11 | 8 | 1 | 4 | 4 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0003c0007 | 0/0 | 2265 | 5 | 5 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0003c0013 | 0/0 | 2265 | 2 | 2 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0003c0016 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0003c0019 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0003c0020 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0003c0023 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0004c0004 | 0/0 | 2265 | 12 | 1 | 1 | 7 | 0 | 3 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0005c0005 | 0/0 | 2265 | 11 | 1 | 3 | 5 | 0 | 2 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0006c0006 | 0/0 | 2265 | 9 | 2 | 2 | 5 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0007c0008 | 0/0 | 2265 | 4 | 4 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0008c0009 | 0/0 | 2265 | 3 | 0 | 2 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0009c0011 | 0/0 | 2265 | 3 | 0 | 2 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0010c0012 | 0/0 | 2265 | 3 | 0 | 0 | 3 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0011c0033 | 0/0 | 2265 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0012c0024 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0013c0028 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0014c0021 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0015c0018 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0016c0034 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0017c0017 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0018c0022 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0019c0015 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0020c0031 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2292): Show |
chr10 | 114234254 | 114299489 | ||
| a0021c0025 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0022c0032 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0023c0026 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0024c0030 | 0/0 | 2265 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 | ||
| a0025c0029 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ATGCC others(2260): Show |
chr10 | 114234254 | 114299489 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5846 | 22 | 0 | 5 | 12 | 0 | 5 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0002 | 0/0 | 5846 | 21 | 4 | 10 | 3 | 2 | 2 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0003 | 0/0 | 5846 | 14 | 14 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0006 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0007 | 0/0 | 5846 | 7 | 7 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0009 | 0/0 | 5846 | 2 | 0 | 1 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0013 | 0/0 | 5846 | 4 | 3 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0016 | 0/0 | 5846 | 2 | 0 | 2 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0022 | 0/0 | 5846 | 2 | 2 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0023 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0030 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0001t0031 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0001c0035t0003 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0002t0001 | 0/0 | 5846 | 35 | 7 | 10 | 13 | 1 | 4 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0002t0002 | 0/0 | 5846 | 10 | 1 | 4 | 2 | 1 | 2 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0002t0003 | 1/0 | 5846 | 4 | 0 | 2 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0002t0006 | 0/0 | 5846 | 6 | 0 | 6 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0002t0009 | 0/0 | 5846 | 4 | 1 | 1 | 1 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0002t0029 | 0/1 | 5846 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0002t0032 | 0/0 | 5846 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0002t0033 | 0/0 | 5846 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0010t0005 | 0/0 | 5846 | 3 | 3 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0014t0003 | 0/0 | 5846 | 2 | 0 | 1 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0002c0027t0005 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0010 | 0/0 | 5846 | 3 | 2 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0011 | 0/0 | 5846 | 5 | 0 | 2 | 0 | 0 | 3 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0012 | 0/0 | 5846 | 2 | 0 | 1 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0017 | 0/0 | 5846 | 3 | 2 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0018 | 0/0 | 5846 | 3 | 2 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0019 | 0/0 | 5846 | 2 | 0 | 1 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0024 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0025 | 0/0 | 5846 | 2 | 1 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0026 | 0/0 | 5846 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0035 | 0/0 | 5846 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0036 | 0/0 | 5846 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0037 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0038 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0039 | 0/0 | 5846 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0003t0040 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0007t0014 | 0/0 | 5846 | 4 | 4 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0007t0024 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0013t0012 | 0/0 | 5846 | 2 | 2 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0016t0003 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0019t0021 | 0/0 | 5846 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0020t0020 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0003c0023t0034 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0004c0004t0001 | 0/0 | 5846 | 2 | 0 | 0 | 1 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0004c0004t0004 | 0/0 | 5846 | 10 | 1 | 1 | 6 | 0 | 2 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0005c0005t0001 | 0/0 | 5846 | 2 | 0 | 0 | 2 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0005c0005t0004 | 0/0 | 5846 | 9 | 1 | 3 | 3 | 0 | 2 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0006c0006t0008 | 0/0 | 5846 | 6 | 0 | 1 | 5 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0006c0006t0015 | 0/0 | 5846 | 3 | 2 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0007c0008t0005 | 0/0 | 5846 | 4 | 4 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0008c0009t0010 | 0/0 | 5846 | 3 | 0 | 2 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0009c0011t0001 | 0/0 | 5846 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0009c0011t0002 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0009c0011t0006 | 0/0 | 5846 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0010c0012t0001 | 0/0 | 5846 | 2 | 0 | 0 | 2 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0010c0012t0004 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0011c0033t0003 | 0/0 | 5846 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0012c0024t0003 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0013c0028t0016 | 0/0 | 5846 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0014c0021t0020 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0015c0018t0021 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0016c0034t0005 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0017c0017t0027 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0018c0022t0015 | 0/0 | 5846 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0019c0015t0028 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0020c0031t0001 | 0/0 | 5878 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5873): Show |
chr10 | 114234254 | 114299489 |
| a0021c0025t0004 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0022c0032t0001 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0023c0026t0004 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0024c0030t0004 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| a0025c0029t0023 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | ACAGT others(5841): Show |
chr10 | 114234254 | 114299489 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0009g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0013g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0013g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0013g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0016g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0016g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0022g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0022g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0023g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0030g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0001t0031g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0001c0035t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0003g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0009g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0009g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0029g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0032g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0002t0033g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0010t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0010t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0010t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0014t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0014t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0002c0027t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0010g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0011g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0011g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0011g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0011g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0011g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0012g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0012g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0017g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0017g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0017g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0018g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0018g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0018g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0019g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0019g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0024g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0025g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0025g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0026g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0035g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0036g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0037g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0038g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0039g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0003t0040g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0007t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0007t0014g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0007t0014g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0007t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0007t0024g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0013t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0013t0012g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0016t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0019t0021g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0020t0020g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0003c0023t0034g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0004c0004t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0005c0005t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0006c0006t0008g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0006c0006t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0006c0006t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0006c0006t0008g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0006c0006t0008g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0006c0006t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0006c0006t0015g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0006c0006t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0006c0006t0015g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0007c0008t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0007c0008t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0007c0008t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0007c0008t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0008c0009t0010g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0008c0009t0010g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0008c0009t0010g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0009c0011t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0009c0011t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0009c0011t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0010c0012t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0010c0012t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0010c0012t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0011c0033t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0012c0024t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0013c0028t0016g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0014c0021t0020g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0015c0018t0021g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0016c0034t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0017c0017t0027g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0018c0022t0015g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0019c0015t0028g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0020c0031t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0021c0025t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0022c0032t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0023c0026t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0024c0030t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| a0025c0029t0023g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0232 | EUR | GBR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0207 | EUR | GBR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00280 | hp1 | a0008 | c0009 | t0010 | g0056 | EUR | FIN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00280 | hp2 | a0002 | c0002 | t0003 | g0129 | EUR | FIN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00323 | hp1 | a0003 | c0003 | t0018 | g0023 | EUR | FIN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0164 | EUR | FIN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00438 | hp1 | a0009 | c0011 | t0002 | g0080 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00438 | hp2 | a0004 | c0004 | t0004 | g0238 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00609 | hp2 | a0004 | c0004 | t0001 | g0124 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00642 | hp1 | a0004 | c0004 | t0004 | g0147 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00642 | hp2 | a0003 | c0003 | t0011 | g0017 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00673 | hp2 | a0010 | c0012 | t0001 | g0120 | EAS | CHS | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00735 | hp1 | a0011 | c0033 | t0003 | g0197 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00735 | hp2 | a0001 | c0001 | t0016 | g0195 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00738 | hp1 | a0006 | c0006 | t0015 | g0053 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00741 | hp1 | a0002 | c0002 | t0006 | g0082 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01071 | hp1 | a0002 | c0014 | t0003 | g0205 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01074 | hp2 | a0003 | c0003 | t0012 | g0025 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01081 | hp2 | a0002 | c0002 | t0003 | g0109 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01099 | hp1 | a0002 | c0002 | t0006 | g0112 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01099 | hp2 | a0003 | c0003 | t0025 | g0011 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01106 | hp2 | a0006 | c0006 | t0008 | g0037 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01109 | hp1 | a0003 | c0003 | t0017 | g0059 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01109 | hp2 | a0001 | c0001 | t0013 | g0236 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01169 | hp1 | a0005 | c0005 | t0004 | g0116 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01169 | hp2 | a0005 | c0005 | t0004 | g0136 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01175 | hp1 | a0003 | c0003 | t0019 | g0028 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0071 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01243 | hp2 | a0003 | c0003 | t0011 | g0018 | AMR | PUR | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01256 | hp1 | a0003 | c0003 | t0035 | g0016 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0067 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01258 | hp2 | a0003 | c0003 | t0036 | g0022 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01346 | hp2 | a0008 | c0009 | t0010 | g0058 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01358 | hp2 | a0002 | c0002 | t0009 | g0229 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01361 | hp1 | a0003 | c0019 | t0021 | g0024 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01361 | hp2 | a0009 | c0011 | t0006 | g0081 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01884 | hp1 | a0001 | c0001 | t0022 | g0158 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0110 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01928 | hp1 | a0002 | c0002 | t0006 | g0092 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01934 | hp2 | a0002 | c0002 | t0006 | g0093 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01952 | hp1 | a0002 | c0002 | t0033 | g0220 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0221 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01975 | hp2 | a0002 | c0002 | t0006 | g0097 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01981 | hp1 | a0009 | c0011 | t0001 | g0083 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02055 | hp1 | a0003 | c0016 | t0003 | g0060 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | KHV | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02135 | hp1 | a0003 | c0003 | t0019 | g0032 | EAS | KHV | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02135 | hp2 | a0002 | c0002 | t0009 | g0202 | EAS | KHV | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02145 | hp2 | a0001 | c0035 | t0003 | g0046 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02148 | hp2 | a0002 | c0002 | t0006 | g0115 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0173 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0074 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02258 | hp2 | a0003 | c0007 | t0014 | g0009 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02273 | hp1 | a0005 | c0005 | t0004 | g0212 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02280 | hp1 | a0001 | c0001 | t0022 | g0099 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02280 | hp2 | a0003 | c0007 | t0014 | g0008 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02451 | hp2 | a0003 | c0003 | t0018 | g0234 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02572 | hp1 | a0003 | c0003 | t0038 | g0048 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0086 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02602 | hp1 | a0002 | c0014 | t0003 | g0206 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02622 | hp1 | a0006 | c0006 | t0015 | g0052 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02630 | hp2 | a0003 | c0003 | t0010 | g0047 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02647 | hp1 | a0001 | c0001 | t0030 | g0159 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02647 | hp2 | a0003 | c0013 | t0012 | g0157 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02698 | hp1 | a0003 | c0003 | t0011 | g0020 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02717 | hp2 | a0004 | c0004 | t0004 | g0245 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02738 | hp1 | a0001 | c0001 | t0009 | g0243 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0095 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02809 | hp1 | a0003 | c0003 | t0017 | g0014 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02886 | hp1 | a0001 | c0001 | t0023 | g0165 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02922 | hp2 | a0003 | c0003 | t0037 | g0010 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02970 | hp2 | a0005 | c0005 | t0004 | g0196 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02976 | hp1 | a0007 | c0008 | t0005 | g0130 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02976 | hp2 | a0003 | c0020 | t0020 | g0039 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03017 | hp1 | a0013 | c0028 | t0016 | g0108 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03041 | hp1 | a0003 | c0013 | t0012 | g0041 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03041 | hp2 | a0003 | c0003 | t0024 | g0003 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03098 | hp1 | a0014 | c0021 | t0020 | g0233 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03130 | hp1 | a0003 | c0003 | t0025 | g0051 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0105 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03139 | hp1 | a0015 | c0018 | t0021 | g0043 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03139 | hp2 | a0003 | c0003 | t0018 | g0235 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03209 | hp2 | a0016 | c0034 | t0005 | g0088 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0189 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03225 | hp2 | a0003 | c0007 | t0014 | g0007 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03239 | hp2 | a0002 | c0002 | t0032 | g0208 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0100 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03453 | hp2 | a0003 | c0003 | t0010 | g0050 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0192 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03492 | hp1 | a0005 | c0005 | t0004 | g0091 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03516 | hp1 | a0002 | c0010 | t0005 | g0113 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03516 | hp2 | a0001 | c0001 | t0031 | g0144 | AFR | ESN | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0140 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03540 | hp2 | a0003 | c0007 | t0024 | g0004 | AFR | GWD | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03579 | hp1 | a0017 | c0017 | t0027 | g0040 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03579 | hp2 | a0007 | c0008 | t0005 | g0131 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03688 | hp1 | a0002 | c0002 | t0009 | g0122 | SAS | STU | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03704 | hp1 | a0003 | c0003 | t0011 | g0021 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03704 | hp2 | a0018 | c0022 | t0015 | g0054 | SAS | PJL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03834 | hp1 | a0003 | c0003 | t0011 | g0015 | SAS | BEB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0214 | SAS | BEB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0141 | SAS | BEB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0076 | SAS | BEB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG04184 | hp1 | a0004 | c0004 | t0004 | g0151 | SAS | BEB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG04184 | hp2 | a0003 | c0003 | t0026 | g0027 | SAS | BEB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG04199 | hp1 | a0005 | c0005 | t0004 | g0231 | SAS | STU | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG04199 | hp2 | a0004 | c0004 | t0001 | g0175 | SAS | STU | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18522 | hp1 | a0003 | c0023 | t0034 | g0005 | AFR | YRI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18522 | hp2 | a0007 | c0008 | t0005 | g0132 | AFR | YRI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | YRI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18906 | hp2 | a0019 | c0015 | t0028 | g0042 | AFR | YRI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18939 | hp2 | a0005 | c0005 | t0004 | g0203 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18945 | hp2 | a0006 | c0006 | t0008 | g0034 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18947 | hp1 | a0005 | c0005 | t0004 | g0225 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18954 | hp1 | a0010 | c0012 | t0001 | g0077 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18960 | hp2 | a0004 | c0004 | t0004 | g0128 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18970 | hp2 | a0006 | c0006 | t0008 | g0038 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18977 | hp2 | a0020 | c0031 | t0001 | g0146 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18990 | hp1 | a0004 | c0004 | t0004 | g0127 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18990 | hp2 | a0005 | c0005 | t0001 | g0226 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18994 | hp2 | a0021 | c0025 | t0004 | g0209 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18999 | hp1 | a0022 | c0032 | t0001 | g0064 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA18999 | hp2 | a0004 | c0004 | t0004 | g0065 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19000 | hp1 | a0006 | c0006 | t0008 | g0033 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19000 | hp2 | a0023 | c0026 | t0004 | g0237 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19007 | hp2 | a0006 | c0006 | t0008 | g0035 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19010 | hp2 | a0005 | c0005 | t0004 | g0222 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19011 | hp2 | a0010 | c0012 | t0004 | g0079 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0084 | AFR | LWK | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | LWK | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19064 | hp1 | a0004 | c0004 | t0004 | g0188 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19065 | hp1 | a0024 | c0030 | t0004 | g0163 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19067 | hp1 | a0005 | c0005 | t0001 | g0204 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19088 | hp1 | a0004 | c0004 | t0004 | g0125 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19090 | hp1 | a0006 | c0006 | t0008 | g0036 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19240 | hp1 | a0003 | c0003 | t0017 | g0013 | AFR | YRI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0119 | AFR | YRI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20129 | hp1 | a0003 | c0007 | t0014 | g0006 | AFR | ASW | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20129 | hp2 | a0002 | c0002 | t0009 | g0096 | AFR | ASW | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | TSI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20752 | hp2 | a0003 | c0003 | t0039 | g0012 | EUR | TSI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20805 | hp1 | a0003 | c0003 | t0010 | g0019 | EUR | TSI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20805 | hp2 | a0003 | c0003 | t0012 | g0026 | EUR | TSI | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20905 | hp1 | a0004 | c0004 | t0004 | g0244 | SAS | GIH | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | GIH | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01123 | hp1 | a0008 | c0009 | t0010 | g0055 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG01123 | hp2 | a0001 | c0001 | t0016 | g0103 | AMR | CLM | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0139 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02486 | hp1 | a0003 | c0003 | t0040 | g0057 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02559 | hp1 | a0012 | c0024 | t0003 | g0090 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG02559 | hp2 | a0002 | c0010 | t0005 | g0111 | AFR | ACB | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03471 | hp1 | a0006 | c0006 | t0015 | g0049 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG03471 | hp2 | a0002 | c0010 | t0005 | g0073 | AFR | MSL | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG06807 | hp1 | a0007 | c0008 | t0005 | g0089 | AFR | USA | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0142 | AFR | USA | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0075 | AFR | USA | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | USA | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA21309 | hp1 | a0025 | c0029 | t0023 | g0194 | AFR | LWK | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| NA21309 | hp2 | a0002 | c0027 | t0005 | g0135 | AFR | LWK | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0029 | g0143 | REF | REF | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0003 | g0138 | REF | REF | VWA2_chr10_114234254_114299489 | VWA2 | chr10 | 114234254 | 114299489 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:114248705 | T | A | 6 | a0003 a0006 a0014 others(3): Show |
26 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(23): Show |
splice_region_variant | LOW | c.-9T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/14 | chr10 | 114248705 | |||||||
| chr10:114248738 | G | A | 8 | a0003 a0006 a0008 others(5): Show |
56 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(53): Show |
missense_variant | MODERATE | c.25G>A | p.Ala9Thr | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/14 | 351/5846 | 25/2268 | 9/755 | chr10 | 114248738 | |||
| chr10:114255010 | A | T | 2 | a0009 a0010 |
6 | HG00438.hp1 HG00673.hp2 HG01361.hp2 others(3): Show |
missense_variant | MODERATE | c.223A>T | p.Ile75Phe | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/14 | 549/5846 | 223/2268 | 75/755 | chr10 | 114255010 | |||
| chr10:114261211 | G | A | 1 | a0019 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.287G>A | p.Ser96Asn | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/14 | 613/5846 | 287/2268 | 96/755 | chr10 | 114261211 | |||
| chr10:114272760 | A | G | 15 | a0001 a0003 a0004 others(12): Show |
150 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(147): Show |
missense_variant | MODERATE | c.392A>G | p.Glu131Gly | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/14 | 718/5846 | 392/2268 | 131/755 | chr10 | 114272760 | |||
| chr10:114286187 | C | T | 1 | a0011 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.1246C>T | p.Arg416Cys | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/14 | 1572/5846 | 1246/2268 | 416/755 | chr10 | 114286187 | |||
| chr10:114286353 | G | A | 1 | a0013 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1412G>A | p.Arg471Gln | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/14 | 1738/5846 | 1412/2268 | 471/755 | chr10 | 114286353 | |||
| chr10:114286388 | G | A | 1 | a0025 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1447G>A | p.Val483Met | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/14 | 1773/5846 | 1447/2268 | 483/755 | chr10 | 114286388 | |||
| chr10:114286427 | C | T | 3 | a0007 a0014 a0016 |
6 | HG02976.hp1 HG03098.hp1 HG03209.hp2 others(3): Show |
missense_variant | MODERATE | c.1486C>T | p.His496Tyr | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/14 | 1812/5846 | 1486/2268 | 496/755 | chr10 | 114286427 | |||
| chr10:114286443 | C | T | 1 | a0023 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.1502C>T | p.Ser501Leu | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/14 | 1828/5846 | 1502/2268 | 501/755 | chr10 | 114286443 | |||
| chr10:114289117 | G | C | 1 | a0017 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1750G>C | p.Gly584Arg | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/14 | 2076/5846 | 1750/2268 | 584/755 | chr10 | 114289117 | |||
| chr10:114289138 | C | T | 1 | a0022 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.1771C>T | p.Arg591Trp | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/14 | 2097/5846 | 1771/2268 | 591/755 | chr10 | 114289138 | |||
| chr10:114289291 | G | A | 2 | a0012 a0015 |
2 | HG02559.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.1924G>A | p.Gly642Arg | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/14 | 2250/5846 | 1924/2268 | 642/755 | chr10 | 114289291 | |||
| chr10:114289434 | A | AGCTTACG others(25): Show |
1 | a0020 | 1 | NA18977.hp2 | frameshift_variant | HIGH | c.2071_2102dupTACGCC others(26): Show |
p.Ile702fs | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/14 | 2429/5846 | 2103/2268 | 701/755 | INFO_REALIGN_3_PRIME | chr10 | 114289434 | ||
| chr10:114290249 | A | G | 9 | a0004 a0005 a0006 others(6): Show |
40 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(37): Show |
missense_variant | MODERATE | c.2132A>G | p.Gln711Arg | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 13/14 | 2458/5846 | 2132/2268 | 711/755 | chr10 | 114290249 | |||
| chr10:114290321 | G | A | 2 | a0021 a0024 |
2 | NA18994.hp2 NA19065.hp1 |
missense_variant | MODERATE | c.2204G>A | p.Arg735His | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 13/14 | 2530/5846 | 2204/2268 | 735/755 | chr10 | 114290321 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:114253700 | C | T | 2 | a0003c0007 a0003c0023 |
6 | HG02258.hp2 HG02280.hp2 HG03225.hp2 others(3): Show |
synonymous_variant | LOW | c.102C>T | p.Ile34Ile | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/14 | 428/5846 | 102/2268 | 34/755 | chr10 | 114253700 | |||
| chr10:114261215 | C | G | 2 | a0008c0009 a0018c0022 |
4 | HG00280.hp1 HG01123.hp1 HG01346.hp2 others(1): Show |
synonymous_variant | LOW | c.291C>G | p.Ser97Ser | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/14 | 617/5846 | 291/2268 | 97/755 | chr10 | 114261215 | |||
| chr10:114272812 | T | C | 1 | a0003c0016 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.444T>C | p.Ala148Ala | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/14 | 770/5846 | 444/2268 | 148/755 | chr10 | 114272812 | |||
| chr10:114277941 | C | T | 1 | a0001c0035 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.594C>T | p.Ser198Ser | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 7/14 | 920/5846 | 594/2268 | 198/755 | chr10 | 114277941 | |||
| chr10:114278759 | G | A | 2 | a0003c0007 a0003c0023 |
6 | HG02258.hp2 HG02280.hp2 HG03225.hp2 others(3): Show |
synonymous_variant | LOW | c.741G>A | p.Leu247Leu | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/14 | 1067/5846 | 741/2268 | 247/755 | chr10 | 114278759 | |||
| chr10:114284966 | C | T | 7 | a0002c0010 a0002c0027 a0003c0020 others(4): Show |
12 | HG02559.hp2 HG02976.hp1 HG02976.hp2 others(9): Show |
synonymous_variant | LOW | c.993C>T | p.Asn331Asn | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/14 | 1319/5846 | 993/2268 | 331/755 | chr10 | 114284966 | |||
| chr10:114285997 | G | A | 7 | a0002c0010 a0002c0027 a0003c0020 others(4): Show |
12 | HG02559.hp2 HG02976.hp1 HG02976.hp2 others(9): Show |
synonymous_variant | LOW | c.1056G>A | p.Ala352Ala | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/14 | 1382/5846 | 1056/2268 | 352/755 | chr10 | 114285997 | |||
| chr10:114286036 | C | T | 2 | a0002c0014 a0003c0019 |
3 | HG01071.hp1 HG01361.hp1 HG02602.hp1 |
synonymous_variant | LOW | c.1095C>T | p.Phe365Phe | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/14 | 1421/5846 | 1095/2268 | 365/755 | chr10 | 114286036 | |||
| chr10:114288960 | C | T | 1 | a0002c0027 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1593C>T | p.Asp531Asp | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/14 | 1919/5846 | 1593/2268 | 531/755 | chr10 | 114288960 | |||
| chr10:114289377 | C | T | 1 | a0003c0013 | 2 | HG02647.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.2010C>T | p.Val670Val | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/14 | 2336/5846 | 2010/2268 | 670/755 | chr10 | 114289377 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:114239333 | C | T | 18 | a0003c0003t0010 a0003c0003t0011 a0003c0003t0017 others(15): Show |
36 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(33): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-247C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/14 | chr10 | 114239333 | |||||||
| chr10:114239548 | G | A | 18 | a0003c0003t0010 a0003c0003t0011 a0003c0003t0017 others(15): Show |
36 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-32G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/14 | 9166 | chr10 | 114239548 | ||||||
| chr10:114239560 | T | G | 18 | a0003c0003t0010 a0003c0003t0011 a0003c0003t0017 others(15): Show |
36 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-20T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/14 | 9154 | chr10 | 114239560 | ||||||
| chr10:114291258 | G | A | 4 | a0001c0001t0016 a0003c0003t0035 a0003c0003t0036 others(1): Show |
5 | HG00735.hp2 HG01123.hp2 HG01256.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*21G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 21 | chr10 | 114291258 | ||||||
| chr10:114291370 | C | T | 2 | a0001c0001t0023 a0025c0029t0023 |
2 | HG02886.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*133C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 133 | chr10 | 114291370 | ||||||
| chr10:114291572 | G | T | 1 | a0002c0002t0033 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*335G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 335 | chr10 | 114291572 | ||||||
| chr10:114291619 | A | T | 3 | a0001c0001t0006 a0002c0002t0006 a0009c0011t0006 |
8 | HG00741.hp1 HG01099.hp1 HG01361.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*382A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 382 | chr10 | 114291619 | ||||||
| chr10:114291757 | G | T | 2 | a0001c0001t0022 a0019c0015t0028 |
3 | HG01884.hp1 HG02280.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*520G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 520 | chr10 | 114291757 | ||||||
| chr10:114291809 | G | A | 11 | a0001c0001t0002 a0001c0001t0022 a0001c0001t0030 others(8): Show |
44 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*572G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 572 | chr10 | 114291809 | ||||||
| chr10:114291865 | A | G | 1 | a0001c0001t0030 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*628A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 628 | chr10 | 114291865 | ||||||
| chr10:114292003 | G | A | 6 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0031 others(3): Show |
20 | HG00323.hp1 HG01109.hp2 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*766G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 766 | chr10 | 114292003 | ||||||
| chr10:114292079 | C | A | 1 | a0017c0017t0027 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 842 | chr10 | 114292079 | ||||||
| chr10:114292208 | C | T | 1 | a0003c0003t0040 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*971C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 971 | chr10 | 114292208 | ||||||
| chr10:114292309 | A | G | 1 | a0017c0017t0027 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1072A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 1072 | chr10 | 114292309 | ||||||
| chr10:114292439 | C | T | 3 | a0001c0001t0007 a0003c0003t0038 a0003c0007t0014 |
12 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1202C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 1202 | chr10 | 114292439 | ||||||
| chr10:114292492 | G | A | 4 | a0001c0001t0009 a0002c0002t0009 a0003c0003t0035 others(1): Show |
8 | HG01256.hp1 HG01256.hp2 HG01358.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1255G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 1255 | chr10 | 114292492 | ||||||
| chr10:114292556 | G | A | 7 | a0002c0010t0005 a0002c0027t0005 a0003c0020t0020 others(4): Show |
12 | HG02559.hp2 HG02976.hp1 HG02976.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1319G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 1319 | chr10 | 114292556 | ||||||
| chr10:114292603 | G | A | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(33): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1366G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 1366 | chr10 | 114292603 | ||||||
| chr10:114292708 | G | A | 9 | a0004c0004t0004 a0005c0005t0004 a0006c0006t0008 others(6): Show |
33 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1471G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 1471 | chr10 | 114292708 | ||||||
| chr10:114292983 | A | G | 4 | a0001c0001t0013 a0002c0002t0032 a0003c0003t0011 others(1): Show |
13 | HG00323.hp1 HG00642.hp2 HG01109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1746A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 1746 | chr10 | 114292983 | ||||||
| chr10:114293177 | A | C | 1 | a0003c0003t0037 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1940A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 1940 | chr10 | 114293177 | ||||||
| chr10:114293241 | C | T | 9 | a0004c0004t0004 a0005c0005t0004 a0006c0006t0008 others(6): Show |
33 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2004C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 2004 | chr10 | 114293241 | ||||||
| chr10:114293242 | G | A | 1 | a0002c0002t0033 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2005G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 2005 | chr10 | 114293242 | ||||||
| chr10:114293509 | A | G | 1 | a0003c0003t0026 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2272A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 2272 | chr10 | 114293509 | ||||||
| chr10:114293930 | A | T | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(46): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*2693A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 2693 | chr10 | 114293930 | ||||||
| chr10:114294385 | A | G | 1 | a0001c0001t0031 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3148A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 14/14 | 3148 | chr10 | 114294385 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:114239610 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11+41C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114239610 | |||||||
| chr10:114239811 | T | C | 1 | a0002c0002t0001g0001 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-11+242T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114239811 | |||||||
| chr10:114239821 | C | T | 1 | a0004c0004t0004g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-11+252C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114239821 | |||||||
| chr10:114239881 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11+312T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114239881 | |||||||
| chr10:114240231 | A | C | 8 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(5): Show |
8 | HG00438.hp2 HG00673.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+662A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114240231 | |||||||
| chr10:114240294 | C | T | 1 | a0001c0001t0013g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+725C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114240294 | |||||||
| chr10:114240339 | C | G | 2 | a0003c0003t0018g0234 a0003c0003t0018g0235 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-11+770C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114240339 | |||||||
| chr10:114240413 | G | T | 1 | a0014c0021t0020g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-11+844G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114240413 | |||||||
| chr10:114240694 | C | T | 35 | a0001c0001t0001g0230 a0001c0001t0002g0232 a0002c0002t0001g0198 others(32): Show |
35 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.-11+1125C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114240694 | |||||||
| chr10:114240724 | T | C | 23 | a0003c0003t0010g0019 a0003c0003t0011g0015 a0003c0003t0011g0017 others(20): Show |
23 | HG00323.hp1 HG00642.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.-11+1155T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114240724 | |||||||
| chr10:114240910 | G | C | 21 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(18): Show |
21 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-11+1341G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114240910 | |||||||
| chr10:114241204 | G | A | 2 | a0001c0001t0002g0045 a0001c0001t0006g0044 |
2 | HG01433.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-11+1635G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114241204 | |||||||
| chr10:114241568 | G | A | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-11+1999G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114241568 | |||||||
| chr10:114241658 | G | A | 1 | a0002c0002t0001g0198 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-11+2089G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114241658 | |||||||
| chr10:114241725 | G | A | 59 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(56): Show |
59 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11+2156G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114241725 | |||||||
| chr10:114241758 | C | T | 16 | a0003c0003t0010g0019 a0003c0003t0011g0015 a0003c0003t0011g0017 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11+2189C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114241758 | |||||||
| chr10:114242037 | A | C | 117 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(114): Show |
117 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+2468A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114242037 | |||||||
| chr10:114242211 | C | A | 1 | a0003c0003t0010g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-11+2642C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114242211 | |||||||
| chr10:114242317 | G | A | 35 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(32): Show |
35 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-11+2748G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114242317 | |||||||
| chr10:114242363 | A | G | 59 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(56): Show |
59 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11+2794A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114242363 | |||||||
| chr10:114242436 | A | G | 1 | a0011c0033t0003g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-11+2867A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114242436 | |||||||
| chr10:114242508 | A | G | 35 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(32): Show |
35 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-11+2939A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114242508 | |||||||
| chr10:114242566 | GC | G | 5 | a0003c0013t0012g0041 a0003c0020t0020g0039 a0015c0018t0021g0043 others(2): Show |
5 | HG02976.hp2 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+2998delC | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114242566 | |||||||
| chr10:114242696 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-11+3127C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114242696 | |||||||
| chr10:114242924 | A | G | 6 | a0003c0003t0010g0047 a0003c0003t0040g0057 a0008c0009t0010g0055 others(3): Show |
6 | HG00280.hp1 HG01123.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+3355A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114242924 | |||||||
| chr10:114243273 | T | C | 1 | a0003c0003t0024g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11+3704T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243273 | |||||||
| chr10:114243294 | T | C | 116 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-11+3725T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243294 | |||||||
| chr10:114243489 | G | A | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-11+3920G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243489 | |||||||
| chr10:114243557 | T | C | 1 | a0001c0001t0031g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-11+3988T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243557 | |||||||
| chr10:114243612 | T | C | 2 | a0001c0001t0001g0145 a0020c0031t0001g0146 |
2 | NA18947.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-11+4043T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243612 | |||||||
| chr10:114243613 | T | TA | 35 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(32): Show |
35 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-11+4044_-11+4045i others(3): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243613 | |||||||
| chr10:114243715 | C | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(13): Show |
16 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11+4146C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243715 | |||||||
| chr10:114243728 | G | A | 35 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(32): Show |
35 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-11+4159G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243728 | |||||||
| chr10:114243784 | C | T | 3 | a0002c0002t0001g0001 a0002c0002t0001g0142 a0002c0002t0002g0141 |
3 | HG01496.hp2 HG03927.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-11+4215C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243784 | |||||||
| chr10:114243785 | G | A | 22 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(19): Show |
22 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11+4216G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114243785 | |||||||
| chr10:114244038 | G | A | 1 | a0002c0002t0001g0199 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-11+4469G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244038 | |||||||
| chr10:114244118 | T | C | 59 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(56): Show |
59 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-11+4549T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244118 | |||||||
| chr10:114244160 | T | C | 1 | a0002c0002t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-10-4544T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244160 | |||||||
| chr10:114244438 | C | T | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-4266C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244438 | |||||||
| chr10:114244475 | C | T | 37 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(34): Show |
37 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10-4229C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244475 | |||||||
| chr10:114244574 | C | T | 1 | a0001c0001t0013g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-10-4130C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244574 | |||||||
| chr10:114244633 | T | A | 1 | a0002c0002t0002g0062 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-10-4071T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244633 | |||||||
| chr10:114244633 | T | TA | 116 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-10-4062dupA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114244633 | ||||||
| chr10:114244924 | A | G | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10-3780A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244924 | |||||||
| chr10:114244975 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-3729T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244975 | |||||||
| chr10:114244994 | C | T | 1 | a0004c0004t0004g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-10-3710C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114244994 | |||||||
| chr10:114245121 | G | A | 1 | a0022c0032t0001g0064 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-10-3583G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245121 | |||||||
| chr10:114245209 | G | T | 37 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(34): Show |
37 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10-3495G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245209 | |||||||
| chr10:114245211 | C | T | 1 | a0006c0006t0008g0038 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-10-3493C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245211 | |||||||
| chr10:114245218 | G | A | 35 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(32): Show |
35 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10-3486G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245218 | |||||||
| chr10:114245289 | G | A | 1 | a0003c0003t0010g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10-3415G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245289 | |||||||
| chr10:114245292 | C | T | 1 | a0025c0029t0023g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10-3412C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245292 | |||||||
| chr10:114245305 | A | C | 116 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-10-3399A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245305 | |||||||
| chr10:114245329 | ATGTGGCA others(9): Show |
A | 1 | a0001c0001t0002g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-3371_-10-3356d others(18): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114245329 | ||||||
| chr10:114245542 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10-3162C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245542 | |||||||
| chr10:114245619 | T | C | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-3085T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245619 | |||||||
| chr10:114245709 | C | A | 2 | a0001c0001t0031g0144 a0005c0005t0004g0196 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-10-2995C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245709 | |||||||
| chr10:114245736 | T | G | 59 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(56): Show |
59 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-10-2968T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245736 | |||||||
| chr10:114245776 | T | C | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10-2928T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114245776 | |||||||
| chr10:114246089 | G | A | 1 | a0002c0002t0001g0200 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-10-2615G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246089 | |||||||
| chr10:114246249 | C | T | 2 | a0015c0018t0021g0043 a0019c0015t0028g0042 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-10-2455C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246249 | |||||||
| chr10:114246267 | G | A | 1 | a0003c0003t0010g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10-2437G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246267 | |||||||
| chr10:114246361 | C | T | 22 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(19): Show |
22 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-10-2343C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246361 | |||||||
| chr10:114246362 | G | A | 1 | a0003c0003t0024g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-10-2342G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246362 | |||||||
| chr10:114246488 | T | C | 59 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(56): Show |
59 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-10-2216T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246488 | |||||||
| chr10:114246505 | C | CA | 32 | a0001c0001t0002g0068 a0001c0001t0002g0148 a0001c0001t0003g0066 others(29): Show |
32 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-10-2179dupA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(11): Show |
4 | a0003c0003t0040g0057 a0003c0007t0014g0008 a0003c0016t0003g0060 others(1): Show |
4 | HG01346.hp2 HG02055.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-2196_-10-2179d others(20): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(12): Show |
2 | a0008c0009t0010g0055 a0008c0009t0010g0056 |
2 | HG00280.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-10-2197_-10-2179d others(21): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(14): Show |
1 | a0018c0022t0015g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-10-2179_-10-2178i others(23): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(15): Show |
1 | a0006c0006t0015g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-2179_-10-2178i others(24): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(16): Show |
4 | a0003c0003t0010g0050 a0003c0003t0025g0051 a0003c0007t0014g0007 others(1): Show |
4 | HG03130.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-2179_-10-2178i others(25): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(17): Show |
2 | a0003c0003t0038g0048 a0003c0007t0014g0006 |
2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-10-2179_-10-2178i others(26): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(19): Show |
1 | a0003c0003t0010g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10-2179_-10-2178i others(28): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(21): Show |
1 | a0003c0003t0024g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-10-2179_-10-2178i others(30): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(24): Show |
1 | a0003c0023t0034g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-10-2179_-10-2178i others(33): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | C | CAAAAAAA others(36): Show |
1 | a0003c0007t0024g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-10-2179_-10-2178i others(45): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | CAAA | C | 5 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(2): Show |
5 | HG01074.hp2 HG01175.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-2181_-10-2179d others(5): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246505 | CAAAA | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(11): Show |
14 | HG01106.hp2 HG01928.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10-2182_-10-2179d others(6): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114246505 | ||||||
| chr10:114246525 | AC | A | 10 | a0003c0003t0010g0019 a0003c0003t0011g0015 a0003c0003t0011g0017 others(7): Show |
10 | HG00323.hp1 HG00642.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-2178delC | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246525 | |||||||
| chr10:114246526 | C | A | 27 | a0003c0003t0010g0047 a0003c0003t0010g0050 a0003c0003t0017g0013 others(24): Show |
27 | HG00280.hp1 HG00738.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-10-2178C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246526 | |||||||
| chr10:114246635 | T | A | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-2069T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246635 | |||||||
| chr10:114246677 | T | C | 59 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(56): Show |
59 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-10-2027T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246677 | |||||||
| chr10:114246747 | C | T | 2 | a0015c0018t0021g0043 a0019c0015t0028g0042 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-10-1957C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246747 | |||||||
| chr10:114246763 | C | G | 36 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(33): Show |
36 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-10-1941C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246763 | |||||||
| chr10:114246801 | G | A | 7 | a0003c0003t0024g0003 a0003c0007t0014g0006 a0003c0007t0014g0007 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-1903G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246801 | |||||||
| chr10:114246968 | A | G | 1 | a0003c0003t0018g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-10-1736A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246968 | |||||||
| chr10:114246971 | G | T | 36 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(33): Show |
36 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-10-1733G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246971 | |||||||
| chr10:114246977 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10-1727C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246977 | |||||||
| chr10:114246984 | T | C | 59 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0029 others(56): Show |
59 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-10-1720T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114246984 | |||||||
| chr10:114247131 | T | C | 1 | a0005c0005t0004g0203 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-10-1573T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114247131 | |||||||
| chr10:114247189 | G | GA | 6 | a0003c0003t0017g0059 a0004c0004t0004g0065 a0004c0004t0004g0147 others(3): Show |
6 | HG00438.hp2 HG00642.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-1501dupA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114247189 | ||||||
| chr10:114247189 | GA | G | 34 | a0003c0003t0010g0019 a0003c0003t0011g0015 a0003c0003t0011g0017 others(31): Show |
34 | HG00323.hp1 HG00642.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10-1501delA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114247189 | ||||||
| chr10:114247372 | C | T | 26 | a0001c0035t0003g0046 a0003c0003t0012g0025 a0003c0003t0012g0026 others(23): Show |
26 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-10-1332C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114247372 | |||||||
| chr10:114247400 | T | C | 238 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-10-1304T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114247400 | |||||||
| chr10:114247590 | C | T | 4 | a0001c0001t0001g0230 a0002c0002t0009g0202 a0002c0002t0009g0229 others(1): Show |
4 | HG01358.hp2 HG02135.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-1114C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114247590 | |||||||
| chr10:114247663 | C | CA | 16 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(13): Show |
16 | HG00438.hp2 HG00642.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-1030dupA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114247663 | ||||||
| chr10:114247685 | C | T | 1 | a0001c0001t0003g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10-1019C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114247685 | |||||||
| chr10:114247825 | A | G | 1 | a0003c0003t0017g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-10-879A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114247825 | |||||||
| chr10:114247845 | G | A | 6 | a0003c0003t0010g0047 a0003c0003t0040g0057 a0008c0009t0010g0055 others(3): Show |
6 | HG00280.hp1 HG01123.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-859G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114247845 | |||||||
| chr10:114248033 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-10-671G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114248033 | |||||||
| chr10:114248107 | C | CA | 39 | a0001c0001t0002g0063 a0001c0001t0002g0148 a0001c0035t0003g0046 others(36): Show |
39 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.-10-581dupA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114248107 | ||||||
| chr10:114248107 | CA | C | 8 | a0001c0001t0002g0191 a0001c0001t0003g0152 a0001c0001t0003g0190 others(5): Show |
8 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-581delA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 114248107 | ||||||
| chr10:114248465 | G | A | 1 | a0003c0003t0010g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10-239G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114248465 | |||||||
| chr10:114248491 | A | C | 59 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.-10-213A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114248491 | |||||||
| chr10:114248540 | C | T | 58 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(55): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-10-164C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114248540 | |||||||
| chr10:114248549 | G | A | 8 | a0001c0001t0001g0145 a0001c0001t0001g0153 a0001c0001t0002g0045 others(5): Show |
8 | HG00597.hp1 HG01433.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-155G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114248549 | |||||||
| chr10:114248572 | T | C | 13 | a0003c0003t0010g0047 a0003c0003t0010g0050 a0003c0003t0017g0059 others(10): Show |
13 | HG00280.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10-132T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114248572 | |||||||
| chr10:114248626 | A | G | 1 | a0025c0029t0023g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10-78A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 1/13 | chr10 | 114248626 | |||||||
| chr10:114249126 | G | A | 1 | a0003c0003t0010g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.52+361G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249126 | |||||||
| chr10:114249129 | T | C | 29 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(26): Show |
29 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.52+364T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249129 | |||||||
| chr10:114249169 | C | T | 1 | a0004c0004t0004g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.52+404C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249169 | |||||||
| chr10:114249468 | C | A | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52+703C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249468 | |||||||
| chr10:114249548 | G | A | 6 | a0003c0003t0010g0047 a0003c0003t0040g0057 a0008c0009t0010g0055 others(3): Show |
6 | HG00280.hp1 HG01123.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+783G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249548 | |||||||
| chr10:114249619 | TGAG | T | 6 | a0003c0003t0017g0014 a0003c0003t0018g0234 a0003c0003t0018g0235 others(3): Show |
6 | HG01099.hp2 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+858_52+860delGA others(1): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114249619 | ||||||
| chr10:114249742 | A | G | 1 | a0008c0009t0010g0058 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.52+977A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249742 | |||||||
| chr10:114249754 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.52+989G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249754 | |||||||
| chr10:114249790 | G | A | 3 | a0002c0002t0001g0207 a0002c0014t0003g0205 a0002c0014t0003g0206 |
3 | HG00099.hp2 HG01071.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.52+1025G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249790 | |||||||
| chr10:114249879 | A | G | 3 | a0001c0001t0022g0158 a0001c0001t0030g0159 a0001c0001t0031g0144 |
3 | HG01884.hp1 HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.52+1114A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249879 | |||||||
| chr10:114249884 | G | A | 1 | a0005c0005t0004g0196 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.52+1119G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114249884 | |||||||
| chr10:114250398 | A | T | 1 | a0002c0002t0001g0228 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.52+1633A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114250398 | |||||||
| chr10:114250458 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.52+1693C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114250458 | |||||||
| chr10:114250487 | CCTTCTGT others(57): Show |
C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.52+1725_52+1788del others(64): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114250487 | ||||||
| chr10:114250766 | G | A | 12 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(9): Show |
12 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+2001G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114250766 | |||||||
| chr10:114250831 | G | C | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.52+2066G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114250831 | |||||||
| chr10:114250870 | G | A | 13 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(10): Show |
13 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+2105G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114250870 | |||||||
| chr10:114251043 | G | A | 2 | a0002c0002t0001g0094 a0002c0002t0002g0095 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.52+2278G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114251043 | |||||||
| chr10:114251073 | C | T | 5 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(2): Show |
5 | HG01074.hp2 HG01175.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+2308C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114251073 | |||||||
| chr10:114251166 | A | G | 5 | a0003c0003t0040g0057 a0008c0009t0010g0055 a0008c0009t0010g0056 others(2): Show |
5 | HG00280.hp1 HG01123.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+2401A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114251166 | |||||||
| chr10:114251660 | C | T | 1 | a0025c0029t0023g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.53-1991C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114251660 | |||||||
| chr10:114251742 | G | A | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.53-1909G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114251742 | |||||||
| chr10:114251820 | A | AT | 69 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(66): Show |
69 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.53-1810dupT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114251820 | ||||||
| chr10:114251820 | A | ATT | 19 | a0001c0001t0001g0186 a0001c0001t0003g0185 a0001c0001t0003g0187 others(16): Show |
19 | HG01175.hp1 HG01358.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.53-1811_53-1810dup others(2): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114251820 | ||||||
| chr10:114251820 | AT | A | 12 | a0001c0001t0022g0158 a0002c0002t0001g0001 a0002c0002t0001g0094 others(9): Show |
12 | HG01074.hp2 HG01256.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-1810delT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114251820 | ||||||
| chr10:114252087 | TGAGCCAC others(3): Show |
T | 1 | a0020c0031t0001g0146 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.53-1562_53-1553del others(10): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114252087 | ||||||
| chr10:114252153 | TTTTTAAA others(10): Show |
T | 1 | a0005c0005t0004g0225 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.53-1493_53-1477del others(17): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114252153 | ||||||
| chr10:114252463 | G | A | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.53-1188G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114252463 | |||||||
| chr10:114252530 | T | TC | 5 | a0001c0001t0002g0063 a0001c0001t0003g0187 a0001c0001t0007g0086 others(2): Show |
5 | HG02572.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-1116dupC | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114252530 | ||||||
| chr10:114252556 | C | G | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-1095C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114252556 | |||||||
| chr10:114252691 | C | T | 1 | a0003c0003t0019g0032 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.53-960C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114252691 | |||||||
| chr10:114252756 | A | AC | 4 | a0001c0001t0003g0187 a0001c0001t0007g0086 a0003c0013t0012g0157 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-892dupC | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114252756 | ||||||
| chr10:114252849 | T | C | 1 | a0005c0005t0001g0204 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.53-802T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114252849 | |||||||
| chr10:114253030 | C | T | 2 | a0003c0003t0035g0016 a0003c0003t0036g0022 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.53-621C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253030 | |||||||
| chr10:114253068 | T | G | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-583T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253068 | |||||||
| chr10:114253073 | T | G | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-578T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253073 | |||||||
| chr10:114253097 | T | C | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.53-554T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253097 | |||||||
| chr10:114253098 | C | A | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-553C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253098 | |||||||
| chr10:114253100 | C | CTTATTGT others(10): Show |
1 | a0001c0001t0001g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.53-550_53-534dupTT others(15): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253100 | ||||||
| chr10:114253117 | T | G | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-534T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253117 | |||||||
| chr10:114253148 | C | A | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-503C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253148 | |||||||
| chr10:114253157 | G | GGGGCTGG others(543): Show |
1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-494_53-493insGG others(548): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253157 | |||||||
| chr10:114253161 | T | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-490T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253161 | |||||||
| chr10:114253162 | A | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-489A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253162 | |||||||
| chr10:114253163 | T | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-488T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253163 | |||||||
| chr10:114253168 | A | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-483A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253168 | |||||||
| chr10:114253175 | A | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-476A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253175 | |||||||
| chr10:114253176 | A | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-475A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253176 | |||||||
| chr10:114253184 | T | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-467T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253184 | |||||||
| chr10:114253184 | T | G | 1 | a0005c0005t0001g0226 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.53-467T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253184 | |||||||
| chr10:114253184 | T | TCTCCCTC others(455): Show |
1 | a0005c0005t0001g0204 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.53-466_53-465insTC others(460): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253184 | ||||||
| chr10:114253187 | C | T | 1 | a0005c0005t0001g0204 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.53-464C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253187 | |||||||
| chr10:114253193 | C | T | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-458C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253193 | |||||||
| chr10:114253194 | T | C | 1 | a0005c0005t0001g0204 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.53-457T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253194 | |||||||
| chr10:114253196 | T | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-455T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253196 | |||||||
| chr10:114253196 | T | TCTCCTCT others(530): Show |
1 | a0002c0002t0001g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(535): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253196 | ||||||
| chr10:114253198 | T | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-453T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253198 | |||||||
| chr10:114253198 | T | TCCTCTCC others(482): Show |
1 | a0001c0001t0002g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(487): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(503): Show |
1 | a0001c0001t0002g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(508): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(480): Show |
1 | a0003c0007t0014g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(485): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(451): Show |
5 | a0003c0007t0014g0006 a0003c0007t0014g0007 a0003c0007t0014g0008 others(2): Show |
5 | HG02280.hp2 HG03225.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(456): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(397): Show |
1 | a0006c0006t0008g0033 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(402): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(437): Show |
4 | a0006c0006t0008g0034 a0006c0006t0008g0035 a0006c0006t0008g0036 others(1): Show |
4 | NA18945.hp2 NA18970.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(442): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(479): Show |
1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(484): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(472): Show |
1 | a0003c0003t0011g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(477): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(586): Show |
1 | a0003c0003t0010g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(591): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(507): Show |
1 | a0003c0003t0017g0013 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(512): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(484): Show |
1 | a0003c0003t0010g0019 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(489): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(471): Show |
10 | a0003c0003t0011g0015 a0003c0003t0011g0020 a0003c0003t0011g0021 others(7): Show |
10 | HG00323.hp1 HG01099.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(476): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(447): Show |
2 | a0003c0013t0012g0041 a0017c0017t0027g0040 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(452): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(434): Show |
1 | a0015c0018t0021g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(439): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(434): Show |
1 | a0019c0015t0028g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(439): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(444): Show |
1 | a0003c0003t0019g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(449): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(391): Show |
1 | a0003c0003t0026g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(396): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(442): Show |
2 | a0003c0003t0019g0032 a0006c0006t0008g0037 |
2 | HG01106.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(447): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(461): Show |
1 | a0003c0020t0020g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(466): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(469): Show |
2 | a0003c0003t0012g0025 a0003c0019t0021g0024 |
2 | HG01074.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(474): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(449): Show |
2 | a0008c0009t0010g0055 a0008c0009t0010g0058 |
2 | HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(454): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(463): Show |
2 | a0008c0009t0010g0056 a0018c0022t0015g0054 |
2 | HG00280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(468): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(461): Show |
1 | a0003c0003t0018g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(466): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(473): Show |
1 | a0003c0003t0024g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(478): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(476): Show |
1 | a0003c0003t0018g0235 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(481): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(442): Show |
1 | a0014c0021t0020g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(447): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(463): Show |
1 | a0003c0003t0040g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(468): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(510): Show |
1 | a0024c0030t0004g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(515): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(505): Show |
1 | a0001c0001t0003g0171 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(510): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(663): Show |
1 | a0021c0025t0004g0209 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(668): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(475): Show |
1 | a0007c0008t0005g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(480): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(492): Show |
2 | a0001c0001t0003g0066 a0001c0001t0007g0100 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(497): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(472): Show |
1 | a0001c0001t0001g0239 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(477): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(472): Show |
1 | a0001c0001t0009g0067 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(477): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(526): Show |
1 | a0001c0001t0001g0154 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(531): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(552): Show |
1 | a0002c0002t0001g0101 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(557): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(530): Show |
1 | a0001c0001t0002g0172 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(535): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(514): Show |
1 | a0001c0001t0003g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(519): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(505): Show |
1 | a0001c0001t0003g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(510): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(509): Show |
1 | a0001c0001t0003g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(514): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(508): Show |
2 | a0001c0001t0007g0173 a0001c0001t0007g0189 |
2 | HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(513): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(512): Show |
1 | a0001c0001t0003g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(517): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(497): Show |
1 | a0002c0002t0002g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(502): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(485): Show |
1 | a0004c0004t0004g0245 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(490): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(512): Show |
1 | a0001c0001t0023g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(517): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(520): Show |
1 | a0004c0004t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(525): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(497): Show |
7 | a0001c0001t0001g0166 a0001c0001t0001g0177 a0001c0001t0001g0186 others(4): Show |
7 | HG00597.hp1 HG01358.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(502): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(480): Show |
1 | a0001c0001t0003g0179 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(485): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(511): Show |
1 | a0001c0001t0007g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(516): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(529): Show |
1 | a0011c0033t0003g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(534): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(494): Show |
1 | a0001c0001t0003g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(499): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(519): Show |
1 | a0001c0001t0002g0148 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(524): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(518): Show |
1 | a0001c0001t0002g0181 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(523): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(497): Show |
1 | a0001c0001t0002g0029 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(502): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(499): Show |
1 | a0001c0001t0002g0161 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(504): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(450): Show |
4 | a0007c0008t0005g0130 a0007c0008t0005g0131 a0007c0008t0005g0132 others(1): Show |
4 | HG02559.hp1 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(455): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(486): Show |
11 | a0001c0001t0001g0031 a0001c0001t0001g0145 a0001c0001t0001g0153 others(8): Show |
11 | HG00099.hp1 HG00642.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(491): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(497): Show |
1 | a0001c0001t0003g0152 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(502): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(488): Show |
1 | a0001c0001t0002g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(493): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(482): Show |
1 | a0002c0002t0001g0201 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(487): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(511): Show |
1 | a0001c0001t0001g0240 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(516): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(542): Show |
1 | a0002c0002t0001g0210 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(547): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(497): Show |
1 | a0002c0002t0002g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(502): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(474): Show |
1 | a0001c0001t0016g0195 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(479): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(489): Show |
1 | a0002c0002t0009g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(494): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(473): Show |
3 | a0001c0001t0002g0068 a0001c0001t0002g0246 a0001c0001t0016g0103 |
3 | HG00741.hp2 HG01123.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(478): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(568): Show |
1 | a0001c0001t0002g0104 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(573): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(508): Show |
2 | a0001c0001t0007g0105 a0016c0034t0005g0088 |
2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(513): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(483): Show |
1 | a0001c0001t0003g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(488): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(449): Show |
1 | a0001c0001t0003g0002 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(454): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(472): Show |
2 | a0001c0001t0001g0133 a0001c0001t0007g0069 |
2 | HG02970.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(477): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(447): Show |
1 | a0001c0001t0003g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(452): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(487): Show |
1 | a0013c0028t0016g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(492): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(511): Show |
1 | a0022c0032t0001g0064 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(516): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(486): Show |
4 | a0001c0001t0001g0123 a0001c0001t0013g0110 a0002c0002t0003g0109 others(1): Show |
4 | HG00609.hp2 HG01081.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(491): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(500): Show |
2 | a0001c0001t0001g0156 a0004c0004t0004g0125 |
2 | NA18954.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(505): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(488): Show |
1 | a0002c0010t0005g0111 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(493): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(497): Show |
1 | a0002c0002t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(502): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(488): Show |
1 | a0002c0002t0001g0070 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(493): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(530): Show |
1 | a0005c0005t0004g0212 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(535): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(457): Show |
1 | a0002c0002t0001g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(462): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(546): Show |
1 | a0002c0002t0002g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(551): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(521): Show |
1 | a0002c0002t0001g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(526): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(496): Show |
9 | a0002c0002t0001g0001 a0002c0002t0001g0142 a0002c0002t0001g0198 others(6): Show |
9 | HG01071.hp1 HG01496.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(501): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(471): Show |
2 | a0001c0001t0001g0241 a0002c0002t0003g0071 |
2 | HG01243.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(476): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(446): Show |
1 | a0002c0002t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(451): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(512): Show |
1 | a0002c0002t0003g0129 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(517): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(512): Show |
1 | a0002c0002t0001g0216 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(517): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(511): Show |
1 | a0002c0002t0009g0229 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(516): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(510): Show |
10 | a0001c0001t0001g0230 a0002c0002t0001g0085 a0002c0002t0001g0217 others(7): Show |
10 | HG00597.hp2 HG01952.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(515): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(485): Show |
6 | a0002c0002t0001g0072 a0002c0002t0001g0223 a0002c0002t0006g0112 others(3): Show |
6 | HG01099.hp1 HG02293.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(490): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(526): Show |
2 | a0002c0002t0001g0199 a0005c0005t0004g0231 |
2 | HG04199.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(531): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(524): Show |
1 | a0002c0002t0001g0114 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(529): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(499): Show |
4 | a0002c0002t0002g0074 a0002c0002t0006g0092 a0002c0002t0006g0097 others(1): Show |
4 | HG01928.hp1 HG01975.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(504): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(540): Show |
1 | a0002c0002t0002g0224 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(545): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(503): Show |
1 | a0002c0002t0001g0200 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(508): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(476): Show |
2 | a0002c0002t0001g0075 a0005c0005t0004g0116 |
2 | HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(481): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(479): Show |
1 | a0002c0002t0001g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(484): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(470): Show |
2 | a0001c0001t0009g0243 a0004c0004t0004g0244 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(475): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(498): Show |
1 | a0004c0004t0004g0238 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(503): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(475): Show |
1 | a0002c0002t0001g0117 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(480): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(483): Show |
1 | a0002c0002t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(488): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(474): Show |
1 | a0001c0001t0001g0126 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(479): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(485): Show |
1 | a0002c0002t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(490): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(510): Show |
1 | a0002c0002t0009g0202 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(515): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(525): Show |
1 | a0001c0001t0001g0155 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(530): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(500): Show |
1 | a0002c0002t0002g0062 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(505): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(495): Show |
1 | a0001c0001t0003g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(500): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(450): Show |
1 | a0001c0001t0001g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(455): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(475): Show |
2 | a0001c0001t0013g0119 a0004c0004t0004g0128 |
2 | NA18960.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(480): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(506): Show |
1 | a0002c0002t0001g0139 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(511): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(501): Show |
1 | a0002c0002t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(506): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(503): Show |
1 | a0002c0002t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(508): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(502): Show |
1 | a0002c0027t0005g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(507): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(500): Show |
1 | a0005c0005t0004g0136 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(505): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(470): Show |
1 | a0010c0012t0001g0077 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(475): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(457): Show |
1 | a0002c0002t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(462): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(486): Show |
1 | a0010c0012t0001g0120 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(491): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(485): Show |
2 | a0009c0011t0002g0080 a0010c0012t0004g0079 |
2 | HG00438.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(490): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(499): Show |
1 | a0009c0011t0006g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(504): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(461): Show |
1 | a0002c0002t0001g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(466): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(487): Show |
1 | a0002c0002t0006g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(492): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(468): Show |
1 | a0003c0003t0012g0026 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(473): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(491): Show |
1 | a0009c0011t0001g0083 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(496): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(522): Show |
1 | a0001c0001t0013g0084 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(527): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(481): Show |
1 | a0002c0002t0001g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(486): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(510): Show |
1 | a0005c0005t0004g0203 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(515): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(490): Show |
1 | a0020c0031t0001g0146 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.53-445_53-444insTC others(495): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCCTCTCC others(548): Show |
1 | a0005c0005t0004g0225 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.53-446_53-445insTC others(553): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253198 | T | TCTCTCTC others(502): Show |
1 | a0002c0002t0006g0093 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.53-452_53-451insTC others(507): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253198 | ||||||
| chr10:114253201 | T | TCTCCCCT others(344): Show |
1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(349): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253201 | ||||||
| chr10:114253202 | C | CCTCCCCC others(451): Show |
1 | a0001c0001t0001g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.53-449_53-448insCT others(456): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253202 | |||||||
| chr10:114253203 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.53-448T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253203 | |||||||
| chr10:114253205 | C | CCCTCCCC others(507): Show |
1 | a0002c0002t0001g0228 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(512): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253205 | ||||||
| chr10:114253208 | T | C | 1 | a0001c0001t0007g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.53-443T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253208 | |||||||
| chr10:114253208 | T | TCCCCCTC others(468): Show |
1 | a0003c0003t0017g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(473): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(558): Show |
2 | a0001c0001t0022g0158 a0001c0001t0030g0159 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.53-442_53-441insCC others(563): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(514): Show |
1 | a0001c0001t0003g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(519): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(442): Show |
1 | a0001c0001t0001g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(447): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(477): Show |
1 | a0004c0004t0004g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(482): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(503): Show |
1 | a0025c0029t0023g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(508): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(552): Show |
1 | a0001c0001t0001g0102 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(557): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(466): Show |
1 | a0004c0004t0004g0065 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(471): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(496): Show |
1 | a0002c0002t0009g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(501): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(467): Show |
1 | a0004c0004t0004g0127 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(472): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(586): Show |
1 | a0006c0006t0015g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(591): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253208 | T | TCCCCCTC others(585): Show |
4 | a0003c0003t0010g0050 a0003c0003t0025g0051 a0006c0006t0015g0049 others(1): Show |
4 | HG00738.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-442_53-441insCC others(590): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253208 | ||||||
| chr10:114253209 | C | CCCCCTCC others(421): Show |
1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(426): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253209 | |||||||
| chr10:114253209 | C | CCCCCTCC others(437): Show |
1 | a0003c0013t0012g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(442): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253209 | |||||||
| chr10:114253209 | C | CCCCCTCC others(489): Show |
1 | a0001c0001t0022g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(494): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253209 | |||||||
| chr10:114253209 | C | CCCCCTCC others(505): Show |
1 | a0001c0001t0002g0167 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(510): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253209 | |||||||
| chr10:114253209 | C | CCCCCTCC others(477): Show |
1 | a0001c0001t0013g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.53-442_53-441insCC others(482): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253209 | |||||||
| chr10:114253209 | C | CCCCCTCC others(499): Show |
1 | a0002c0002t0002g0141 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(504): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253209 | |||||||
| chr10:114253209 | C | CCCCCTCC others(588): Show |
1 | a0003c0003t0038g0048 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.53-442_53-441insCC others(593): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253209 | |||||||
| chr10:114253210 | T | C | 9 | a0001c0001t0001g0242 a0001c0001t0002g0167 a0001c0001t0013g0236 others(6): Show |
9 | HG01109.hp2 HG01975.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.53-441T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253210 | |||||||
| chr10:114253211 | C | CCCTCCCC others(470): Show |
1 | a0001c0001t0001g0242 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.53-438_53-437insTC others(475): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253211 | ||||||
| chr10:114253211 | C | T | 3 | a0001c0001t0001g0102 a0004c0004t0004g0065 a0004c0004t0004g0188 |
3 | NA18983.hp2 NA18999.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.53-440C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253211 | |||||||
| chr10:114253215 | C | CT | 7 | a0001c0001t0001g0174 a0001c0001t0022g0158 a0001c0001t0030g0159 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-436_53-435insT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253215 | |||||||
| chr10:114253215 | C | CTCCCCAT others(516): Show |
1 | a0001c0001t0007g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.53-436_53-435insTC others(521): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253215 | |||||||
| chr10:114253219 | C | T | 7 | a0001c0001t0007g0086 a0001c0001t0022g0158 a0001c0001t0030g0159 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-432C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253219 | |||||||
| chr10:114253221 | C | T | 1 | a0004c0004t0004g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.53-430C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253221 | |||||||
| chr10:114253222 | G | C | 240 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(237): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.53-429G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253222 | |||||||
| chr10:114253222 | G | T | 1 | a0005c0005t0004g0196 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.53-429G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253222 | |||||||
| chr10:114253223 | T | C | 1 | a0005c0005t0004g0196 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.53-428T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253223 | |||||||
| chr10:114253224 | C | CT | 6 | a0003c0003t0010g0050 a0003c0003t0025g0051 a0003c0003t0038g0048 others(3): Show |
6 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-427_53-426insT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253224 | |||||||
| chr10:114253224 | C | T | 1 | a0002c0002t0002g0062 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.53-427C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253224 | |||||||
| chr10:114253226 | C | T | 6 | a0003c0003t0010g0050 a0003c0003t0025g0051 a0003c0003t0038g0048 others(3): Show |
6 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-425C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253226 | |||||||
| chr10:114253228 | C | CTCCCCTC others(550): Show |
1 | a0001c0001t0031g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.53-423_53-422insTC others(555): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253228 | |||||||
| chr10:114253228 | C | T | 1 | a0004c0004t0004g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.53-423C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253228 | |||||||
| chr10:114253230 | T | C | 2 | a0003c0003t0019g0028 a0003c0003t0040g0057 |
2 | HG01175.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.53-421T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253230 | |||||||
| chr10:114253231 | C | T | 1 | a0003c0003t0040g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53-420C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253231 | |||||||
| chr10:114253235 | G | C | 241 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.53-416G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253235 | |||||||
| chr10:114253235 | G | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-416G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253235 | |||||||
| chr10:114253236 | T | C | 1 | a0004c0004t0004g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.53-415T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253236 | |||||||
| chr10:114253236 | T | TCCCTCCC others(538): Show |
1 | a0005c0005t0004g0196 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.53-414_53-413insCC others(543): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253236 | ||||||
| chr10:114253237 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-414C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253237 | |||||||
| chr10:114253238 | T | C | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-413T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253238 | |||||||
| chr10:114253240 | T | C | 4 | a0001c0001t0031g0144 a0001c0035t0003g0046 a0002c0002t0001g0228 others(1): Show |
4 | HG02145.hp2 HG03516.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-411T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253240 | |||||||
| chr10:114253243 | C | T | 2 | a0002c0002t0009g0229 a0005c0005t0001g0204 |
2 | HG01358.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.53-408C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253243 | |||||||
| chr10:114253244 | T | C | 5 | a0001c0001t0001g0239 a0001c0001t0031g0144 a0002c0002t0009g0229 others(2): Show |
5 | HG01358.hp2 HG02970.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-407T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253244 | |||||||
| chr10:114253245 | C | T | 1 | a0001c0001t0031g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.53-406C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253245 | |||||||
| chr10:114253246 | C | T | 1 | a0005c0005t0004g0196 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.53-405C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253246 | |||||||
| chr10:114253250 | G | C | 241 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.53-401G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253250 | |||||||
| chr10:114253250 | G | T | 1 | a0005c0005t0001g0204 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.53-401G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253250 | |||||||
| chr10:114253251 | T | C | 3 | a0001c0001t0001g0030 a0005c0005t0001g0204 a0023c0026t0004g0237 |
3 | HG01928.hp2 NA19000.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.53-400T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253251 | |||||||
| chr10:114253252 | C | T | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-399C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253252 | |||||||
| chr10:114253256 | G | C | 242 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.53-395G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253256 | |||||||
| chr10:114253257 | T | A | 1 | a0002c0002t0009g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.53-394T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253257 | |||||||
| chr10:114253257 | T | C | 1 | a0023c0026t0004g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.53-394T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253257 | |||||||
| chr10:114253264 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-387C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253264 | |||||||
| chr10:114253266 | T | C | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-385T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253266 | |||||||
| chr10:114253269 | T | C | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-382T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253269 | |||||||
| chr10:114253277 | A | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-374A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253277 | |||||||
| chr10:114253278 | C | T | 1 | a0003c0003t0012g0025 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.53-373C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253278 | |||||||
| chr10:114253279 | T | TC | 11 | a0001c0001t0001g0230 a0001c0001t0002g0161 a0001c0001t0003g0179 others(8): Show |
11 | HG00642.hp2 HG00735.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-366dupC | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 114253279 | ||||||
| chr10:114253313 | C | A | 1 | a0002c0002t0001g0199 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.53-338C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253313 | |||||||
| chr10:114253342 | C | T | 13 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(10): Show |
13 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.53-309C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253342 | |||||||
| chr10:114253343 | G | A | 1 | a0003c0007t0014g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.53-308G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253343 | |||||||
| chr10:114253430 | A | G | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.53-221A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253430 | |||||||
| chr10:114253472 | G | T | 6 | a0003c0003t0010g0050 a0003c0003t0025g0051 a0003c0003t0038g0048 others(3): Show |
6 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-179G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253472 | |||||||
| chr10:114253500 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.53-151C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253500 | |||||||
| chr10:114253553 | C | A | 5 | a0003c0003t0040g0057 a0008c0009t0010g0055 a0008c0009t0010g0056 others(2): Show |
5 | HG00280.hp1 HG01123.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-98C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253553 | |||||||
| chr10:114253608 | CT | C | 58 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(55): Show |
58 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.53-42delT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 2/13 | chr10 | 114253608 | |||||||
| chr10:114253817 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.127+92G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114253817 | |||||||
| chr10:114253818 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.127+93C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114253818 | |||||||
| chr10:114253824 | T | C | 1 | a0001c0001t0007g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.127+99T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114253824 | |||||||
| chr10:114253892 | T | C | 1 | a0002c0002t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127+167T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114253892 | |||||||
| chr10:114254033 | A | G | 29 | a0003c0003t0010g0019 a0003c0003t0010g0047 a0003c0003t0010g0050 others(26): Show |
29 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.127+308A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114254033 | |||||||
| chr10:114254239 | T | C | 2 | a0001c0001t0022g0158 a0001c0001t0030g0159 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.127+514T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114254239 | |||||||
| chr10:114254315 | G | A | 1 | a0002c0002t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.127+590G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114254315 | |||||||
| chr10:114254318 | C | T | 2 | a0002c0002t0001g0223 a0005c0005t0004g0222 |
2 | NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.127+593C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114254318 | |||||||
| chr10:114254347 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.128-568C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114254347 | |||||||
| chr10:114254600 | G | A | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.128-315G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114254600 | |||||||
| chr10:114254732 | G | A | 7 | a0003c0003t0024g0003 a0003c0007t0014g0006 a0003c0007t0014g0007 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-183G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114254732 | |||||||
| chr10:114254764 | C | A | 1 | a0008c0009t0010g0058 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.128-151C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 3/13 | chr10 | 114254764 | |||||||
| chr10:114255068 | G | T | 26 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(23): Show |
26 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.261+20G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255068 | |||||||
| chr10:114255136 | T | C | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.261+88T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255136 | |||||||
| chr10:114255137 | C | G | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.261+89C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255137 | |||||||
| chr10:114255186 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.261+138G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255186 | |||||||
| chr10:114255229 | C | CT | 7 | a0001c0001t0002g0170 a0001c0001t0003g0106 a0001c0001t0013g0236 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.261+194dupT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 114255229 | ||||||
| chr10:114255296 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.261+248C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255296 | |||||||
| chr10:114255567 | T | C | 1 | a0003c0003t0019g0032 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.261+519T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255567 | |||||||
| chr10:114255580 | G | A | 4 | a0002c0002t0001g0001 a0002c0002t0001g0134 a0002c0002t0001g0142 others(1): Show |
4 | HG01496.hp1 HG01496.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+532G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255580 | |||||||
| chr10:114255750 | G | T | 1 | a0001c0001t0001g0242 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.261+702G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255750 | |||||||
| chr10:114255771 | A | AT | 31 | a0001c0001t0022g0158 a0001c0001t0030g0159 a0002c0002t0001g0228 others(28): Show |
31 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.261+734dupT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 114255771 | ||||||
| chr10:114255771 | AT | A | 53 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(50): Show |
53 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.261+734delT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 114255771 | ||||||
| chr10:114255792 | A | G | 1 | a0003c0003t0010g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.261+744A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255792 | |||||||
| chr10:114255897 | C | T | 1 | a0002c0002t0001g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.261+849C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255897 | |||||||
| chr10:114255931 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.261+883G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114255931 | |||||||
| chr10:114256047 | C | T | 3 | a0003c0007t0014g0006 a0003c0007t0014g0007 a0003c0007t0014g0008 |
3 | HG02280.hp2 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.261+999C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256047 | |||||||
| chr10:114256053 | G | T | 1 | a0001c0001t0002g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.261+1005G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256053 | |||||||
| chr10:114256478 | G | A | 1 | a0003c0007t0014g0006 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.261+1430G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256478 | |||||||
| chr10:114256498 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.261+1450A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256498 | |||||||
| chr10:114256527 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.261+1479C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256527 | |||||||
| chr10:114256593 | T | G | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1545T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256593 | |||||||
| chr10:114256595 | A | T | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1547A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256595 | |||||||
| chr10:114256603 | C | G | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1555C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256603 | |||||||
| chr10:114256607 | A | G | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1559A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256607 | |||||||
| chr10:114256609 | T | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1561T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256609 | |||||||
| chr10:114256612 | A | T | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1564A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256612 | |||||||
| chr10:114256614 | T | C | 1 | a0005c0005t0004g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.261+1566T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256614 | |||||||
| chr10:114256615 | T | A | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1567T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256615 | |||||||
| chr10:114256618 | A | G | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1570A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256618 | |||||||
| chr10:114256620 | A | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1572A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256620 | |||||||
| chr10:114256624 | A | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1576A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256624 | |||||||
| chr10:114256625 | G | T | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1577G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256625 | |||||||
| chr10:114256626 | A | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1578A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256626 | |||||||
| chr10:114256627 | G | T | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1579G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256627 | |||||||
| chr10:114256628 | A | G | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1580A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256628 | |||||||
| chr10:114256632 | T | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1584T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256632 | |||||||
| chr10:114256634 | T | G | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1586T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256634 | |||||||
| chr10:114256638 | C | T | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1590C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256638 | |||||||
| chr10:114256644 | G | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1596G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256644 | |||||||
| chr10:114256648 | C | T | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1600C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256648 | |||||||
| chr10:114256663 | T | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1615T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256663 | |||||||
| chr10:114256668 | A | T | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1620A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256668 | |||||||
| chr10:114256713 | G | A | 136 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(133): Show |
136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.261+1665G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256713 | |||||||
| chr10:114256714 | T | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1666T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256714 | |||||||
| chr10:114256716 | C | A | 2 | a0003c0013t0012g0041 a0017c0017t0027g0040 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.261+1668C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256716 | |||||||
| chr10:114256716 | C | G | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1668C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256716 | |||||||
| chr10:114256721 | T | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1673T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256721 | |||||||
| chr10:114256724 | C | T | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1676C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256724 | |||||||
| chr10:114256730 | G | A | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1682G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256730 | |||||||
| chr10:114256736 | T | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1688T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256736 | |||||||
| chr10:114256758 | A | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1710A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256758 | |||||||
| chr10:114256778 | C | G | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1730C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256778 | |||||||
| chr10:114256805 | A | G | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+1757A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256805 | |||||||
| chr10:114256832 | C | T | 8 | a0001c0001t0003g0002 a0001c0001t0003g0106 a0001c0001t0003g0107 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.261+1784C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256832 | |||||||
| chr10:114256834 | C | T | 1 | a0001c0001t0007g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.261+1786C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256834 | |||||||
| chr10:114256904 | C | T | 2 | a0003c0003t0025g0011 a0003c0003t0039g0012 |
2 | HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.261+1856C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256904 | |||||||
| chr10:114256909 | C | CA | 33 | a0001c0001t0001g0154 a0001c0001t0001g0186 a0001c0001t0002g0176 others(30): Show |
33 | HG00597.hp2 HG00609.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.261+1884dupA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 114256909 | ||||||
| chr10:114256909 | C | CAA | 13 | a0001c0001t0002g0063 a0001c0001t0022g0158 a0001c0001t0030g0159 others(10): Show |
13 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.261+1883_261+1884d others(4): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 114256909 | ||||||
| chr10:114256909 | CA | C | 17 | a0001c0001t0001g0156 a0001c0001t0002g0167 a0001c0001t0003g0150 others(14): Show |
17 | HG00099.hp2 HG00438.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.261+1884delA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 114256909 | ||||||
| chr10:114256909 | CAAAAA | C | 6 | a0003c0003t0017g0014 a0003c0003t0018g0234 a0003c0003t0018g0235 others(3): Show |
6 | HG01099.hp2 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+1880_261+1884d others(7): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 114256909 | ||||||
| chr10:114256925 | A | T | 1 | a0003c0020t0020g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.261+1877A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256925 | |||||||
| chr10:114256932 | AT | A | 14 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0024g0003 others(11): Show |
14 | HG01074.hp2 HG01361.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.261+1886delT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 114256932 | ||||||
| chr10:114256933 | T | A | 9 | a0003c0003t0019g0028 a0003c0003t0019g0032 a0003c0013t0012g0157 others(6): Show |
9 | HG01106.hp2 HG01175.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+1885T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114256933 | |||||||
| chr10:114257531 | C | T | 1 | a0001c0001t0031g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.261+2483C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114257531 | |||||||
| chr10:114257735 | T | C | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+2687T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114257735 | |||||||
| chr10:114257736 | G | T | 1 | a0003c0003t0011g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+2688G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114257736 | |||||||
| chr10:114258162 | T | G | 61 | a0001c0001t0022g0158 a0001c0001t0030g0159 a0001c0001t0031g0144 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.262-3024T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114258162 | |||||||
| chr10:114258894 | G | A | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.262-2292G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114258894 | |||||||
| chr10:114259013 | C | T | 1 | a0002c0002t0001g0199 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.262-2173C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114259013 | |||||||
| chr10:114259186 | A | T | 119 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(116): Show |
119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.262-2000A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114259186 | |||||||
| chr10:114259473 | T | G | 1 | a0006c0006t0008g0034 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.262-1713T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114259473 | |||||||
| chr10:114259486 | A | T | 1 | a0001c0001t0002g0232 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.262-1700A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114259486 | |||||||
| chr10:114259537 | T | C | 1 | a0003c0003t0025g0011 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.262-1649T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114259537 | |||||||
| chr10:114259839 | A | G | 59 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(56): Show |
59 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.262-1347A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114259839 | |||||||
| chr10:114259939 | G | A | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.262-1247G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114259939 | |||||||
| chr10:114259996 | C | G | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.262-1190C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114259996 | |||||||
| chr10:114260316 | C | T | 6 | a0003c0003t0010g0047 a0003c0003t0040g0057 a0008c0009t0010g0055 others(3): Show |
6 | HG00280.hp1 HG01123.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-870C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114260316 | |||||||
| chr10:114260337 | G | A | 1 | a0002c0002t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.262-849G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114260337 | |||||||
| chr10:114260389 | A | G | 61 | a0001c0001t0022g0158 a0001c0001t0030g0159 a0001c0001t0031g0144 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.262-797A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114260389 | |||||||
| chr10:114260451 | T | C | 1 | a0003c0003t0024g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.262-735T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114260451 | |||||||
| chr10:114260571 | G | A | 2 | a0001c0001t0022g0158 a0001c0001t0030g0159 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.262-615G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114260571 | |||||||
| chr10:114260681 | G | C | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.262-505G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114260681 | |||||||
| chr10:114260723 | G | C | 1 | a0019c0015t0028g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.262-463G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114260723 | |||||||
| chr10:114260729 | G | A | 2 | a0001c0001t0001g0126 a0004c0004t0004g0125 |
2 | HG00408.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.262-457G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114260729 | |||||||
| chr10:114260973 | A | C | 1 | a0003c0020t0020g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.262-213A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114260973 | |||||||
| chr10:114261177 | C | G | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.262-9C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 4/13 | chr10 | 114261177 | |||||||
| chr10:114261404 | G | A | 1 | a0001c0001t0013g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.371+109G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114261404 | |||||||
| chr10:114261454 | A | G | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+159A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114261454 | |||||||
| chr10:114261973 | G | A | 2 | a0003c0013t0012g0041 a0017c0017t0027g0040 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.371+678G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114261973 | |||||||
| chr10:114261994 | G | A | 119 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(116): Show |
119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.371+699G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114261994 | |||||||
| chr10:114262046 | C | T | 14 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(11): Show |
14 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.371+751C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262046 | |||||||
| chr10:114262065 | G | A | 1 | a0017c0017t0027g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.371+770G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262065 | |||||||
| chr10:114262180 | G | A | 1 | a0001c0001t0013g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.371+885G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262180 | |||||||
| chr10:114262240 | A | G | 60 | a0001c0001t0022g0158 a0001c0001t0030g0159 a0001c0001t0031g0144 others(57): Show |
60 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.371+945A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262240 | |||||||
| chr10:114262248 | A | G | 13 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(10): Show |
13 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.371+953A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262248 | |||||||
| chr10:114262321 | T | C | 1 | a0003c0003t0017g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.371+1026T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262321 | |||||||
| chr10:114262343 | T | C | 120 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(117): Show |
120 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.371+1048T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262343 | |||||||
| chr10:114262356 | A | G | 3 | a0003c0013t0012g0157 a0015c0018t0021g0043 a0019c0015t0028g0042 |
3 | HG02647.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.371+1061A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262356 | |||||||
| chr10:114262378 | A | C | 1 | a0003c0003t0024g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.371+1083A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262378 | |||||||
| chr10:114262875 | C | T | 1 | a0009c0011t0006g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.371+1580C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262875 | |||||||
| chr10:114262994 | G | C | 138 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.371+1699G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114262994 | |||||||
| chr10:114263023 | G | A | 1 | a0001c0001t0003g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.371+1728G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263023 | |||||||
| chr10:114263083 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.371+1788T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263083 | |||||||
| chr10:114263114 | C | G | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.371+1819C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263114 | |||||||
| chr10:114263204 | G | A | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+1909G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263204 | |||||||
| chr10:114263232 | C | G | 5 | a0003c0003t0040g0057 a0008c0009t0010g0055 a0008c0009t0010g0056 others(2): Show |
5 | HG00280.hp1 HG01123.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.371+1937C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263232 | |||||||
| chr10:114263328 | A | AT | 100 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.371+2057dupT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114263328 | ||||||
| chr10:114263328 | A | ATT | 24 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0177 others(21): Show |
24 | HG00735.hp1 HG01081.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.371+2056_371+2057d others(4): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114263328 | ||||||
| chr10:114263328 | A | T | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+2033A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263328 | |||||||
| chr10:114263493 | C | T | 3 | a0003c0013t0012g0157 a0015c0018t0021g0043 a0019c0015t0028g0042 |
3 | HG02647.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.371+2198C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263493 | |||||||
| chr10:114263522 | C | A | 61 | a0001c0001t0022g0158 a0001c0001t0030g0159 a0001c0001t0031g0144 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.371+2227C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263522 | |||||||
| chr10:114263561 | T | A | 3 | a0002c0002t0002g0218 a0002c0002t0002g0221 a0005c0005t0004g0212 |
3 | HG01952.hp2 HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.371+2266T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263561 | |||||||
| chr10:114263574 | T | A | 1 | a0005c0005t0004g0196 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.371+2279T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263574 | |||||||
| chr10:114263583 | C | T | 1 | a0003c0003t0024g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.371+2288C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263583 | |||||||
| chr10:114263671 | C | T | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+2376C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263671 | |||||||
| chr10:114263872 | A | G | 6 | a0003c0007t0014g0006 a0003c0007t0014g0007 a0003c0007t0014g0008 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.371+2577A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114263872 | |||||||
| chr10:114264387 | GCATAGCA others(3): Show |
G | 14 | a0001c0001t0031g0144 a0003c0003t0010g0047 a0003c0003t0010g0050 others(11): Show |
14 | HG00280.hp1 HG00738.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.371+3097_371+3106d others(12): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114264387 | ||||||
| chr10:114264423 | CT | C | 55 | a0001c0001t0009g0067 a0001c0001t0022g0158 a0001c0001t0030g0159 others(52): Show |
55 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.371+3140delT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114264423 | ||||||
| chr10:114264442 | G | T | 1 | a0001c0001t0001g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.371+3147G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114264442 | |||||||
| chr10:114264578 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.371+3283C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114264578 | |||||||
| chr10:114264591 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.371+3296T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114264591 | |||||||
| chr10:114264687 | G | C | 1 | a0002c0002t0001g0228 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371+3392G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114264687 | |||||||
| chr10:114264699 | G | A | 33 | a0001c0001t0022g0158 a0001c0001t0030g0159 a0001c0001t0031g0144 others(30): Show |
33 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.371+3404G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114264699 | |||||||
| chr10:114264758 | C | T | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+3463C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114264758 | |||||||
| chr10:114264865 | G | A | 6 | a0003c0003t0010g0050 a0003c0003t0025g0051 a0003c0003t0038g0048 others(3): Show |
6 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.371+3570G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114264865 | |||||||
| chr10:114264947 | T | C | 1 | a0002c0002t0006g0097 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.371+3652T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114264947 | |||||||
| chr10:114265040 | G | A | 1 | a0008c0009t0010g0056 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.371+3745G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114265040 | |||||||
| chr10:114265241 | TTTATG | T | 4 | a0001c0001t0002g0167 a0001c0001t0002g0172 a0001c0001t0002g0176 others(1): Show |
4 | HG01934.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+3953_371+3957d others(7): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114265241 | ||||||
| chr10:114265424 | A | G | 5 | a0002c0002t0001g0098 a0002c0002t0003g0071 a0002c0010t0005g0073 others(2): Show |
5 | HG01243.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.371+4129A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114265424 | |||||||
| chr10:114265511 | T | C | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.371+4216T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114265511 | |||||||
| chr10:114265522 | A | C | 1 | a0003c0003t0017g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.371+4227A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114265522 | |||||||
| chr10:114265563 | A | G | 116 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.371+4268A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114265563 | |||||||
| chr10:114265624 | G | A | 1 | a0002c0002t0002g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.371+4329G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114265624 | |||||||
| chr10:114265998 | T | C | 1 | a0001c0001t0009g0243 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.371+4703T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114265998 | |||||||
| chr10:114266158 | G | A | 1 | a0025c0029t0023g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.371+4863G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266158 | |||||||
| chr10:114266252 | G | A | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.371+4957G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266252 | |||||||
| chr10:114266533 | G | A | 5 | a0001c0001t0002g0068 a0001c0001t0009g0067 a0001c0001t0016g0103 others(2): Show |
5 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.371+5238G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266533 | |||||||
| chr10:114266730 | G | A | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+5435G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266730 | |||||||
| chr10:114266745 | G | GT | 3 | a0002c0002t0001g0200 a0002c0002t0001g0214 a0002c0002t0033g0220 |
3 | HG00738.hp2 HG01952.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.371+5453dupT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114266745 | ||||||
| chr10:114266752 | G | A | 3 | a0001c0001t0002g0170 a0001c0001t0003g0150 a0001c0001t0007g0173 |
3 | HG02257.hp1 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.371+5457G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266752 | |||||||
| chr10:114266770 | C | T | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+5475C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266770 | |||||||
| chr10:114266829 | G | A | 3 | a0001c0001t0022g0158 a0001c0001t0030g0159 a0005c0005t0004g0196 |
3 | HG01884.hp1 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.371+5534G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266829 | |||||||
| chr10:114266834 | C | A | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.371+5539C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266834 | |||||||
| chr10:114266847 | T | G | 31 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(28): Show |
31 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.371+5552T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266847 | |||||||
| chr10:114266899 | T | C | 1 | a0003c0003t0038g0048 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.371+5604T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114266899 | |||||||
| chr10:114267073 | A | C | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372-5667A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114267073 | |||||||
| chr10:114267282 | A | G | 2 | a0001c0001t0003g0066 a0001c0001t0007g0100 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.372-5458A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114267282 | |||||||
| chr10:114267409 | G | A | 2 | a0001c0001t0003g0002 a0001c0001t0003g0107 |
2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.372-5331G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114267409 | |||||||
| chr10:114267598 | A | AT | 33 | a0001c0035t0003g0046 a0003c0003t0010g0019 a0003c0003t0011g0015 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.372-5127dupT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114267598 | ||||||
| chr10:114267598 | A | ATT | 21 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(18): Show |
21 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.372-5128_372-5127d others(4): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114267598 | ||||||
| chr10:114267638 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.372-5102C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114267638 | |||||||
| chr10:114267684 | C | T | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372-5056C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114267684 | |||||||
| chr10:114267796 | C | G | 13 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(10): Show |
13 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.372-4944C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114267796 | |||||||
| chr10:114268199 | C | T | 60 | a0001c0001t0001g0241 a0001c0001t0013g0110 a0001c0001t0013g0119 others(57): Show |
60 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.372-4541C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268199 | |||||||
| chr10:114268375 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.372-4365C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268375 | |||||||
| chr10:114268576 | G | A | 107 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(104): Show |
107 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.372-4164G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268576 | |||||||
| chr10:114268578 | C | T | 1 | a0003c0003t0017g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.372-4162C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268578 | |||||||
| chr10:114268675 | G | A | 2 | a0001c0001t0022g0158 a0001c0001t0030g0159 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.372-4065G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268675 | |||||||
| chr10:114268691 | CTTTTTTC others(6): Show |
C | 7 | a0001c0001t0007g0086 a0002c0002t0003g0109 a0007c0008t0005g0089 others(4): Show |
7 | HG01081.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.372-4042_372-4030d others(15): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114268691 | ||||||
| chr10:114268698 | CT | C | 47 | a0001c0001t0001g0031 a0001c0001t0001g0145 a0001c0001t0001g0153 others(44): Show |
47 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.372-4028delT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114268698 | ||||||
| chr10:114268698 | CTTT | C | 7 | a0003c0007t0014g0006 a0003c0007t0014g0007 a0003c0007t0014g0008 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.372-4030_372-4028d others(5): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114268698 | ||||||
| chr10:114268701 | T | TTTTC | 51 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(48): Show |
51 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.372-4036_372-4035i others(6): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114268701 | ||||||
| chr10:114268705 | T | C | 1 | a0002c0002t0006g0115 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.372-4035T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268705 | |||||||
| chr10:114268722 | T | A | 1 | a0002c0002t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.372-4018T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268722 | |||||||
| chr10:114268746 | G | A | 2 | a0001c0001t0001g0166 a0025c0029t0023g0194 |
2 | HG03239.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.372-3994G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268746 | |||||||
| chr10:114268781 | G | T | 1 | a0003c0003t0038g0048 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.372-3959G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268781 | |||||||
| chr10:114268820 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.372-3920G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268820 | |||||||
| chr10:114268833 | G | T | 48 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(45): Show |
48 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.372-3907G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268833 | |||||||
| chr10:114268871 | A | G | 1 | a0005c0005t0004g0091 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.372-3869A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268871 | |||||||
| chr10:114268893 | T | C | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.372-3847T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268893 | |||||||
| chr10:114268955 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.372-3785A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114268955 | |||||||
| chr10:114269023 | TTTC | T | 57 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(54): Show |
57 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.372-3712_372-3710d others(5): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114269023 | ||||||
| chr10:114269051 | A | G | 3 | a0003c0013t0012g0157 a0015c0018t0021g0043 a0019c0015t0028g0042 |
3 | HG02647.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.372-3689A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114269051 | |||||||
| chr10:114269228 | C | T | 5 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-3512C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114269228 | |||||||
| chr10:114269883 | A | G | 3 | a0002c0002t0001g0076 a0002c0002t0001g0101 a0002c0002t0001g0114 |
3 | HG01069.hp1 HG01071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.372-2857A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114269883 | |||||||
| chr10:114269974 | A | G | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.372-2766A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114269974 | |||||||
| chr10:114270064 | A | G | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372-2676A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114270064 | |||||||
| chr10:114270184 | C | T | 1 | a0001c0001t0013g0084 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.372-2556C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114270184 | |||||||
| chr10:114270341 | C | G | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.372-2399C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114270341 | |||||||
| chr10:114270369 | T | C | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.372-2371T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114270369 | |||||||
| chr10:114270495 | G | A | 1 | a0001c0001t0031g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.372-2245G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114270495 | |||||||
| chr10:114271003 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.372-1737T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114271003 | |||||||
| chr10:114271014 | C | T | 234 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(231): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.372-1726C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114271014 | |||||||
| chr10:114271606 | A | AACACACA others(5): Show |
1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372-1133_372-1132i others(14): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271606 | ||||||
| chr10:114271608 | A | AAC | 31 | a0001c0001t0001g0126 a0001c0001t0002g0178 a0001c0001t0003g0149 others(28): Show |
31 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.372-1098_372-1097d others(4): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271608 | A | AACAC | 14 | a0001c0001t0003g0107 a0001c0035t0003g0046 a0002c0002t0009g0122 others(11): Show |
14 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.372-1100_372-1097d others(6): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271608 | A | AACACACA others(3): Show |
2 | a0001c0001t0022g0158 a0001c0001t0030g0159 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.372-1106_372-1097d others(12): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271608 | A | AACACACA others(7): Show |
2 | a0003c0003t0010g0047 a0003c0003t0017g0059 |
2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.372-1110_372-1097d others(16): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271608 | A | AACACACA others(9): Show |
1 | a0001c0001t0013g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.372-1112_372-1097d others(18): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271608 | A | AACACACA others(11): Show |
2 | a0001c0001t0031g0144 a0003c0003t0025g0051 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.372-1114_372-1097d others(20): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271608 | A | AACACACA others(13): Show |
1 | a0006c0006t0015g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.372-1116_372-1097d others(22): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271608 | A | AACACACA others(17): Show |
2 | a0003c0003t0010g0050 a0006c0006t0015g0052 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.372-1120_372-1097d others(26): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271608 | A | AACACACA others(19): Show |
2 | a0003c0003t0038g0048 a0006c0006t0015g0053 |
2 | HG00738.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.372-1122_372-1097d others(28): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271608 | A | C | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372-1132A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114271608 | |||||||
| chr10:114271608 | AAC | A | 16 | a0001c0001t0002g0170 a0001c0001t0003g0150 a0001c0001t0007g0173 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.372-1098_372-1097d others(4): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 114271608 | ||||||
| chr10:114271610 | C | A | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.372-1130C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114271610 | |||||||
| chr10:114271637 | A | G | 1 | a0003c0003t0018g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.372-1103A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114271637 | |||||||
| chr10:114271788 | G | T | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372-952G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114271788 | |||||||
| chr10:114271854 | G | A | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372-886G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114271854 | |||||||
| chr10:114271904 | C | T | 56 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(53): Show |
56 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.372-836C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114271904 | |||||||
| chr10:114272026 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.372-714C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114272026 | |||||||
| chr10:114272163 | C | T | 1 | a0011c0033t0003g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.372-577C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114272163 | |||||||
| chr10:114272219 | C | T | 1 | a0003c0003t0017g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.372-521C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114272219 | |||||||
| chr10:114272458 | C | G | 2 | a0002c0002t0001g0001 a0002c0002t0001g0142 |
2 | HG01496.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.372-282C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114272458 | |||||||
| chr10:114272463 | G | C | 1 | a0003c0003t0017g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.372-277G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114272463 | |||||||
| chr10:114272652 | A | G | 1 | a0002c0002t0001g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.372-88A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 5/13 | chr10 | 114272652 | |||||||
| chr10:114273393 | C | T | 1 | a0024c0030t0004g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.566+459C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114273393 | |||||||
| chr10:114273586 | T | G | 60 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(57): Show |
60 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.566+652T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114273586 | |||||||
| chr10:114273665 | C | T | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566+731C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114273665 | |||||||
| chr10:114273965 | A | G | 2 | a0002c0002t0001g0075 a0005c0005t0004g0116 |
2 | HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.566+1031A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114273965 | |||||||
| chr10:114274021 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.566+1087G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114274021 | |||||||
| chr10:114274044 | A | G | 4 | a0002c0002t0003g0071 a0002c0010t0005g0073 a0002c0010t0005g0111 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+1110A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114274044 | |||||||
| chr10:114274133 | C | T | 13 | a0003c0003t0012g0025 a0003c0003t0012g0026 a0003c0003t0019g0028 others(10): Show |
13 | HG01074.hp2 HG01106.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.566+1199C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114274133 | |||||||
| chr10:114274362 | G | A | 7 | a0002c0002t0001g0078 a0002c0002t0002g0227 a0009c0011t0001g0083 others(4): Show |
7 | HG00438.hp1 HG00673.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.566+1428G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114274362 | |||||||
| chr10:114274407 | A | G | 62 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.566+1473A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114274407 | |||||||
| chr10:114274457 | C | G | 1 | a0004c0004t0001g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.566+1523C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114274457 | |||||||
| chr10:114274560 | C | T | 16 | a0003c0003t0010g0019 a0003c0003t0011g0015 a0003c0003t0011g0017 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.566+1626C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114274560 | |||||||
| chr10:114274659 | CT | C | 8 | a0001c0001t0001g0156 a0002c0002t0001g0140 a0002c0002t0003g0109 others(5): Show |
8 | HG01081.hp2 HG02559.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.566+1739delT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114274659 | ||||||
| chr10:114274774 | C | T | 4 | a0003c0007t0014g0006 a0003c0007t0014g0007 a0003c0007t0014g0008 others(1): Show |
4 | HG02280.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+1840C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114274774 | |||||||
| chr10:114274958 | T | C | 1 | a0014c0021t0020g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.566+2024T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114274958 | |||||||
| chr10:114275000 | T | G | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.566+2066T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114275000 | |||||||
| chr10:114275115 | C | T | 45 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0145 others(42): Show |
45 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.566+2181C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114275115 | |||||||
| chr10:114275153 | G | C | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.566+2219G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114275153 | |||||||
| chr10:114275266 | C | A | 1 | a0002c0002t0003g0129 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.566+2332C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114275266 | |||||||
| chr10:114275387 | A | G | 2 | a0002c0002t0001g0094 a0002c0002t0002g0095 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.566+2453A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114275387 | |||||||
| chr10:114275494 | C | T | 5 | a0006c0006t0008g0033 a0006c0006t0008g0034 a0006c0006t0008g0035 others(2): Show |
5 | NA18945.hp2 NA18970.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.567-2420C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114275494 | |||||||
| chr10:114275558 | C | T | 37 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(34): Show |
37 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.567-2356C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114275558 | |||||||
| chr10:114275561 | A | ACTGT | 170 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(167): Show |
170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.567-2350_567-2349i others(6): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114275561 | ||||||
| chr10:114275586 | G | T | 62 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.567-2328G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114275586 | |||||||
| chr10:114275786 | G | A | 2 | a0001c0001t0003g0066 a0001c0001t0007g0100 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.567-2128G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114275786 | |||||||
| chr10:114276067 | T | C | 2 | a0002c0002t0001g0139 a0002c0002t0001g0140 |
2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.567-1847T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276067 | |||||||
| chr10:114276191 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.567-1723G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276191 | |||||||
| chr10:114276308 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.567-1606C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276308 | |||||||
| chr10:114276381 | G | T | 1 | a0003c0003t0024g0003 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.567-1533G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276381 | |||||||
| chr10:114276449 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.567-1465A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276449 | |||||||
| chr10:114276504 | C | G | 2 | a0001c0001t0013g0110 a0001c0001t0013g0119 |
2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.567-1410C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276504 | |||||||
| chr10:114276561 | C | T | 1 | a0002c0002t0001g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.567-1353C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276561 | |||||||
| chr10:114276562 | G | A | 2 | a0001c0001t0003g0002 a0001c0001t0003g0107 |
2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.567-1352G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276562 | |||||||
| chr10:114276673 | A | AT | 40 | a0001c0001t0001g0123 a0001c0001t0001g0145 a0001c0001t0001g0154 others(37): Show |
40 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.567-1215dupT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114276673 | ||||||
| chr10:114276673 | AT | A | 18 | a0001c0001t0013g0110 a0002c0002t0001g0001 a0002c0002t0001g0142 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.567-1215delT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114276673 | ||||||
| chr10:114276673 | ATT | A | 21 | a0003c0003t0010g0050 a0003c0003t0012g0025 a0003c0003t0012g0026 others(18): Show |
21 | HG01074.hp2 HG01106.hp2 HG02135.hp1 others(18): Show |
intron_variant | MODIFIER | c.567-1216_567-1215d others(4): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114276673 | ||||||
| chr10:114276673 | ATTT | A | 19 | a0001c0001t0022g0158 a0001c0001t0030g0159 a0001c0035t0003g0046 others(16): Show |
19 | HG00323.hp1 HG00642.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.567-1217_567-1215d others(5): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114276673 | ||||||
| chr10:114276750 | C | A | 1 | a0002c0002t0009g0229 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.567-1164C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276750 | |||||||
| chr10:114276919 | G | C | 1 | a0001c0001t0022g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.567-995G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276919 | |||||||
| chr10:114276950 | G | A | 1 | a0001c0001t0016g0195 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.567-964G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114276950 | |||||||
| chr10:114277095 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.567-819A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277095 | |||||||
| chr10:114277130 | A | G | 3 | a0002c0002t0001g0076 a0002c0002t0001g0101 a0002c0002t0001g0114 |
3 | HG01069.hp1 HG01071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.567-784A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277130 | |||||||
| chr10:114277161 | T | C | 1 | a0001c0001t0013g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.567-753T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277161 | |||||||
| chr10:114277162 | G | A | 2 | a0002c0010t0005g0111 a0002c0010t0005g0113 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.567-752G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277162 | |||||||
| chr10:114277165 | C | T | 1 | a0019c0015t0028g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.567-749C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277165 | |||||||
| chr10:114277166 | G | A | 3 | a0003c0013t0012g0157 a0015c0018t0021g0043 a0019c0015t0028g0042 |
3 | HG02647.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.567-748G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277166 | |||||||
| chr10:114277168 | C | CT | 44 | a0001c0001t0001g0030 a0001c0001t0001g0102 a0001c0001t0001g0126 others(41): Show |
44 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.567-716dupT | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114277168 | ||||||
| chr10:114277168 | C | CTTT | 8 | a0001c0001t0001g0123 a0002c0002t0032g0208 a0003c0003t0010g0050 others(5): Show |
8 | HG01099.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.567-718_567-716dup others(3): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114277168 | ||||||
| chr10:114277168 | C | CTTTT | 13 | a0002c0002t0001g0001 a0002c0002t0001g0142 a0003c0003t0010g0019 others(10): Show |
13 | HG00280.hp1 HG00323.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.567-719_567-716dup others(4): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114277168 | ||||||
| chr10:114277168 | C | CTTTTT | 12 | a0001c0001t0031g0144 a0003c0003t0011g0017 a0003c0003t0012g0025 others(9): Show |
12 | HG00642.hp2 HG01074.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.567-720_567-716dup others(5): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114277168 | ||||||
| chr10:114277168 | C | CTTTTTT | 17 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0003c0003t0012g0026 others(14): Show |
17 | HG01175.hp1 HG01361.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.567-721_567-716dup others(6): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114277168 | ||||||
| chr10:114277168 | CTTTTTTT others(8): Show |
C | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.567-730_567-716del others(15): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 114277168 | ||||||
| chr10:114277198 | T | C | 1 | a0010c0012t0001g0077 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.567-716T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277198 | |||||||
| chr10:114277357 | T | A | 7 | a0003c0003t0024g0003 a0003c0007t0014g0006 a0003c0007t0014g0007 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.567-557T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277357 | |||||||
| chr10:114277372 | T | C | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.567-542T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277372 | |||||||
| chr10:114277479 | C | A | 1 | a0002c0002t0002g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.567-435C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277479 | |||||||
| chr10:114277479 | C | T | 16 | a0003c0003t0010g0019 a0003c0003t0011g0015 a0003c0003t0011g0017 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.567-435C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277479 | |||||||
| chr10:114277480 | C | G | 62 | a0001c0001t0013g0110 a0001c0001t0013g0119 a0001c0001t0022g0158 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.567-434C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277480 | |||||||
| chr10:114277684 | A | G | 1 | a0002c0002t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.567-230A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277684 | |||||||
| chr10:114277725 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.567-189C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 6/13 | chr10 | 114277725 | |||||||
| chr10:114278053 | A | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0232 |
2 | HG00099.hp1 HG01106.hp1 |
splice_region_variant&intron_variant | LOW | c.700+6A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 7/13 | chr10 | 114278053 | |||||||
| chr10:114278083 | A | G | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.700+36A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 7/13 | chr10 | 114278083 | |||||||
| chr10:114278143 | T | G | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.700+96T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 7/13 | chr10 | 114278143 | |||||||
| chr10:114278197 | G | A | 1 | a0003c0013t0012g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.700+150G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 7/13 | chr10 | 114278197 | |||||||
| chr10:114278222 | T | C | 1 | a0002c0002t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.700+175T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 7/13 | chr10 | 114278222 | |||||||
| chr10:114278408 | G | A | 10 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(7): Show |
10 | HG00438.hp2 HG00673.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.701-311G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 7/13 | chr10 | 114278408 | |||||||
| chr10:114278875 | G | A | 1 | a0003c0020t0020g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.833+24G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114278875 | |||||||
| chr10:114278912 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.833+61C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114278912 | |||||||
| chr10:114279278 | T | C | 2 | a0001c0035t0003g0046 a0003c0016t0003g0060 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.833+427T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279278 | |||||||
| chr10:114279316 | C | T | 1 | a0004c0004t0004g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.833+465C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279316 | |||||||
| chr10:114279664 | T | C | 6 | a0003c0007t0014g0006 a0003c0007t0014g0007 a0003c0007t0014g0008 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.833+813T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279664 | |||||||
| chr10:114279702 | C | T | 2 | a0003c0013t0012g0041 a0017c0017t0027g0040 |
2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.833+851C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279702 | |||||||
| chr10:114279768 | C | T | 2 | a0003c0003t0012g0025 a0003c0003t0012g0026 |
2 | HG01074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.833+917C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279768 | |||||||
| chr10:114279770 | G | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.833+919G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279770 | |||||||
| chr10:114279777 | C | G | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.833+926C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279777 | |||||||
| chr10:114279847 | G | A | 2 | a0002c0002t0001g0200 a0002c0002t0033g0220 |
2 | HG00738.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.833+996G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279847 | |||||||
| chr10:114279874 | G | A | 1 | a0002c0014t0003g0205 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.833+1023G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279874 | |||||||
| chr10:114279898 | C | T | 1 | a0003c0003t0018g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.833+1047C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114279898 | |||||||
| chr10:114280022 | G | T | 1 | a0001c0001t0013g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.833+1171G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280022 | |||||||
| chr10:114280060 | C | T | 1 | a0001c0001t0007g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.833+1209C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280060 | |||||||
| chr10:114280071 | C | G | 3 | a0001c0001t0003g0171 a0001c0001t0003g0185 a0001c0001t0003g0187 |
3 | HG02717.hp1 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.833+1220C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280071 | |||||||
| chr10:114280130 | T | G | 18 | a0001c0001t0003g0171 a0001c0001t0003g0185 a0001c0001t0003g0187 others(15): Show |
18 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.833+1279T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280130 | |||||||
| chr10:114280242 | A | G | 76 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0123 others(73): Show |
76 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.833+1391A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280242 | |||||||
| chr10:114280327 | C | T | 2 | a0003c0020t0020g0039 a0005c0005t0004g0231 |
2 | HG02976.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.833+1476C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280327 | |||||||
| chr10:114280411 | G | A | 66 | a0001c0001t0001g0123 a0001c0001t0001g0154 a0001c0001t0001g0155 others(63): Show |
66 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.833+1560G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280411 | |||||||
| chr10:114280422 | G | A | 2 | a0002c0002t0001g0200 a0002c0002t0033g0220 |
2 | HG00738.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.833+1571G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280422 | |||||||
| chr10:114280425 | A | G | 30 | a0001c0001t0003g0066 a0001c0001t0003g0149 a0001c0001t0003g0171 others(27): Show |
30 | HG00735.hp1 HG00738.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.833+1574A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280425 | |||||||
| chr10:114280555 | C | G | 3 | a0001c0001t0007g0086 a0002c0002t0003g0109 a0014c0021t0020g0233 |
3 | HG01081.hp2 HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.833+1704C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280555 | |||||||
| chr10:114280609 | C | T | 2 | a0002c0002t0003g0071 a0025c0029t0023g0194 |
2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.833+1758C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280609 | |||||||
| chr10:114280674 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.833+1823C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280674 | |||||||
| chr10:114280706 | C | A | 1 | a0002c0002t0009g0229 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.834-1810C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280706 | |||||||
| chr10:114280856 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.834-1660A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280856 | |||||||
| chr10:114280893 | C | T | 1 | a0025c0029t0023g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.834-1623C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114280893 | |||||||
| chr10:114281014 | C | T | 121 | a0001c0001t0001g0102 a0001c0001t0001g0126 a0001c0001t0001g0133 others(118): Show |
121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.834-1502C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281014 | |||||||
| chr10:114281021 | T | C | 1 | a0002c0002t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.834-1495T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281021 | |||||||
| chr10:114281148 | G | C | 14 | a0001c0001t0002g0148 a0001c0001t0031g0144 a0002c0002t0001g0072 others(11): Show |
14 | HG00280.hp2 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.834-1368G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281148 | |||||||
| chr10:114281327 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.834-1189C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281327 | |||||||
| chr10:114281331 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.834-1185G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281331 | |||||||
| chr10:114281366 | G | A | 1 | a0002c0002t0002g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.834-1150G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281366 | |||||||
| chr10:114281428 | A | G | 1 | a0003c0023t0034g0005 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.834-1088A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281428 | |||||||
| chr10:114281478 | A | G | 5 | a0001c0001t0022g0099 a0001c0001t0022g0158 a0003c0003t0017g0013 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.834-1038A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281478 | |||||||
| chr10:114281518 | G | A | 134 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.834-998G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281518 | |||||||
| chr10:114281722 | C | A | 1 | a0003c0007t0024g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.834-794C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281722 | |||||||
| chr10:114281783 | A | G | 2 | a0002c0002t0001g0139 a0002c0002t0001g0140 |
2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.834-733A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281783 | |||||||
| chr10:114281930 | T | C | 3 | a0001c0001t0003g0149 a0012c0024t0003g0090 a0015c0018t0021g0043 |
3 | HG02559.hp1 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.834-586T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281930 | |||||||
| chr10:114281947 | C | T | 2 | a0002c0002t0003g0071 a0002c0002t0003g0109 |
2 | HG01081.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.834-569C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281947 | |||||||
| chr10:114281991 | C | A | 1 | a0001c0001t0023g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.834-525C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114281991 | |||||||
| chr10:114282012 | G | A | 4 | a0001c0001t0022g0099 a0001c0001t0022g0158 a0003c0003t0017g0013 others(1): Show |
4 | HG01884.hp1 HG02280.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.834-504G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114282012 | |||||||
| chr10:114282017 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0003g0149 a0001c0001t0031g0144 a0002c0002t0001g0094 others(5): Show |
8 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-489_834-488ins others(12): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 114282017 | ||||||
| chr10:114282017 | C | CTTTTTTT others(6): Show |
158 | a0001c0001t0001g0031 a0001c0001t0001g0102 a0001c0001t0001g0126 others(155): Show |
158 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.834-489_834-488ins others(13): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 114282017 | ||||||
| chr10:114282017 | C | CTTTTTTT others(7): Show |
10 | a0001c0001t0001g0030 a0001c0001t0003g0190 a0001c0001t0007g0086 others(7): Show |
10 | HG00609.hp1 HG01358.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.834-489_834-488ins others(14): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 114282017 | ||||||
| chr10:114282017 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0023g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.834-489_834-488ins others(17): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 114282017 | ||||||
| chr10:114282086 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.834-430C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114282086 | |||||||
| chr10:114282095 | T | C | 183 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(180): Show |
183 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.834-421T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114282095 | |||||||
| chr10:114282134 | G | A | 1 | a0017c0017t0027g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.834-382G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114282134 | |||||||
| chr10:114282235 | C | G | 7 | a0001c0001t0007g0069 a0001c0001t0007g0086 a0001c0001t0007g0100 others(4): Show |
7 | HG02257.hp1 HG02572.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.834-281C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114282235 | |||||||
| chr10:114282379 | A | G | 3 | a0001c0001t0002g0161 a0001c0001t0002g0167 a0002c0002t0002g0218 |
3 | HG01975.hp1 HG02300.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.834-137A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114282379 | |||||||
| chr10:114282384 | C | G | 2 | a0001c0001t0023g0165 a0025c0029t0023g0194 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.834-132C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114282384 | |||||||
| chr10:114282469 | C | T | 8 | a0001c0001t0003g0002 a0001c0001t0003g0106 a0001c0001t0003g0107 others(5): Show |
8 | HG00735.hp1 HG01081.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.834-47C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 8/13 | chr10 | 114282469 | |||||||
| chr10:114282708 | G | A | 2 | a0001c0001t0023g0165 a0025c0029t0023g0194 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.889+137G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114282708 | |||||||
| chr10:114282802 | G | A | 3 | a0001c0001t0003g0190 a0003c0003t0024g0003 a0003c0003t0038g0048 |
3 | HG02572.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.889+231G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114282802 | |||||||
| chr10:114282817 | G | A | 2 | a0001c0001t0023g0165 a0025c0029t0023g0194 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.889+246G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114282817 | |||||||
| chr10:114282818 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.889+247C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114282818 | |||||||
| chr10:114282914 | C | T | 2 | a0001c0001t0023g0165 a0025c0029t0023g0194 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.889+343C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114282914 | |||||||
| chr10:114283227 | C | A | 1 | a0002c0002t0001g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.889+656C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114283227 | |||||||
| chr10:114283252 | C | T | 3 | a0001c0001t0003g0066 a0001c0001t0003g0190 a0003c0003t0024g0003 |
3 | HG02258.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.889+681C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114283252 | |||||||
| chr10:114283286 | C | G | 1 | a0001c0001t0031g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.889+715C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114283286 | |||||||
| chr10:114283295 | C | CAGCGAGC others(21): Show |
2 | a0002c0002t0006g0093 a0004c0004t0004g0188 |
2 | HG01934.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.889+815_889+842dup others(28): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 114283295 | ||||||
| chr10:114283295 | CAGCGAGC others(21): Show |
C | 13 | a0001c0001t0001g0177 a0001c0001t0013g0084 a0001c0001t0013g0110 others(10): Show |
13 | HG00323.hp1 HG01109.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.889+815_889+842del others(28): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 114283295 | ||||||
| chr10:114283298 | C | T | 4 | a0001c0001t0003g0149 a0001c0001t0031g0144 a0012c0024t0003g0090 others(1): Show |
4 | HG02559.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.889+727C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114283298 | |||||||
| chr10:114283326 | C | T | 6 | a0001c0001t0013g0084 a0001c0001t0013g0110 a0001c0001t0013g0236 others(3): Show |
6 | HG00323.hp1 HG01109.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.889+755C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114283326 | |||||||
| chr10:114283363 | A | C | 2 | a0001c0001t0023g0165 a0025c0029t0023g0194 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.889+792A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114283363 | |||||||
| chr10:114283477 | C | T | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.889+906C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114283477 | |||||||
| chr10:114283585 | C | A | 2 | a0004c0004t0004g0147 a0005c0005t0004g0136 |
2 | HG00642.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.889+1014C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114283585 | |||||||
| chr10:114283667 | T | A | 36 | a0001c0001t0013g0119 a0004c0004t0001g0124 a0004c0004t0004g0065 others(33): Show |
36 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.889+1096T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114283667 | |||||||
| chr10:114284012 | A | T | 1 | a0002c0002t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.890-851A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114284012 | |||||||
| chr10:114284040 | C | G | 1 | a0002c0002t0001g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.890-823C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114284040 | |||||||
| chr10:114284090 | G | A | 1 | a0024c0030t0004g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.890-773G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114284090 | |||||||
| chr10:114284156 | C | G | 99 | a0001c0001t0001g0145 a0001c0001t0001g0166 a0001c0001t0002g0029 others(96): Show |
99 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.890-707C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114284156 | |||||||
| chr10:114284580 | C | T | 1 | a0001c0001t0003g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.890-283C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114284580 | |||||||
| chr10:114284605 | T | C | 215 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.890-258T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114284605 | |||||||
| chr10:114284760 | G | A | 2 | a0001c0001t0023g0165 a0025c0029t0023g0194 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.890-103G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114284760 | |||||||
| chr10:114284828 | C | T | 107 | a0001c0001t0001g0145 a0001c0001t0002g0029 a0001c0001t0002g0045 others(104): Show |
107 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.890-35C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 9/13 | chr10 | 114284828 | |||||||
| chr10:114285123 | G | A | 4 | a0001c0001t0003g0002 a0001c0001t0003g0106 a0001c0001t0003g0107 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+153G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285123 | |||||||
| chr10:114285192 | C | A | 42 | a0001c0001t0003g0066 a0001c0001t0003g0149 a0001c0001t0003g0190 others(39): Show |
42 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.997+222C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285192 | |||||||
| chr10:114285279 | G | T | 1 | a0001c0001t0002g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.997+309G>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285279 | |||||||
| chr10:114285332 | C | T | 1 | a0001c0001t0013g0084 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.997+362C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285332 | |||||||
| chr10:114285378 | T | C | 1 | a0002c0002t0002g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.997+408T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285378 | |||||||
| chr10:114285443 | C | T | 1 | a0002c0002t0002g0062 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.997+473C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285443 | |||||||
| chr10:114285559 | C | T | 3 | a0001c0001t0003g0066 a0001c0001t0003g0190 a0003c0003t0024g0003 |
3 | HG02258.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.998-380C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285559 | |||||||
| chr10:114285818 | T | C | 160 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.998-121T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285818 | |||||||
| chr10:114285818 | T | G | 1 | a0002c0002t0001g0228 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.998-121T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285818 | |||||||
| chr10:114285910 | G | A | 3 | a0001c0001t0003g0149 a0012c0024t0003g0090 a0015c0018t0021g0043 |
3 | HG02559.hp1 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.998-29G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285910 | |||||||
| chr10:114285935 | G | A | 1 | a0002c0002t0002g0087 | 1 | HG01175.hp2 | splice_region_variant&intron_variant | LOW | c.998-4G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 10/13 | chr10 | 114285935 | |||||||
| chr10:114286820 | G | A | 221 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1570+309G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114286820 | |||||||
| chr10:114286971 | C | T | 1 | a0001c0001t0023g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1570+460C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114286971 | |||||||
| chr10:114287004 | C | T | 3 | a0003c0003t0010g0047 a0003c0013t0012g0041 a0003c0013t0012g0157 |
3 | HG02630.hp2 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1570+493C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287004 | |||||||
| chr10:114287262 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1570+751C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287262 | |||||||
| chr10:114287281 | C | T | 63 | a0001c0001t0001g0145 a0001c0001t0002g0029 a0001c0001t0002g0045 others(60): Show |
63 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1570+770C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287281 | |||||||
| chr10:114287677 | G | C | 155 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1570+1166G>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287677 | |||||||
| chr10:114287689 | T | A | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1570+1178T>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287689 | |||||||
| chr10:114287694 | A | T | 7 | a0001c0001t0003g0066 a0001c0001t0003g0190 a0001c0001t0031g0144 others(4): Show |
7 | HG02258.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1570+1183A>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287694 | |||||||
| chr10:114287737 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1571-1201A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287737 | |||||||
| chr10:114287763 | C | T | 4 | a0003c0007t0014g0006 a0003c0007t0014g0007 a0003c0007t0014g0008 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571-1175C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287763 | |||||||
| chr10:114287773 | C | T | 1 | a0002c0002t0006g0092 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1571-1165C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287773 | |||||||
| chr10:114287799 | T | C | 1 | a0001c0035t0003g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1571-1139T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287799 | |||||||
| chr10:114287856 | C | T | 1 | a0001c0001t0013g0110 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1571-1082C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114287856 | |||||||
| chr10:114288162 | G | A | 64 | a0001c0001t0001g0145 a0001c0001t0001g0166 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1571-776G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288162 | |||||||
| chr10:114288232 | C | A | 1 | a0002c0002t0009g0229 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1571-706C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288232 | |||||||
| chr10:114288256 | T | C | 2 | a0001c0001t0023g0165 a0025c0029t0023g0194 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1571-682T>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288256 | |||||||
| chr10:114288286 | C | A | 12 | a0001c0001t0013g0084 a0001c0001t0013g0110 a0001c0001t0013g0236 others(9): Show |
12 | HG00323.hp1 HG00642.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1571-652C>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288286 | |||||||
| chr10:114288299 | G | A | 95 | a0001c0001t0001g0102 a0001c0001t0001g0123 a0001c0001t0001g0126 others(92): Show |
95 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1571-639G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288299 | |||||||
| chr10:114288361 | G | A | 1 | a0001c0001t0031g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1571-577G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288361 | |||||||
| chr10:114288444 | A | C | 50 | a0001c0001t0001g0145 a0001c0001t0001g0166 a0001c0001t0002g0029 others(47): Show |
50 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1571-494A>C | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288444 | |||||||
| chr10:114288475 | C | G | 2 | a0001c0001t0023g0165 a0025c0029t0023g0194 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1571-463C>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288475 | |||||||
| chr10:114288519 | A | G | 2 | a0004c0004t0004g0238 a0018c0022t0015g0054 |
2 | HG00438.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1571-419A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288519 | |||||||
| chr10:114288543 | G | A | 64 | a0001c0001t0001g0145 a0001c0001t0001g0166 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1571-395G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288543 | |||||||
| chr10:114288549 | G | A | 64 | a0001c0001t0001g0145 a0001c0001t0001g0166 a0001c0001t0002g0029 others(61): Show |
64 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1571-389G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288549 | |||||||
| chr10:114288804 | A | G | 3 | a0001c0001t0022g0099 a0001c0001t0022g0158 a0019c0015t0028g0042 |
3 | HG01884.hp1 HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1571-134A>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288804 | |||||||
| chr10:114288847 | T | G | 1 | a0003c0016t0003g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1571-91T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 11/13 | chr10 | 114288847 | |||||||
| chr10:114289538 | C | T | 2 | a0001c0001t0001g0169 a0003c0003t0012g0026 |
2 | HG01081.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2122+49C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/13 | chr10 | 114289538 | |||||||
| chr10:114289948 | C | T | 101 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(98): Show |
101 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.2123-292C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/13 | chr10 | 114289948 | |||||||
| chr10:114289992 | CA | C | 136 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(133): Show |
136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.2123-230delA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 114289992 | ||||||
| chr10:114289992 | CAA | C | 60 | a0001c0001t0002g0029 a0001c0001t0002g0045 a0001c0001t0002g0063 others(57): Show |
60 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.2123-231_2123-230d others(4): Show |
VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 114289992 | ||||||
| chr10:114290187 | C | T | 15 | a0001c0001t0022g0099 a0001c0001t0022g0158 a0002c0010t0005g0073 others(12): Show |
15 | HG01884.hp1 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2123-53C>T | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 12/13 | chr10 | 114290187 | |||||||
| chr10:114290370 | G | A | 1 | a0003c0003t0011g0015 | 1 | HG03834.hp1 | splice_region_variant&intron_variant | LOW | c.2248+5G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 13/13 | chr10 | 114290370 | |||||||
| chr10:114290413 | G | A | 1 | a0003c0019t0021g0024 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2248+48G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 13/13 | chr10 | 114290413 | |||||||
| chr10:114290572 | T | G | 1 | a0017c0017t0027g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2248+207T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 13/13 | chr10 | 114290572 | |||||||
| chr10:114290669 | G | A | 1 | a0017c0017t0027g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2248+304G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 13/13 | chr10 | 114290669 | |||||||
| chr10:114290722 | CA | C | 61 | a0001c0001t0002g0029 a0001c0001t0002g0045 a0001c0001t0002g0063 others(58): Show |
61 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2248+358delA | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 13/13 | chr10 | 114290722 | |||||||
| chr10:114290887 | G | A | 1 | a0014c0021t0020g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2249-331G>A | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 13/13 | chr10 | 114290887 | |||||||
| chr10:114290895 | T | G | 1 | a0002c0002t0001g0210 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2249-323T>G | VWA2 | ENSG00000165816.13 | transcript | ENST00000392982.8 | protein_coding | 13/13 | chr10 | 114290895 |