Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8876 |
| ensemblid | ENSG00000112299.8 |
| hgncid | 12705 |
| symbol | VNN1 |
| name | vanin 1 |
| refseq_nuc | NM_004666.3 |
| refseq_prot | NP_004657.2 |
| ensembl_nuc | ENST00000367928.5 |
| ensembl_prot | ENSP00000356905.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 132680849 |
| end | 132714055 |
| strand | - |
| ver | v1.2 |
| region | chr6:132680849-132714055 |
| region5000 | chr6:132675849-132719055 |
| regionname0 | VNN1_chr6_132680849_132714055 |
| regionname5000 | VNN1_chr6_132675849_132719055 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 513 | 175 | 44 | 31 | 78 | 2 | 20 | 63 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0002 | 1/1 | 513 | 105 | 6 | 29 | 49 | 9 | 10 | 34 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0003 | 0/0 | 513 | 83 | 1 | 21 | 51 | 4 | 6 | 40 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0004 | 0/0 | 513 | 22 | 15 | 1 | 1 | 1 | 4 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0005 | 0/0 | 513 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0006 | 0/0 | 513 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0007 | 0/0 | 513 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0008 | 0/0 | 513 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0009 | 0/0 | 513 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0010 | 0/0 | 513 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0011 | 0/0 | 513 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0012 | 0/0 | 513 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0013 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0014 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0015 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0016 | 0/0 | 513 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0017 | 0/0 | 513 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| a0018 | 0/0 | 513 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | MTTQL others(508): Show |
chr6 | 132675849 | 132719055 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1539 | 174 | 44 | 31 | 78 | 2 | 19 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0001c0020 | 0/0 | 1539 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0002c0002 | 1/1 | 1539 | 104 | 5 | 29 | 49 | 9 | 10 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0002c0013 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0003c0003 | 0/0 | 1539 | 82 | 1 | 21 | 50 | 4 | 6 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0003c0012 | 0/0 | 1539 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0004c0004 | 0/0 | 1539 | 22 | 15 | 1 | 1 | 1 | 4 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0005c0005 | 0/0 | 1539 | 7 | 7 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0005c0008 | 0/0 | 1539 | 3 | 3 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0006c0006 | 0/0 | 1539 | 3 | 3 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0006c0017 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0007c0011 | 0/0 | 1539 | 2 | 0 | 2 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0007c0022 | 0/0 | 1539 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0008c0007 | 0/0 | 1539 | 3 | 3 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0009c0009 | 0/0 | 1539 | 3 | 0 | 0 | 3 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0010c0010 | 0/0 | 1539 | 2 | 0 | 1 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0011c0016 | 0/0 | 1539 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0012c0014 | 0/0 | 1539 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0013c0015 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0014c0021 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0015c0018 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0016c0019 | 0/0 | 1539 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0017c0023 | 0/0 | 1539 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 | ||
| a0018c0024 | 0/0 | 1539 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | ATGAC others(1534): Show |
chr6 | 132675849 | 132719055 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3853 | 115 | 33 | 12 | 59 | 0 | 11 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0002 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0003 | 0/0 | 3853 | 33 | 0 | 13 | 16 | 1 | 3 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0004 | 0/0 | 3853 | 2 | 2 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0005 | 0/0 | 3853 | 7 | 1 | 2 | 0 | 1 | 3 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0007 | 0/0 | 3853 | 5 | 0 | 3 | 1 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0009 | 0/0 | 3853 | 5 | 5 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0019 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0026 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0027 | 0/0 | 3853 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0028 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0029 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0001t0030 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0001c0020t0001 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0002t0001 | 0/0 | 3853 | 9 | 0 | 0 | 9 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0002t0002 | 0/0 | 3853 | 23 | 1 | 11 | 4 | 4 | 3 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0002t0003 | 1/1 | 3853 | 37 | 3 | 14 | 10 | 2 | 6 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0002t0004 | 0/0 | 3853 | 26 | 0 | 1 | 22 | 2 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0002t0005 | 0/0 | 3853 | 4 | 0 | 3 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0002t0015 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0002t0016 | 0/0 | 3853 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0002t0024 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0002t0035 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0002c0013t0003 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0003c0003t0002 | 0/0 | 3853 | 68 | 1 | 16 | 48 | 1 | 2 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0003c0003t0003 | 0/0 | 3853 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0003c0003t0006 | 0/0 | 3853 | 5 | 0 | 0 | 0 | 1 | 4 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0003c0003t0012 | 0/0 | 3853 | 4 | 0 | 3 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0003c0003t0018 | 0/0 | 3853 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0003c0003t0031 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0003c0003t0032 | 0/0 | 3853 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0003c0012t0002 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0004c0004t0001 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0004c0004t0003 | 0/0 | 3853 | 11 | 7 | 0 | 1 | 0 | 3 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0004c0004t0006 | 0/0 | 3853 | 3 | 0 | 1 | 0 | 1 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0004c0004t0007 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0004c0004t0013 | 0/0 | 3853 | 2 | 2 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0004c0004t0014 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0004c0004t0017 | 0/0 | 3853 | 2 | 2 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0004c0004t0034 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0005c0005t0010 | 0/0 | 3855 | 3 | 3 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3850): Show |
chr6 | 132675849 | 132719055 |
| a0005c0005t0014 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0005c0005t0020 | 0/0 | 3855 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3850): Show |
chr6 | 132675849 | 132719055 |
| a0005c0005t0022 | 0/0 | 3855 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3850): Show |
chr6 | 132675849 | 132719055 |
| a0005c0005t0023 | 0/0 | 3855 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3850): Show |
chr6 | 132675849 | 132719055 |
| a0005c0008t0008 | 0/0 | 3855 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3850): Show |
chr6 | 132675849 | 132719055 |
| a0005c0008t0010 | 0/0 | 3855 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3850): Show |
chr6 | 132675849 | 132719055 |
| a0005c0008t0021 | 0/0 | 3855 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3850): Show |
chr6 | 132675849 | 132719055 |
| a0006c0006t0011 | 0/0 | 3853 | 3 | 3 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0006c0017t0011 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0007c0011t0005 | 0/0 | 3853 | 2 | 0 | 2 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0007c0022t0005 | 0/0 | 3853 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0008c0007t0008 | 0/0 | 3855 | 3 | 3 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3850): Show |
chr6 | 132675849 | 132719055 |
| a0009c0009t0003 | 0/0 | 3853 | 3 | 0 | 0 | 3 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0010c0010t0001 | 0/0 | 3853 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0010c0010t0003 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0011c0016t0001 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0012c0014t0033 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0013c0015t0025 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0014c0021t0015 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0015c0018t0008 | 0/0 | 3855 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3850): Show |
chr6 | 132675849 | 132719055 |
| a0016c0019t0001 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0017c0023t0003 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| a0018c0024t0003 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | AGCAC others(3848): Show |
chr6 | 132675849 | 132719055 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 27 | 5 | 5 | 14 | 0 | 3 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0006 | 0/0 | 12 | 0 | 2 | 9 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0003 | 0/0 | 13 | 0 | 3 | 7 | 1 | 2 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0015 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0005g0027 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0005g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0007g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0009g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0019g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0026g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0027g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0028g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0029g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0001t0030g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0001c0020t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0002g0007 | 0/0 | 11 | 0 | 7 | 0 | 2 | 2 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0005 | 1/0 | 12 | 0 | 4 | 4 | 1 | 2 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0009 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0022 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0023 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0004 | 0/0 | 12 | 0 | 0 | 11 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0005g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0015g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0016g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0016g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0024g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0002t0035g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0002c0013t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0001 | 0/0 | 43 | 0 | 4 | 36 | 1 | 2 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0006g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0006g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0012g0014 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0018g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0031g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0003t0032g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0003c0012t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0006g0028 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0013g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0014g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0017g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0017g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0004c0004t0034g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0005c0005t0010g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0005c0005t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0005c0005t0014g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0005c0005t0020g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0005c0005t0022g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0005c0005t0023g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0005c0008t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0005c0008t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0005c0008t0021g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0006c0006t0011g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0006c0017t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0007c0011t0005g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0007c0022t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0008c0007t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0008c0007t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0008c0007t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0009c0009t0003g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0009c0009t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0010c0010t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0010c0010t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0011c0016t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0012c0014t0033g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0013c0015t0025g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0014c0021t0015g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0015c0018t0008g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0016c0019t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0017c0023t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| a0018c0024t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0182 | EUR | GBR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0007 | EUR | GBR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0109 | EUR | GBR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00140 | hp2 | a0002 | c0002 | t0004 | g0004 | EUR | GBR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0100 | EUR | FIN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00280 | hp2 | a0004 | c0004 | t0006 | g0028 | EUR | FIN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00323 | hp1 | a0003 | c0003 | t0031 | g0084 | EUR | FIN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00323 | hp2 | a0003 | c0003 | t0006 | g0037 | EUR | FIN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00408 | hp2 | a0011 | c0016 | t0001 | g0065 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00544 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00558 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00597 | hp1 | a0003 | c0003 | t0002 | g0090 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00609 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00609 | hp2 | a0003 | c0003 | t0002 | g0088 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0022 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00639 | hp2 | a0004 | c0004 | t0006 | g0028 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00673 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0009 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00733 | hp2 | a0003 | c0003 | t0012 | g0014 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00735 | hp2 | a0007 | c0011 | t0005 | g0051 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00738 | hp1 | a0002 | c0002 | t0005 | g0020 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0022 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00741 | hp1 | a0002 | c0002 | t0003 | g0034 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG00741 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01069 | hp1 | a0003 | c0003 | t0002 | g0012 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01070 | hp1 | a0002 | c0002 | t0005 | g0020 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01070 | hp2 | a0003 | c0003 | t0003 | g0080 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01071 | hp1 | a0002 | c0002 | t0005 | g0020 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0012 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01074 | hp1 | a0007 | c0011 | t0005 | g0051 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01081 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01106 | hp1 | a0007 | c0022 | t0005 | g0184 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01109 | hp1 | a0002 | c0002 | t0003 | g0102 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01109 | hp2 | a0002 | c0002 | t0004 | g0106 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0012 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01169 | hp2 | a0003 | c0003 | t0002 | g0012 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01175 | hp2 | a0002 | c0002 | t0003 | g0034 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01192 | hp1 | a0003 | c0003 | t0032 | g0085 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01192 | hp2 | a0010 | c0010 | t0001 | g0116 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01243 | hp2 | a0003 | c0003 | t0002 | g0086 | AMR | PUR | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01256 | hp2 | a0003 | c0003 | t0012 | g0014 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01257 | hp2 | a0002 | c0002 | t0003 | g0009 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01258 | hp1 | a0002 | c0002 | t0003 | g0009 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01258 | hp2 | a0003 | c0003 | t0012 | g0014 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0038 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01346 | hp2 | a0002 | c0002 | t0003 | g0056 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0009 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0044 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01361 | hp2 | a0003 | c0003 | t0002 | g0089 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01433 | hp1 | a0003 | c0003 | t0002 | g0067 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01515 | hp1 | a0002 | c0002 | t0005 | g0063 | EUR | IBS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01515 | hp2 | a0003 | c0003 | t0012 | g0014 | EUR | IBS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01516 | hp1 | a0002 | c0002 | t0003 | g0005 | EUR | IBS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01516 | hp2 | a0003 | c0003 | t0002 | g0001 | EUR | IBS | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0148 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01943 | hp1 | a0003 | c0003 | t0002 | g0058 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01952 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01975 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0091 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0111 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01981 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01993 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01993 | hp2 | a0001 | c0001 | t0027 | g0155 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0052 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02055 | hp1 | a0006 | c0006 | t0011 | g0024 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02055 | hp2 | a0005 | c0008 | t0010 | g0207 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02056 | hp1 | a0002 | c0002 | t0003 | g0104 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02056 | hp2 | a0003 | c0003 | t0002 | g0057 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02071 | hp1 | a0002 | c0002 | t0016 | g0070 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02074 | hp1 | a0002 | c0002 | t0003 | g0095 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02074 | hp2 | a0002 | c0002 | t0003 | g0103 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02080 | hp1 | a0003 | c0003 | t0002 | g0093 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02083 | hp1 | a0002 | c0002 | t0004 | g0033 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0199 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0087 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02145 | hp1 | a0005 | c0005 | t0010 | g0123 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02148 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02273 | hp1 | a0003 | c0003 | t0002 | g0019 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02273 | hp2 | a0001 | c0001 | t0007 | g0044 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02280 | hp1 | a0004 | c0004 | t0013 | g0043 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02293 | hp2 | a0003 | c0003 | t0002 | g0059 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0082 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PEL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02523 | hp2 | a0002 | c0002 | t0024 | g0075 | EAS | KHV | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02602 | hp1 | a0004 | c0004 | t0003 | g0134 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02630 | hp1 | a0004 | c0004 | t0013 | g0043 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02630 | hp2 | a0004 | c0004 | t0003 | g0129 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02683 | hp1 | a0003 | c0003 | t0002 | g0001 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0177 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02698 | hp2 | a0004 | c0004 | t0006 | g0028 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02717 | hp1 | a0004 | c0004 | t0034 | g0149 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02723 | hp1 | a0004 | c0004 | t0003 | g0130 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02723 | hp2 | a0008 | c0007 | t0008 | g0119 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02735 | hp1 | a0012 | c0014 | t0033 | g0094 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0027 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02809 | hp1 | a0004 | c0004 | t0003 | g0127 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02818 | hp2 | a0005 | c0005 | t0010 | g0039 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02886 | hp1 | a0006 | c0006 | t0011 | g0024 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02886 | hp2 | a0013 | c0015 | t0025 | g0115 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02922 | hp1 | a0001 | c0001 | t0019 | g0054 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02922 | hp2 | a0004 | c0004 | t0001 | g0137 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02965 | hp2 | a0004 | c0004 | t0003 | g0040 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0113 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03098 | hp1 | a0005 | c0005 | t0014 | g0121 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0083 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03139 | hp1 | a0014 | c0021 | t0015 | g0185 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03195 | hp2 | a0005 | c0005 | t0010 | g0039 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03225 | hp1 | a0008 | c0007 | t0008 | g0118 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03239 | hp1 | a0001 | c0020 | t0001 | g0179 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03453 | hp2 | a0004 | c0004 | t0003 | g0132 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03486 | hp1 | a0005 | c0005 | t0020 | g0122 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03491 | hp2 | a0003 | c0003 | t0006 | g0035 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03492 | hp2 | a0003 | c0003 | t0006 | g0035 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03516 | hp2 | a0002 | c0002 | t0015 | g0112 | AFR | ESN | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03540 | hp2 | a0015 | c0018 | t0008 | g0124 | AFR | GWD | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03579 | hp1 | a0006 | c0006 | t0011 | g0024 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03654 | hp1 | a0003 | c0003 | t0006 | g0062 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03654 | hp2 | a0003 | c0003 | t0006 | g0037 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0023 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0023 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03710 | hp1 | a0002 | c0002 | t0003 | g0009 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0145 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03834 | hp1 | a0001 | c0001 | t0029 | g0180 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03834 | hp2 | a0002 | c0002 | t0004 | g0068 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03927 | hp2 | a0016 | c0019 | t0001 | g0192 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03942 | hp1 | a0002 | c0002 | t0003 | g0097 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0052 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04115 | hp1 | a0004 | c0004 | t0003 | g0135 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04184 | hp1 | a0017 | c0023 | t0003 | g0147 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04184 | hp2 | a0010 | c0010 | t0003 | g0139 | SAS | BEB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0005 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0108 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04204 | hp2 | a0003 | c0003 | t0002 | g0001 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04228 | hp1 | a0004 | c0004 | t0003 | g0133 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0174 | SAS | STU | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18522 | hp2 | a0004 | c0004 | t0007 | g0154 | AFR | YRI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | CHB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18747 | hp1 | a0003 | c0003 | t0018 | g0029 | EAS | CHB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18747 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | CHB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18906 | hp1 | a0008 | c0007 | t0008 | g0120 | AFR | YRI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18906 | hp2 | a0001 | c0001 | t0028 | g0178 | AFR | YRI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18942 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18944 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18948 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18950 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18953 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18953 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18956 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18957 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18957 | hp2 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18960 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18962 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18964 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18965 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18966 | hp2 | a0002 | c0002 | t0016 | g0079 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18969 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18969 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18972 | hp1 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18972 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18975 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18977 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18979 | hp2 | a0009 | c0009 | t0003 | g0210 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18980 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18981 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18982 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18983 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18985 | hp1 | a0003 | c0003 | t0002 | g0060 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18985 | hp2 | a0002 | c0002 | t0004 | g0078 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18988 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18990 | hp2 | a0001 | c0001 | t0026 | g0198 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18992 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18995 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18997 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18997 | hp2 | a0004 | c0004 | t0003 | g0131 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18998 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19000 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19002 | hp1 | a0002 | c0002 | t0004 | g0076 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19003 | hp1 | a0002 | c0002 | t0004 | g0071 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19003 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19004 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19005 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19005 | hp2 | a0003 | c0012 | t0002 | g0055 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19006 | hp1 | a0003 | c0003 | t0018 | g0029 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19007 | hp2 | a0002 | c0002 | t0004 | g0032 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19009 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19011 | hp2 | a0009 | c0009 | t0003 | g0053 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19012 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19012 | hp2 | a0002 | c0002 | t0003 | g0098 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0101 | AFR | LWK | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19043 | hp1 | a0002 | c0013 | t0003 | g0061 | AFR | LWK | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19054 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19055 | hp2 | a0002 | c0002 | t0004 | g0073 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19056 | hp1 | a0002 | c0002 | t0035 | g0107 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19058 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19062 | hp1 | a0002 | c0002 | t0004 | g0032 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19063 | hp1 | a0002 | c0002 | t0003 | g0114 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19064 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19064 | hp2 | a0002 | c0002 | t0004 | g0074 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19065 | hp1 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19068 | hp1 | a0001 | c0001 | t0030 | g0163 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19068 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19078 | hp1 | a0003 | c0003 | t0002 | g0081 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19079 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19080 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19081 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0077 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19082 | hp1 | a0009 | c0009 | t0003 | g0053 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19082 | hp2 | a0002 | c0002 | t0004 | g0033 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19088 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19088 | hp2 | a0002 | c0002 | t0004 | g0069 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19090 | hp1 | a0018 | c0024 | t0003 | g0211 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19240 | hp1 | a0005 | c0008 | t0008 | g0206 | AFR | YRI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA19240 | hp2 | a0004 | c0004 | t0003 | g0040 | AFR | YRI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20129 | hp2 | a0002 | c0002 | t0003 | g0023 | AFR | ASW | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0007 | EUR | TSI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20752 | hp2 | a0002 | c0002 | t0004 | g0072 | EUR | TSI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0099 | EUR | TSI | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | GIH | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0005 | SAS | GIH | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0022 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02486 | hp2 | a0004 | c0004 | t0003 | g0126 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02559 | hp1 | a0004 | c0004 | t0017 | g0161 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03471 | hp1 | a0005 | c0008 | t0021 | g0202 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| HG06807 | hp2 | a0004 | c0004 | t0014 | g0128 | AFR | USA | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20300 | hp1 | a0006 | c0017 | t0011 | g0136 | AFR | USA | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA20300 | hp2 | a0005 | c0005 | t0023 | g0168 | AFR | USA | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA21309 | hp1 | a0004 | c0004 | t0017 | g0150 | AFR | LWK | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| NA21309 | hp2 | a0005 | c0005 | t0022 | g0125 | AFR | LWK | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0096 | REF | REF | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0003 | g0005 | REF | REF | VNN1_chr6_132675849_132719055 | VNN1 | chr6 | 132675849 | 132719055 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:132683142 | A | G | 3 | a0005 a0008 a0015 |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
stop_lost | HIGH | c.1540T>C | p.Ter514Glnext*? | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1560/3853 | 1540/1542 | 514/513 | chr6 | 132683142 | |||
| chr6:132683295 | G | C | 1 | a0014 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.1387C>G | p.Leu463Val | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1407/3853 | 1387/1542 | 463/513 | chr6 | 132683295 | |||
| chr6:132692293 | A | G | 2 | a0008 a0015 |
4 | HG02723.hp2 HG03225.hp1 HG03540.hp2 others(1): Show |
missense_variant | MODERATE | c.1118T>C | p.Ile373Thr | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/7 | 1138/3853 | 1118/1542 | 373/513 | chr6 | 132692293 | |||
| chr6:132692393 | C | T | 1 | a0016 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.1018G>A | p.Asp340Asn | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/7 | 1038/3853 | 1018/1542 | 340/513 | chr6 | 132692393 | |||
| chr6:132692405 | T | C | 1 | a0007 | 3 | HG00735.hp2 HG01074.hp1 HG01106.hp1 |
missense_variant | MODERATE | c.1006A>G | p.Thr336Ala | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/7 | 1026/3853 | 1006/1542 | 336/513 | chr6 | 132692405 | |||
| chr6:132692437 | G | T | 2 | a0005 a0015 |
11 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(8): Show |
missense_variant | MODERATE | c.974C>A | p.Ala325Glu | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/7 | 994/3853 | 974/1542 | 325/513 | chr6 | 132692437 | |||
| chr6:132692523 | C | G | 1 | a0006 | 4 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.888G>C | p.Glu296Asp | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/7 | 908/3853 | 888/1542 | 296/513 | chr6 | 132692523 | |||
| chr6:132694054 | C | T | 1 | a0010 | 2 | HG01192.hp2 HG04184.hp2 |
missense_variant | MODERATE | c.470G>A | p.Arg157His | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/7 | 490/3853 | 470/1542 | 157/513 | chr6 | 132694054 | |||
| chr6:132694088 | C | T | 1 | a0011 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.436G>A | p.Asp146Asn | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/7 | 456/3853 | 436/1542 | 146/513 | chr6 | 132694088 | |||
| chr6:132694132 | T | C | 2 | a0003 a0004 |
105 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
missense_variant | MODERATE | c.392A>G | p.Asn131Ser | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/7 | 412/3853 | 392/1542 | 131/513 | chr6 | 132694132 | |||
| chr6:132711743 | C | T | 1 | a0013 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.307G>A | p.Glu103Lys | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/7 | 327/3853 | 307/1542 | 103/513 | chr6 | 132711743 | |||
| chr6:132711809 | C | T | 1 | a0012 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.241G>A | p.Ala81Thr | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/7 | 261/3853 | 241/1542 | 81/513 | chr6 | 132711809 | |||
| chr6:132711835 | G | A | 1 | a0017 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.215C>T | p.Ala72Val | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/7 | 235/3853 | 215/1542 | 72/513 | chr6 | 132711835 | |||
| chr6:132713873 | G | A | 1 | a0009 | 3 | NA18979.hp2 NA19011.hp2 NA19082.hp1 |
missense_variant | MODERATE | c.163C>T | p.Arg55Trp | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/7 | 183/3853 | 163/1542 | 55/513 | chr6 | 132713873 | |||
| chr6:132713923 | T | C | 1 | a0018 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.113A>G | p.Asn38Ser | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/7 | 133/3853 | 113/1542 | 38/513 | chr6 | 132713923 | |||
| chr6:132713959 | G | A | 13 | a0001 a0004 a0005 others(10): Show |
227 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(224): Show |
missense_variant | MODERATE | c.77C>T | p.Thr26Ile | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/7 | 97/3853 | 77/1542 | 26/513 | chr6 | 132713959 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:132683272 | G | T | 1 | a0001c0020 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.1410C>A | p.Val470Val | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1430/3853 | 1410/1542 | 470/513 | chr6 | 132683272 | |||
| chr6:132692394 | G | A | 1 | a0006c0017 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1017C>T | p.Phe339Phe | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/7 | 1037/3853 | 1017/1542 | 339/513 | chr6 | 132692394 | |||
| chr6:132693274 | C | T | 1 | a0007c0011 | 2 | HG00735.hp2 HG01074.hp1 |
synonymous_variant | LOW | c.576G>A | p.Lys192Lys | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 4/7 | 596/3853 | 576/1542 | 192/513 | chr6 | 132693274 | |||
| chr6:132694113 | T | A | 6 | a0002c0013 a0005c0005 a0006c0006 others(3): Show |
16 | HG02055.hp1 HG02145.hp1 HG02723.hp2 others(13): Show |
synonymous_variant | LOW | c.411A>T | p.Ala137Ala | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/7 | 431/3853 | 411/1542 | 137/513 | chr6 | 132694113 | |||
| chr6:132694119 | A | G | 6 | a0002c0013 a0005c0005 a0006c0006 others(3): Show |
16 | HG02055.hp1 HG02145.hp1 HG02723.hp2 others(13): Show |
synonymous_variant | LOW | c.405T>C | p.Val135Val | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/7 | 425/3853 | 405/1542 | 135/513 | chr6 | 132694119 | |||
| chr6:132711834 | C | T | 3 | a0002c0013 a0006c0006 a0006c0017 |
5 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(2): Show |
synonymous_variant | LOW | c.216G>A | p.Ala72Ala | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/7 | 236/3853 | 216/1542 | 72/513 | chr6 | 132711834 | |||
| chr6:132713889 | A | C | 1 | a0003c0012 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.147T>G | p.Ala49Ala | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/7 | 167/3853 | 147/1542 | 49/513 | chr6 | 132713889 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:132680929 | G | A | 14 | a0001c0001t0004 a0001c0001t0007 a0002c0002t0004 others(11): Show |
48 | HG00140.hp2 HG00609.hp1 HG01109.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2211C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 2211 | chr6 | 132680929 | ||||||
| chr6:132680989 | T | C | 1 | a0005c0008t0021 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2151A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 2151 | chr6 | 132680989 | ||||||
| chr6:132681043 | A | G | 6 | a0001c0001t0028 a0004c0004t0013 a0005c0005t0010 others(3): Show |
9 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2097T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 2097 | chr6 | 132681043 | ||||||
| chr6:132681130 | G | A | 14 | a0001c0001t0002 a0001c0001t0009 a0002c0002t0002 others(11): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2010C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 2010 | chr6 | 132681130 | ||||||
| chr6:132681218 | C | T | 2 | a0004c0004t0014 a0005c0005t0014 |
2 | HG03098.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1922G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1922 | chr6 | 132681218 | ||||||
| chr6:132681304 | A | C | 8 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(5): Show |
12 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1836T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1836 | chr6 | 132681304 | ||||||
| chr6:132681325 | G | A | 9 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(6): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1815C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1815 | chr6 | 132681325 | ||||||
| chr6:132681366 | C | T | 4 | a0001c0001t0005 a0002c0002t0005 a0007c0011t0005 others(1): Show |
14 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1774G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1774 | chr6 | 132681366 | ||||||
| chr6:132681383 | G | T | 9 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(6): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1757C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1757 | chr6 | 132681383 | ||||||
| chr6:132681464 | C | A | 8 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(5): Show |
12 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1676G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1676 | chr6 | 132681464 | ||||||
| chr6:132681649 | T | G | 1 | a0005c0008t0021 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1491A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1491 | chr6 | 132681649 | ||||||
| chr6:132681669 | A | C | 1 | a0003c0003t0032 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1471T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1471 | chr6 | 132681669 | ||||||
| chr6:132681826 | G | A | 1 | a0003c0003t0031 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1314 | chr6 | 132681826 | ||||||
| chr6:132681848 | G | A | 1 | a0001c0001t0029 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1292 | chr6 | 132681848 | ||||||
| chr6:132681951 | A | G | 9 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(6): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1189T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1189 | chr6 | 132681951 | ||||||
| chr6:132682095 | C | T | 9 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(6): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1045G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1045 | chr6 | 132682095 | ||||||
| chr6:132682103 | T | C | 4 | a0003c0003t0006 a0003c0003t0012 a0003c0003t0032 others(1): Show |
13 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1037A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1037 | chr6 | 132682103 | ||||||
| chr6:132682109 | A | T | 1 | a0001c0001t0027 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1031T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1031 | chr6 | 132682109 | ||||||
| chr6:132682112 | T | C | 9 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(6): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1028A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1028 | chr6 | 132682112 | ||||||
| chr6:132682134 | C | T | 1 | a0001c0001t0026 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1006G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 1006 | chr6 | 132682134 | ||||||
| chr6:132682191 | T | C | 1 | a0002c0002t0016 | 2 | HG02071.hp1 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*949A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 949 | chr6 | 132682191 | ||||||
| chr6:132682205 | C | T | 22 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(19): Show |
163 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*935G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 935 | chr6 | 132682205 | ||||||
| chr6:132682237 | G | C | 1 | a0005c0008t0021 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 903 | chr6 | 132682237 | ||||||
| chr6:132682395 | T | A | 1 | a0001c0001t0030 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*745A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 745 | chr6 | 132682395 | ||||||
| chr6:132682539 | C | T | 1 | a0013c0015t0025 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*601G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 601 | chr6 | 132682539 | ||||||
| chr6:132682554 | T | C | 1 | a0012c0014t0033 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*586A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 586 | chr6 | 132682554 | ||||||
| chr6:132682566 | C | G | 1 | a0003c0003t0012 | 4 | HG00733.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*574G>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 574 | chr6 | 132682566 | ||||||
| chr6:132682658 | A | G | 1 | a0005c0008t0021 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 482 | chr6 | 132682658 | ||||||
| chr6:132682726 | A | T | 31 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(28): Show |
176 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*414T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 414 | chr6 | 132682726 | ||||||
| chr6:132682746 | G | A | 9 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(6): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*394C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 394 | chr6 | 132682746 | ||||||
| chr6:132682783 | C | T | 2 | a0006c0006t0011 a0006c0017t0011 |
4 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*357G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 357 | chr6 | 132682783 | ||||||
| chr6:132682790 | T | A | 2 | a0004c0004t0017 a0004c0004t0034 |
3 | HG02559.hp1 HG02717.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*350A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 350 | chr6 | 132682790 | ||||||
| chr6:132682817 | C | T | 9 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(6): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*323G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 323 | chr6 | 132682817 | ||||||
| chr6:132682844 | T | TTA | 9 | a0005c0005t0010 a0005c0005t0020 a0005c0005t0022 others(6): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*294_*295dupTA | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 295 | chr6 | 132682844 | ||||||
| chr6:132682878 | C | T | 2 | a0002c0002t0024 a0005c0005t0020 |
2 | HG02523.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*262G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 262 | chr6 | 132682878 | ||||||
| chr6:132682890 | G | A | 1 | a0002c0002t0035 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*250C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 250 | chr6 | 132682890 | ||||||
| chr6:132682935 | T | C | 1 | a0003c0003t0018 | 2 | NA18747.hp1 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*205A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 7/7 | 205 | chr6 | 132682935 | ||||||
| chr6:132714047 | A | G | 1 | a0001c0001t0019 | 1 | HG02922.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-12T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/7 | chr6 | 132714047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:132683421 | A | G | 1 | a0002c0002t0003g0105 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1360-99T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683421 | |||||||
| chr6:132683524 | G | A | 12 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0020g0122 others(9): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1360-202C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683524 | |||||||
| chr6:132683564 | G | A | 12 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0020g0122 others(9): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1360-242C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683564 | |||||||
| chr6:132683633 | A | G | 1 | a0004c0004t0017g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1360-311T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683633 | |||||||
| chr6:132683662 | C | A | 9 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0020g0122 others(6): Show |
10 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1360-340G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683662 | |||||||
| chr6:132683750 | C | T | 1 | a0002c0002t0004g0074 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1360-428G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683750 | |||||||
| chr6:132683810 | C | T | 4 | a0008c0007t0008g0118 a0008c0007t0008g0119 a0008c0007t0008g0120 others(1): Show |
4 | HG02723.hp2 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1360-488G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683810 | |||||||
| chr6:132683837 | T | C | 12 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0020g0122 others(9): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1359+498A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683837 | |||||||
| chr6:132683852 | T | A | 29 | a0003c0003t0002g0001 a0003c0003t0002g0012 a0003c0003t0002g0019 others(26): Show |
85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1359+483A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683852 | |||||||
| chr6:132683887 | T | C | 12 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0020g0122 others(9): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1359+448A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683887 | |||||||
| chr6:132683976 | G | A | 1 | a0004c0004t0003g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1359+359C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132683976 | |||||||
| chr6:132684020 | G | A | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1359+315C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684020 | |||||||
| chr6:132684099 | C | T | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1359+236G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684099 | |||||||
| chr6:132684122 | A | T | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1359+213T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684122 | |||||||
| chr6:132684204 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1359+131A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684204 | |||||||
| chr6:132684205 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1359+130C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684205 | |||||||
| chr6:132684208 | C | A | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1359+127G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684208 | |||||||
| chr6:132684210 | C | A | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1359+125G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684210 | |||||||
| chr6:132684211 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1359+124G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684211 | |||||||
| chr6:132684213 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1359+122T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684213 | |||||||
| chr6:132684214 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1359+121C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684214 | |||||||
| chr6:132684218 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1359+117T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 6/6 | chr6 | 132684218 | |||||||
| chr6:132684584 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1189-79C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684584 | |||||||
| chr6:132684678 | T | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(80): Show |
163 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1189-173A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684678 | |||||||
| chr6:132684714 | A | T | 1 | a0005c0008t0021g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1189-209T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684714 | |||||||
| chr6:132684721 | T | TA | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-217dupT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684721 | |||||||
| chr6:132684721 | TA | T | 5 | a0001c0001t0001g0194 a0001c0001t0003g0145 a0002c0002t0003g0022 others(2): Show |
7 | HG00639.hp1 HG00738.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189-217delT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684721 | |||||||
| chr6:132684763 | T | A | 1 | a0005c0008t0021g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1189-258A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684763 | |||||||
| chr6:132684822 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1189-317G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684822 | |||||||
| chr6:132684920 | C | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(93): Show |
177 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.1189-415G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684920 | |||||||
| chr6:132684951 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1189-446G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684951 | |||||||
| chr6:132684989 | A | T | 4 | a0008c0007t0008g0118 a0008c0007t0008g0119 a0008c0007t0008g0120 others(1): Show |
4 | HG02723.hp2 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189-484T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132684989 | |||||||
| chr6:132685057 | C | A | 1 | a0004c0004t0017g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1189-552G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685057 | |||||||
| chr6:132685268 | A | G | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-763T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685268 | |||||||
| chr6:132685354 | C | T | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-849G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685354 | |||||||
| chr6:132685487 | C | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(80): Show |
163 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1189-982G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685487 | |||||||
| chr6:132685508 | T | A | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-1003A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685508 | |||||||
| chr6:132685517 | A | C | 1 | a0001c0001t0001g0157 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1189-1012T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685517 | |||||||
| chr6:132685541 | G | C | 1 | a0001c0001t0003g0146 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1189-1036C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685541 | |||||||
| chr6:132685592 | TA | T | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1189-1088delT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685592 | |||||||
| chr6:132685601 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(93): Show |
177 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.1189-1096G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685601 | |||||||
| chr6:132685602 | A | G | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-1097T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685602 | |||||||
| chr6:132685716 | A | G | 1 | a0002c0002t0002g0109 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1189-1211T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685716 | |||||||
| chr6:132685800 | A | G | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-1295T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685800 | |||||||
| chr6:132685819 | T | G | 1 | a0001c0001t0005g0182 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1189-1314A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685819 | |||||||
| chr6:132685951 | C | A | 1 | a0003c0003t0002g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1189-1446G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132685951 | |||||||
| chr6:132686099 | TAGTATA | T | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1189-1600_1189-159 others(10): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686099 | |||||||
| chr6:132686103 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1189-1598T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686103 | |||||||
| chr6:132686113 | C | T | 1 | a0013c0015t0025g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1189-1608G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686113 | |||||||
| chr6:132686140 | A | G | 1 | a0001c0001t0003g0142 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1189-1635T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686140 | |||||||
| chr6:132686147 | A | T | 13 | a0002c0002t0003g0103 a0005c0005t0010g0039 a0005c0005t0010g0123 others(10): Show |
16 | HG02055.hp1 HG02055.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1189-1642T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686147 | |||||||
| chr6:132686257 | G | A | 1 | a0014c0021t0015g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1189-1752C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686257 | |||||||
| chr6:132686290 | T | C | 1 | a0005c0005t0022g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1189-1785A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686290 | |||||||
| chr6:132686340 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1189-1835G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686340 | |||||||
| chr6:132686341 | G | A | 2 | a0002c0002t0003g0009 a0002c0002t0003g0100 |
6 | HG00280.hp1 HG00733.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189-1836C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686341 | |||||||
| chr6:132686395 | C | T | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1189-1890G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686395 | |||||||
| chr6:132686399 | A | G | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-1894T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686399 | |||||||
| chr6:132686445 | C | CA | 14 | a0001c0001t0001g0157 a0005c0005t0010g0039 a0005c0005t0010g0123 others(11): Show |
15 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.1189-1941dupT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686445 | |||||||
| chr6:132686537 | A | G | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1189-2032T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686537 | |||||||
| chr6:132686575 | G | A | 1 | a0001c0001t0001g0045 | 2 | NA18992.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1189-2070C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686575 | |||||||
| chr6:132686602 | C | A | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-2097G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686602 | |||||||
| chr6:132686603 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0167 a0001c0001t0001g0175 others(3): Show |
17 | HG00558.hp1 HG01433.hp2 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1189-2098C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686603 | |||||||
| chr6:132686612 | G | A | 1 | a0003c0003t0002g0060 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1189-2107C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686612 | |||||||
| chr6:132686792 | G | A | 1 | a0002c0002t0002g0110 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1189-2287C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132686792 | |||||||
| chr6:132687048 | T | C | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-2543A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132687048 | |||||||
| chr6:132687051 | T | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(80): Show |
163 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1189-2546A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132687051 | |||||||
| chr6:132687137 | G | C | 1 | a0002c0002t0004g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1189-2632C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132687137 | |||||||
| chr6:132687315 | G | A | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-2810C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132687315 | |||||||
| chr6:132687749 | T | C | 2 | a0002c0002t0003g0095 a0002c0002t0003g0098 |
2 | HG02074.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1189-3244A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132687749 | |||||||
| chr6:132687832 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(80): Show |
163 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1189-3327G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132687832 | |||||||
| chr6:132687868 | G | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(58): Show |
127 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.1189-3363C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132687868 | |||||||
| chr6:132687950 | T | C | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-3445A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132687950 | |||||||
| chr6:132687990 | G | A | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-3485C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132687990 | |||||||
| chr6:132688096 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0169 others(2): Show |
11 | HG01123.hp2 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189-3591A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688096 | |||||||
| chr6:132688107 | A | C | 1 | a0014c0021t0015g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1189-3602T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688107 | |||||||
| chr6:132688144 | C | T | 28 | a0003c0003t0002g0001 a0003c0003t0002g0012 a0003c0003t0002g0019 others(25): Show |
84 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1189-3639G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688144 | |||||||
| chr6:132688145 | A | C | 10 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(7): Show |
11 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189-3640T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688145 | |||||||
| chr6:132688196 | T | C | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-3691A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688196 | |||||||
| chr6:132688416 | G | A | 1 | a0003c0003t0002g0036 | 2 | NA19065.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1188+3807C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688416 | |||||||
| chr6:132688448 | C | T | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+3775G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688448 | |||||||
| chr6:132688525 | A | T | 12 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(9): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1188+3698T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688525 | |||||||
| chr6:132688689 | T | C | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+3534A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688689 | |||||||
| chr6:132688735 | G | A | 1 | a0002c0002t0005g0063 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1188+3488C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688735 | |||||||
| chr6:132688820 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1188+3403C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132688820 | |||||||
| chr6:132689000 | T | C | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1188+3223A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689000 | |||||||
| chr6:132689075 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1188+3148C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689075 | |||||||
| chr6:132689270 | A | AAC | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1188+2951_1188+295 others(6): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689270 | |||||||
| chr6:132689270 | A | AACACACA others(1): Show |
10 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(7): Show |
11 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188+2945_1188+295 others(12): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689270 | |||||||
| chr6:132689270 | A | AACACACA others(3): Show |
3 | a0005c0008t0008g0206 a0005c0008t0010g0207 a0005c0008t0021g0202 |
3 | HG02055.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1188+2943_1188+295 others(14): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689270 | |||||||
| chr6:132689280 | C | G | 17 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0004g0004 others(14): Show |
30 | HG00140.hp2 HG00609.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1188+2943G>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689280 | |||||||
| chr6:132689335 | T | C | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+2888A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689335 | |||||||
| chr6:132689380 | A | G | 1 | a0005c0008t0021g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1188+2843T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689380 | |||||||
| chr6:132689386 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(174): Show |
348 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(345): Show |
intron_variant | MODIFIER | c.1188+2837C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689386 | |||||||
| chr6:132689397 | T | G | 1 | a0003c0003t0002g0087 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1188+2826A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689397 | |||||||
| chr6:132689417 | A | C | 1 | a0002c0002t0004g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1188+2806T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689417 | |||||||
| chr6:132689440 | T | C | 5 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(2): Show |
6 | HG02145.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188+2783A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689440 | |||||||
| chr6:132689538 | G | A | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1188+2685C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689538 | |||||||
| chr6:132689637 | C | T | 1 | a0004c0004t0003g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1188+2586G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689637 | |||||||
| chr6:132689709 | G | A | 17 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0004g0004 others(14): Show |
30 | HG00140.hp2 HG00609.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1188+2514C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689709 | |||||||
| chr6:132689840 | A | G | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1188+2383T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689840 | |||||||
| chr6:132689877 | C | G | 1 | a0002c0002t0003g0104 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1188+2346G>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689877 | |||||||
| chr6:132689974 | T | C | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+2249A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132689974 | |||||||
| chr6:132690090 | G | A | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+2133C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690090 | |||||||
| chr6:132690201 | A | C | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1188+2022T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690201 | |||||||
| chr6:132690302 | C | T | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1188+1921G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690302 | |||||||
| chr6:132690605 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1188+1618G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690605 | |||||||
| chr6:132690613 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1188+1610T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690613 | |||||||
| chr6:132690642 | G | A | 1 | a0002c0002t0004g0071 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1188+1581C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690642 | |||||||
| chr6:132690660 | C | T | 1 | a0005c0008t0008g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1188+1563G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690660 | |||||||
| chr6:132690739 | A | T | 1 | a0001c0001t0005g0052 | 2 | HG02004.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1188+1484T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690739 | |||||||
| chr6:132690756 | CAA | C | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+1465_1188+146 others(6): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690756 | |||||||
| chr6:132690944 | T | C | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+1279A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132690944 | |||||||
| chr6:132691049 | A | G | 1 | a0002c0002t0003g0103 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1188+1174T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691049 | |||||||
| chr6:132691080 | C | T | 17 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0004g0004 others(14): Show |
30 | HG00140.hp2 HG00609.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1188+1143G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691080 | |||||||
| chr6:132691112 | A | G | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+1111T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691112 | |||||||
| chr6:132691183 | A | C | 29 | a0003c0003t0002g0001 a0003c0003t0002g0012 a0003c0003t0002g0019 others(26): Show |
85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1188+1040T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691183 | |||||||
| chr6:132691200 | T | C | 1 | a0002c0002t0003g0114 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1188+1023A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691200 | |||||||
| chr6:132691205 | G | C | 1 | a0002c0002t0004g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1188+1018C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691205 | |||||||
| chr6:132691225 | C | T | 3 | a0004c0004t0017g0150 a0004c0004t0017g0161 a0004c0004t0034g0149 |
3 | HG02559.hp1 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1188+998G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691225 | |||||||
| chr6:132691243 | AAAAC | A | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.1188+976_1188+979d others(6): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691243 | |||||||
| chr6:132691316 | C | G | 1 | a0014c0021t0015g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1188+907G>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691316 | |||||||
| chr6:132691366 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1188+857T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691366 | |||||||
| chr6:132691492 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1188+731C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691492 | |||||||
| chr6:132691534 | A | C | 1 | a0005c0008t0021g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1188+689T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691534 | |||||||
| chr6:132691544 | T | C | 3 | a0004c0004t0003g0126 a0004c0004t0003g0127 a0004c0004t0003g0132 |
3 | HG02486.hp2 HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1188+679A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691544 | |||||||
| chr6:132691642 | A | T | 2 | a0004c0004t0007g0154 a0004c0004t0013g0043 |
3 | HG02280.hp1 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1188+581T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691642 | |||||||
| chr6:132691644 | G | A | 3 | a0002c0013t0003g0061 a0006c0006t0011g0024 a0006c0017t0011g0136 |
5 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1188+579C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691644 | |||||||
| chr6:132691717 | C | T | 1 | a0005c0008t0021g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1188+506G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691717 | |||||||
| chr6:132691787 | G | C | 10 | a0001c0001t0002g0208 a0002c0002t0002g0007 a0002c0002t0002g0013 others(7): Show |
24 | HG00099.hp2 HG00140.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1188+436C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691787 | |||||||
| chr6:132691869 | A | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(177): Show |
353 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.1188+354T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132691869 | |||||||
| chr6:132692003 | C | CA | 24 | a0001c0001t0001g0152 a0001c0001t0001g0183 a0001c0001t0003g0003 others(21): Show |
44 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.1188+219dupT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132692003 | |||||||
| chr6:132692003 | CA | C | 13 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0028g0178 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188+219delT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132692003 | |||||||
| chr6:132692143 | C | A | 9 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(6): Show |
10 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1188+80G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 5/6 | chr6 | 132692143 | |||||||
| chr6:132692587 | G | A | 13 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(10): Show |
14 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.827-3C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 4/6 | chr6 | 132692587 | |||||||
| chr6:132692718 | C | T | 17 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0004g0004 others(14): Show |
30 | HG00140.hp2 HG00609.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.827-134G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 4/6 | chr6 | 132692718 | |||||||
| chr6:132692885 | A | G | 1 | a0002c0013t0003g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.826+139T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 4/6 | chr6 | 132692885 | |||||||
| chr6:132692944 | C | T | 1 | a0003c0003t0002g0083 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.826+80G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 4/6 | chr6 | 132692944 | |||||||
| chr6:132693439 | G | T | 1 | a0005c0008t0021g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.535-124C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693439 | |||||||
| chr6:132693484 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(116): Show |
232 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.535-169G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693484 | |||||||
| chr6:132693622 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.535-307T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693622 | |||||||
| chr6:132693687 | T | G | 1 | a0001c0001t0001g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.534+303A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693687 | |||||||
| chr6:132693717 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.534+273C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693717 | |||||||
| chr6:132693757 | C | T | 1 | a0010c0010t0003g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.534+233G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693757 | |||||||
| chr6:132693772 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.534+218C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693772 | |||||||
| chr6:132693823 | C | T | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.534+167G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693823 | |||||||
| chr6:132693852 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
207 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.534+138C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693852 | |||||||
| chr6:132693879 | C | G | 12 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(9): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.534+111G>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693879 | |||||||
| chr6:132693902 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(80): Show |
163 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.534+88G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 3/6 | chr6 | 132693902 | |||||||
| chr6:132694217 | T | C | 2 | a0002c0002t0001g0030 a0002c0002t0001g0066 |
3 | HG00438.hp2 HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.342-35A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694217 | |||||||
| chr6:132694288 | G | A | 25 | a0002c0013t0003g0061 a0003c0003t0003g0080 a0004c0004t0003g0040 others(22): Show |
29 | HG01070.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.342-106C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694288 | |||||||
| chr6:132694305 | A | G | 3 | a0001c0001t0007g0044 a0001c0001t0007g0148 a0001c0001t0027g0155 |
4 | HG01358.hp2 HG01928.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-123T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694305 | |||||||
| chr6:132694461 | G | A | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.342-279C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694461 | |||||||
| chr6:132694467 | G | A | 49 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0004g0004 others(46): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.342-285C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694467 | |||||||
| chr6:132694523 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-341G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694523 | |||||||
| chr6:132694537 | T | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(177): Show |
353 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.342-355A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694537 | |||||||
| chr6:132694617 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-435C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694617 | |||||||
| chr6:132694619 | C | T | 10 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(7): Show |
11 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.342-437G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694619 | |||||||
| chr6:132694699 | G | GA | 10 | a0001c0001t0001g0173 a0001c0001t0001g0176 a0001c0001t0009g0010 others(7): Show |
14 | HG00609.hp2 HG01255.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.342-518dupT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694699 | |||||||
| chr6:132694699 | G | GAA | 8 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0130 others(5): Show |
9 | HG01070.hp2 HG02602.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.342-519_342-518dup others(2): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694699 | |||||||
| chr6:132694728 | G | A | 1 | a0003c0003t0002g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.342-546C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694728 | |||||||
| chr6:132694812 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-630G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694812 | |||||||
| chr6:132694819 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.342-637A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694819 | |||||||
| chr6:132694861 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-679T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694861 | |||||||
| chr6:132694981 | C | T | 29 | a0003c0003t0002g0001 a0003c0003t0002g0012 a0003c0003t0002g0019 others(26): Show |
85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.342-799G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132694981 | |||||||
| chr6:132695012 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-830G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695012 | |||||||
| chr6:132695020 | C | T | 1 | a0001c0001t0005g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.342-838G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695020 | |||||||
| chr6:132695024 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.342-842G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695024 | |||||||
| chr6:132695087 | G | A | 3 | a0004c0004t0017g0150 a0004c0004t0017g0161 a0004c0004t0034g0149 |
3 | HG02559.hp1 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.342-905C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695087 | |||||||
| chr6:132695161 | A | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-979T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695161 | |||||||
| chr6:132695162 | T | A | 1 | a0001c0001t0004g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.342-980A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695162 | |||||||
| chr6:132695198 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-1016C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695198 | |||||||
| chr6:132695263 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.342-1081C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695263 | |||||||
| chr6:132695336 | C | T | 1 | a0003c0003t0002g0059 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.342-1154G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695336 | |||||||
| chr6:132695546 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-1364A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695546 | |||||||
| chr6:132695558 | C | T | 3 | a0001c0001t0007g0044 a0001c0001t0007g0148 a0001c0001t0027g0155 |
4 | HG01358.hp2 HG01928.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-1376G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695558 | |||||||
| chr6:132695763 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-1581A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695763 | |||||||
| chr6:132695768 | A | G | 3 | a0002c0013t0003g0061 a0006c0006t0011g0024 a0006c0017t0011g0136 |
5 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.342-1586T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695768 | |||||||
| chr6:132695828 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-1646T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695828 | |||||||
| chr6:132695833 | A | C | 1 | a0002c0002t0002g0038 | 2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.342-1651T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695833 | |||||||
| chr6:132695903 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-1721T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132695903 | |||||||
| chr6:132696002 | G | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-1820C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696002 | |||||||
| chr6:132696025 | A | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0050 others(13): Show |
31 | HG00558.hp1 HG00673.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.342-1843T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696025 | |||||||
| chr6:132696074 | G | A | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.342-1892C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696074 | |||||||
| chr6:132696171 | G | GA | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.342-1990dupT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696171 | |||||||
| chr6:132696360 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2178G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696360 | |||||||
| chr6:132696407 | G | C | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.342-2225C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696407 | |||||||
| chr6:132696485 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2303G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696485 | |||||||
| chr6:132696516 | C | A | 10 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(7): Show |
11 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.342-2334G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696516 | |||||||
| chr6:132696520 | T | C | 4 | a0008c0007t0008g0118 a0008c0007t0008g0119 a0008c0007t0008g0120 others(1): Show |
4 | HG02723.hp2 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-2338A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696520 | |||||||
| chr6:132696527 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2345C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696527 | |||||||
| chr6:132696567 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
166 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.342-2385C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696567 | |||||||
| chr6:132696607 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0196 |
3 | HG01081.hp2 HG01255.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.342-2425G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696607 | |||||||
| chr6:132696608 | G | A | 54 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(51): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.342-2426C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696608 | |||||||
| chr6:132696675 | G | GA | 103 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(100): Show |
203 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.342-2494dupT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696675 | |||||||
| chr6:132696675 | GA | G | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.342-2494delT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696675 | |||||||
| chr6:132696685 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.342-2503A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696685 | |||||||
| chr6:132696841 | C | T | 29 | a0003c0003t0002g0001 a0003c0003t0002g0012 a0003c0003t0002g0019 others(26): Show |
85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.342-2659G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696841 | |||||||
| chr6:132696869 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2687A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696869 | |||||||
| chr6:132696921 | C | T | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.342-2739G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696921 | |||||||
| chr6:132696933 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2751C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696933 | |||||||
| chr6:132696937 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.342-2755G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696937 | |||||||
| chr6:132696983 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2801A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696983 | |||||||
| chr6:132696987 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2805A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132696987 | |||||||
| chr6:132697013 | C | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2831G>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697013 | |||||||
| chr6:132697022 | G | A | 2 | a0003c0003t0002g0093 a0009c0009t0003g0210 |
2 | HG02080.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.342-2840C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697022 | |||||||
| chr6:132697061 | C | T | 1 | a0002c0002t0003g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.342-2879G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697061 | |||||||
| chr6:132697062 | G | A | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.342-2880C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697062 | |||||||
| chr6:132697098 | C | T | 1 | a0002c0002t0003g0102 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.342-2916G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697098 | |||||||
| chr6:132697118 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2936C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697118 | |||||||
| chr6:132697126 | AT | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2945delA | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697126 | |||||||
| chr6:132697132 | T | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-2950A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697132 | |||||||
| chr6:132697242 | C | A | 1 | a0002c0002t0015g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.342-3060G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697242 | |||||||
| chr6:132697314 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-3132A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697314 | |||||||
| chr6:132697406 | G | A | 2 | a0003c0003t0006g0037 a0004c0004t0006g0028 |
5 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-3224C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697406 | |||||||
| chr6:132697430 | A | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-3248T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697430 | |||||||
| chr6:132697534 | T | C | 1 | a0005c0008t0008g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.342-3352A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697534 | |||||||
| chr6:132697559 | C | T | 1 | a0003c0003t0002g0012 | 4 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-3377G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697559 | |||||||
| chr6:132697562 | T | C | 10 | a0001c0001t0002g0208 a0002c0002t0002g0007 a0002c0002t0002g0013 others(7): Show |
24 | HG00099.hp2 HG00140.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.342-3380A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697562 | |||||||
| chr6:132697657 | T | C | 1 | a0002c0002t0003g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.342-3475A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697657 | |||||||
| chr6:132697677 | C | A | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.342-3495G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697677 | |||||||
| chr6:132697743 | T | C | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.342-3561A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697743 | |||||||
| chr6:132697805 | C | A | 1 | a0002c0002t0003g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.342-3623G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697805 | |||||||
| chr6:132697808 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0209 |
3 | HG02451.hp1 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.342-3626G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697808 | |||||||
| chr6:132697810 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(103): Show |
206 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.342-3628C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697810 | |||||||
| chr6:132697894 | T | C | 1 | a0003c0003t0003g0080 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.342-3712A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132697894 | |||||||
| chr6:132698060 | C | T | 20 | a0001c0001t0001g0190 a0001c0001t0003g0003 a0001c0001t0003g0015 others(17): Show |
40 | HG00558.hp1 HG00621.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.342-3878G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698060 | |||||||
| chr6:132698064 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-3882A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698064 | |||||||
| chr6:132698342 | T | C | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.342-4160A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698342 | |||||||
| chr6:132698388 | A | G | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.342-4206T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698388 | |||||||
| chr6:132698448 | G | T | 1 | a0002c0002t0004g0032 | 2 | NA19007.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.342-4266C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698448 | |||||||
| chr6:132698543 | A | G | 32 | a0003c0003t0002g0001 a0003c0003t0002g0012 a0003c0003t0002g0019 others(29): Show |
88 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.342-4361T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698543 | |||||||
| chr6:132698598 | A | C | 2 | a0001c0001t0002g0208 a0002c0002t0002g0101 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.342-4416T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698598 | |||||||
| chr6:132698613 | A | G | 10 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(7): Show |
11 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.342-4431T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698613 | |||||||
| chr6:132698615 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-4433T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698615 | |||||||
| chr6:132698618 | A | G | 10 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(7): Show |
11 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.342-4436T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698618 | |||||||
| chr6:132698713 | G | A | 10 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(7): Show |
11 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.342-4531C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698713 | |||||||
| chr6:132698719 | C | T | 54 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(51): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.342-4537G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698719 | |||||||
| chr6:132698801 | C | T | 1 | a0002c0002t0003g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.342-4619G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132698801 | |||||||
| chr6:132699193 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.342-5011C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699193 | |||||||
| chr6:132699276 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-5094C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699276 | |||||||
| chr6:132699359 | C | T | 2 | a0001c0001t0003g0015 a0018c0024t0003g0211 |
5 | HG00735.hp1 HG01934.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.342-5177G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699359 | |||||||
| chr6:132699416 | T | A | 4 | a0008c0007t0008g0118 a0008c0007t0008g0119 a0008c0007t0008g0120 others(1): Show |
4 | HG02723.hp2 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-5234A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699416 | |||||||
| chr6:132699645 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.342-5463T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699645 | |||||||
| chr6:132699701 | A | G | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.342-5519T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699701 | |||||||
| chr6:132699788 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
205 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.342-5606C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699788 | |||||||
| chr6:132699932 | G | A | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.342-5750C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699932 | |||||||
| chr6:132699945 | T | C | 54 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(51): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.342-5763A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699945 | |||||||
| chr6:132699963 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0157 a0001c0001t0001g0159 |
4 | NA18964.hp1 NA18975.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-5781A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132699963 | |||||||
| chr6:132700037 | A | C | 1 | a0004c0004t0001g0137 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.342-5855T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700037 | |||||||
| chr6:132700122 | G | T | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.342-5940C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700122 | |||||||
| chr6:132700137 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.342-5955T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700137 | |||||||
| chr6:132700169 | C | T | 1 | a0002c0002t0003g0100 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.342-5987G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700169 | |||||||
| chr6:132700243 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(103): Show |
206 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.342-6061A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700243 | |||||||
| chr6:132700294 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(78): Show |
160 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.342-6112A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700294 | |||||||
| chr6:132700310 | TA | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(103): Show |
206 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.342-6129delT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700310 | |||||||
| chr6:132700325 | A | G | 1 | a0002c0002t0002g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.342-6143T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700325 | |||||||
| chr6:132700346 | C | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(103): Show |
206 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.342-6164G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700346 | |||||||
| chr6:132700349 | C | T | 19 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0025 others(16): Show |
39 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.342-6167G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700349 | |||||||
| chr6:132700376 | A | T | 1 | a0001c0001t0001g0048 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.342-6194T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700376 | |||||||
| chr6:132700515 | C | G | 1 | a0004c0004t0003g0131 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.342-6333G>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700515 | |||||||
| chr6:132700598 | A | G | 2 | a0004c0004t0007g0154 a0004c0004t0013g0043 |
3 | HG02280.hp1 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.342-6416T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700598 | |||||||
| chr6:132700618 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.342-6436G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700618 | |||||||
| chr6:132700772 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(88): Show |
173 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.342-6590A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700772 | |||||||
| chr6:132700824 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.342-6642C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700824 | |||||||
| chr6:132700848 | C | T | 1 | a0002c0002t0004g0072 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.342-6666G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700848 | |||||||
| chr6:132700901 | G | A | 6 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(3): Show |
7 | HG02145.hp1 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.342-6719C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132700901 | |||||||
| chr6:132701016 | A | G | 8 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(5): Show |
9 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.342-6834T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701016 | |||||||
| chr6:132701058 | A | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(118): Show |
224 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.342-6876T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701058 | |||||||
| chr6:132701100 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
260 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(257): Show |
intron_variant | MODIFIER | c.342-6918G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701100 | |||||||
| chr6:132701329 | T | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(118): Show |
224 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.342-7147A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701329 | |||||||
| chr6:132701439 | A | T | 2 | a0004c0004t0017g0150 a0004c0004t0034g0149 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.342-7257T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701439 | |||||||
| chr6:132701519 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.342-7337T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701519 | |||||||
| chr6:132701622 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(115): Show |
221 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.342-7440T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701622 | |||||||
| chr6:132701714 | A | G | 21 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(18): Show |
35 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.342-7532T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701714 | |||||||
| chr6:132701753 | G | A | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.342-7571C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701753 | |||||||
| chr6:132701780 | C | T | 8 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(5): Show |
9 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.342-7598G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701780 | |||||||
| chr6:132701897 | A | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(115): Show |
221 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.342-7715T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701897 | |||||||
| chr6:132701961 | C | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0153 a0001c0001t0001g0158 |
4 | NA18950.hp2 NA18988.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-7779G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132701961 | |||||||
| chr6:132702119 | T | C | 1 | a0002c0002t0001g0031 | 2 | HG00408.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.342-7937A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702119 | |||||||
| chr6:132702242 | T | A | 1 | a0003c0003t0002g0090 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.342-8060A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702242 | |||||||
| chr6:132702256 | G | A | 2 | a0002c0002t0004g0076 a0002c0002t0004g0077 |
2 | NA19002.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.342-8074C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702256 | |||||||
| chr6:132702392 | C | T | 8 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(5): Show |
9 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.342-8210G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702392 | |||||||
| chr6:132702420 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.342-8238C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702420 | |||||||
| chr6:132702447 | G | A | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.342-8265C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702447 | |||||||
| chr6:132702509 | G | A | 18 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(15): Show |
32 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.342-8327C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702509 | |||||||
| chr6:132702589 | C | G | 22 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(19): Show |
36 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.342-8407G>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702589 | |||||||
| chr6:132702648 | G | A | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.342-8466C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702648 | |||||||
| chr6:132702651 | C | T | 1 | a0005c0008t0021g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.342-8469G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702651 | |||||||
| chr6:132702889 | G | C | 19 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(16): Show |
33 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.342-8707C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132702889 | |||||||
| chr6:132703030 | A | C | 1 | a0001c0001t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.341+8679T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132703030 | |||||||
| chr6:132703044 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(115): Show |
221 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.341+8665C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132703044 | |||||||
| chr6:132703247 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+8462T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132703247 | |||||||
| chr6:132703318 | A | G | 3 | a0002c0013t0003g0061 a0006c0006t0011g0024 a0006c0017t0011g0136 |
5 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+8391T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132703318 | |||||||
| chr6:132703365 | C | CATAGACA others(1): Show |
29 | a0003c0003t0002g0001 a0003c0003t0002g0012 a0003c0003t0002g0019 others(26): Show |
85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.341+8343_341+8344i others(10): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132703365 | |||||||
| chr6:132703453 | T | C | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.341+8256A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132703453 | |||||||
| chr6:132703841 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(109): Show |
211 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(208): Show |
intron_variant | MODIFIER | c.341+7868G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132703841 | |||||||
| chr6:132703856 | G | A | 1 | a0004c0004t0001g0137 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.341+7853C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132703856 | |||||||
| chr6:132703863 | C | T | 3 | a0004c0004t0017g0150 a0004c0004t0017g0161 a0004c0004t0034g0149 |
3 | HG02559.hp1 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.341+7846G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132703863 | |||||||
| chr6:132704055 | T | G | 1 | a0008c0007t0008g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.341+7654A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704055 | |||||||
| chr6:132704164 | A | C | 3 | a0003c0003t0002g0012 a0003c0003t0002g0058 a0003c0003t0002g0082 |
6 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+7545T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704164 | |||||||
| chr6:132704164 | A | T | 1 | a0002c0002t0003g0023 | 3 | HG03688.hp2 HG03704.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.341+7545T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704164 | |||||||
| chr6:132704224 | T | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
168 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.341+7485A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704224 | |||||||
| chr6:132704281 | T | A | 1 | a0015c0018t0008g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.341+7428A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704281 | |||||||
| chr6:132704420 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0169 a0005c0005t0023g0168 |
5 | HG01123.hp2 HG02615.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+7289T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704420 | |||||||
| chr6:132704498 | T | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(115): Show |
221 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.341+7211A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704498 | |||||||
| chr6:132704545 | T | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(115): Show |
221 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.341+7164A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704545 | |||||||
| chr6:132704563 | T | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(178): Show |
355 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.341+7146A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704563 | |||||||
| chr6:132704576 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.341+7133C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704576 | |||||||
| chr6:132704637 | A | G | 1 | a0013c0015t0025g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.341+7072T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704637 | |||||||
| chr6:132704676 | C | A | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+7033G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704676 | |||||||
| chr6:132704744 | C | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(149): Show |
270 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.341+6965G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704744 | |||||||
| chr6:132704745 | CA | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+6963delT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704745 | |||||||
| chr6:132704770 | T | G | 8 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(5): Show |
9 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.341+6939A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704770 | |||||||
| chr6:132704801 | A | T | 8 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(5): Show |
9 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.341+6908T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704801 | |||||||
| chr6:132704803 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(97): Show |
185 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.341+6906C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132704803 | |||||||
| chr6:132705007 | G | A | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(178): Show |
355 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.341+6702C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705007 | |||||||
| chr6:132705051 | C | CA | 15 | a0001c0001t0001g0189 a0001c0001t0004g0203 a0001c0001t0004g0204 others(12): Show |
28 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.341+6657dupT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705051 | |||||||
| chr6:132705190 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.341+6519T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705190 | |||||||
| chr6:132705193 | AT | A | 29 | a0003c0003t0002g0001 a0003c0003t0002g0012 a0003c0003t0002g0019 others(26): Show |
85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.341+6515delA | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705193 | |||||||
| chr6:132705218 | A | T | 1 | a0002c0002t0003g0098 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.341+6491T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705218 | |||||||
| chr6:132705300 | C | T | 19 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(16): Show |
33 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.341+6409G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705300 | |||||||
| chr6:132705322 | T | C | 1 | a0001c0001t0003g0143 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.341+6387A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705322 | |||||||
| chr6:132705396 | A | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+6313T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705396 | |||||||
| chr6:132705480 | T | C | 1 | a0003c0003t0002g0091 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.341+6229A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705480 | |||||||
| chr6:132705550 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
168 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.341+6159G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705550 | |||||||
| chr6:132705761 | A | G | 1 | a0002c0002t0004g0032 | 2 | NA19007.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.341+5948T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132705761 | |||||||
| chr6:132706017 | C | T | 1 | a0002c0013t0003g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.341+5692G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706017 | |||||||
| chr6:132706038 | C | T | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.341+5671G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706038 | |||||||
| chr6:132706067 | T | G | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+5642A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706067 | |||||||
| chr6:132706148 | C | T | 2 | a0001c0001t0003g0042 a0001c0001t0003g0205 |
3 | HG01361.hp1 HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.341+5561G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706148 | |||||||
| chr6:132706268 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.341+5441G>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706268 | |||||||
| chr6:132706559 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341+5150C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706559 | |||||||
| chr6:132706587 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.341+5122A>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706587 | |||||||
| chr6:132706729 | T | C | 6 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(3): Show |
7 | HG02145.hp1 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+4980A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706729 | |||||||
| chr6:132706743 | G | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
260 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(257): Show |
intron_variant | MODIFIER | c.341+4966C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706743 | |||||||
| chr6:132706835 | A | G | 1 | a0002c0002t0002g0013 | 4 | NA18939.hp1 NA18940.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.341+4874T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706835 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2118): Show |
1 | a0004c0004t0017g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2127): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2117): Show |
1 | a0004c0004t0034g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2126): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2118): Show |
1 | a0004c0004t0017g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2127): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2045): Show |
1 | a0009c0009t0003g0210 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2054): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2044): Show |
1 | a0009c0009t0003g0053 | 2 | NA19011.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.341+4840_341+4841i others(2053): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2027): Show |
1 | a0001c0001t0003g0041 | 2 | HG01978.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.341+4840_341+4841i others(2036): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2027): Show |
1 | a0017c0023t0003g0147 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2036): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2025): Show |
1 | a0010c0010t0003g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2034): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2026): Show |
12 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0042 others(9): Show |
28 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.341+4840_341+4841i others(2035): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2217): Show |
1 | a0004c0004t0003g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2226): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2212): Show |
1 | a0004c0004t0003g0135 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2221): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2211): Show |
1 | a0004c0004t0003g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2220): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2212): Show |
1 | a0004c0004t0003g0131 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2221): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2209): Show |
1 | a0004c0004t0003g0127 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2218): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2209): Show |
4 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0129 others(1): Show |
5 | HG01070.hp2 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+4840_341+4841i others(2218): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2208): Show |
2 | a0004c0004t0003g0126 a0004c0004t0003g0132 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.341+4840_341+4841i others(2217): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2209): Show |
1 | a0004c0004t0014g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2218): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2131): Show |
1 | a0005c0005t0010g0123 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2140): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2129): Show |
3 | a0005c0005t0010g0039 a0005c0005t0014g0121 a0005c0005t0020g0122 |
4 | HG02818.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.341+4840_341+4841i others(2138): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2130): Show |
1 | a0005c0005t0022g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2139): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2124): Show |
1 | a0015c0018t0008g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2133): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2128): Show |
1 | a0005c0008t0010g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2137): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2020): Show |
1 | a0001c0001t0003g0144 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2029): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706868 | C | CAAAAGAA others(2123): Show |
1 | a0005c0008t0008g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.341+4840_341+4841i others(2132): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706868 | |||||||
| chr6:132706873 | G | GAAGTTAT others(2128): Show |
1 | a0005c0008t0021g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.341+4835_341+4836i others(2137): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706873 | |||||||
| chr6:132706873 | G | GAAGTTAT others(2124): Show |
1 | a0002c0013t0003g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.341+4835_341+4836i others(2133): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706873 | |||||||
| chr6:132706873 | G | GAAGTTAT others(2122): Show |
1 | a0006c0017t0011g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.341+4835_341+4836i others(2131): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706873 | |||||||
| chr6:132706873 | G | GAAGTTAT others(2123): Show |
1 | a0006c0006t0011g0024 | 3 | HG02055.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.341+4835_341+4836i others(2132): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706873 | |||||||
| chr6:132706954 | T | C | 48 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(45): Show |
70 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.341+4755A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706954 | |||||||
| chr6:132706981 | T | C | 33 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(30): Show |
54 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(51): Show |
intron_variant | MODIFIER | c.341+4728A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132706981 | |||||||
| chr6:132707015 | T | C | 1 | a0004c0004t0003g0135 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.341+4694A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707015 | |||||||
| chr6:132707055 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.341+4654G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707055 | |||||||
| chr6:132707056 | G | A | 29 | a0003c0003t0002g0001 a0003c0003t0002g0012 a0003c0003t0002g0019 others(26): Show |
85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.341+4653C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707056 | |||||||
| chr6:132707155 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.341+4554C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707155 | |||||||
| chr6:132707174 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.341+4535G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707174 | |||||||
| chr6:132707226 | C | CA | 31 | a0001c0001t0001g0117 a0001c0001t0001g0165 a0001c0001t0001g0166 others(28): Show |
91 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.341+4482dupT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707226 | |||||||
| chr6:132707226 | C | CAA | 109 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(106): Show |
204 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.341+4481_341+4482d others(4): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707226 | |||||||
| chr6:132707226 | C | CAAA | 15 | a0001c0001t0001g0160 a0001c0001t0001g0190 a0001c0001t0001g0191 others(12): Show |
16 | HG00558.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.341+4480_341+4482d others(5): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707226 | |||||||
| chr6:132707226 | C | CAAAA | 23 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(20): Show |
41 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.341+4479_341+4482d others(6): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707226 | |||||||
| chr6:132707249 | A | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+4460T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707249 | |||||||
| chr6:132707269 | C | T | 1 | a0002c0002t0004g0069 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.341+4440G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707269 | |||||||
| chr6:132707309 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.341+4400A>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707309 | |||||||
| chr6:132707385 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.341+4324C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707385 | |||||||
| chr6:132707414 | C | A | 27 | a0002c0013t0003g0061 a0003c0003t0003g0080 a0004c0004t0003g0040 others(24): Show |
31 | HG01070.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.341+4295G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707414 | |||||||
| chr6:132707681 | A | G | 6 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(3): Show |
7 | HG02145.hp1 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+4028T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707681 | |||||||
| chr6:132707731 | G | T | 2 | a0002c0002t0003g0022 a0002c0002t0003g0097 |
4 | HG00639.hp1 HG00738.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.341+3978C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707731 | |||||||
| chr6:132707747 | A | G | 16 | a0002c0013t0003g0061 a0004c0004t0001g0137 a0004c0004t0017g0150 others(13): Show |
19 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.341+3962T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707747 | |||||||
| chr6:132707900 | A | G | 8 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(5): Show |
9 | HG02055.hp2 HG02145.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.341+3809T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132707900 | |||||||
| chr6:132708010 | T | C | 2 | a0001c0001t0003g0145 a0017c0023t0003g0147 |
2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.341+3699A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708010 | |||||||
| chr6:132708104 | C | T | 1 | a0001c0001t0030g0163 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.341+3605G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708104 | |||||||
| chr6:132708110 | C | A | 45 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(42): Show |
67 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.341+3599G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708110 | |||||||
| chr6:132708137 | G | C | 1 | a0013c0015t0025g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.341+3572C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708137 | |||||||
| chr6:132708190 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0197 a0001c0001t0007g0199 others(1): Show |
7 | HG00673.hp2 HG02040.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+3519A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708190 | |||||||
| chr6:132708278 | G | T | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.341+3431C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708278 | |||||||
| chr6:132708279 | C | T | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.341+3430G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708279 | |||||||
| chr6:132708303 | A | G | 45 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(42): Show |
67 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.341+3406T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708303 | |||||||
| chr6:132708474 | A | T | 7 | a0002c0013t0003g0061 a0004c0004t0017g0150 a0004c0004t0017g0161 others(4): Show |
9 | HG02055.hp1 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.341+3235T>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708474 | |||||||
| chr6:132708590 | A | C | 1 | a0002c0002t0001g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.341+3119T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708590 | |||||||
| chr6:132708683 | G | A | 3 | a0004c0004t0017g0150 a0004c0004t0017g0161 a0004c0004t0034g0149 |
3 | HG02559.hp1 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.341+3026C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708683 | |||||||
| chr6:132708824 | A | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0162 |
5 | HG02572.hp1 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+2885T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708824 | |||||||
| chr6:132708828 | C | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+2881G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708828 | |||||||
| chr6:132708829 | G | A | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.341+2880C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708829 | |||||||
| chr6:132708909 | G | C | 21 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(18): Show |
35 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.341+2800C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132708909 | |||||||
| chr6:132709076 | C | T | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.341+2633G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709076 | |||||||
| chr6:132709094 | A | G | 1 | a0002c0002t0004g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.341+2615T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709094 | |||||||
| chr6:132709152 | A | C | 1 | a0005c0008t0021g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.341+2557T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709152 | |||||||
| chr6:132709218 | TGATA | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
261 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(258): Show |
intron_variant | MODIFIER | c.341+2487_341+2490d others(6): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709218 | |||||||
| chr6:132709250 | C | A | 45 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(42): Show |
67 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.341+2459G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709250 | |||||||
| chr6:132709260 | CT | C | 45 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(42): Show |
67 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.341+2448delA | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709260 | |||||||
| chr6:132709353 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(122): Show |
225 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(222): Show |
intron_variant | MODIFIER | c.341+2356A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709353 | |||||||
| chr6:132709397 | C | T | 1 | a0002c0013t0003g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.341+2312G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709397 | |||||||
| chr6:132709398 | G | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(55): Show |
120 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(117): Show |
intron_variant | MODIFIER | c.341+2311C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709398 | |||||||
| chr6:132709571 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(122): Show |
225 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(222): Show |
intron_variant | MODIFIER | c.341+2138G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709571 | |||||||
| chr6:132709572 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(122): Show |
225 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(222): Show |
intron_variant | MODIFIER | c.341+2137T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709572 | |||||||
| chr6:132709620 | C | T | 3 | a0002c0013t0003g0061 a0006c0006t0011g0024 a0006c0017t0011g0136 |
5 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+2089G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709620 | |||||||
| chr6:132709661 | CA | C | 22 | a0001c0001t0004g0203 a0001c0001t0004g0204 a0002c0002t0003g0034 others(19): Show |
36 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+2047delT | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709661 | |||||||
| chr6:132709661 | CAA | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(120): Show |
223 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(220): Show |
intron_variant | MODIFIER | c.341+2046_341+2047d others(4): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709661 | |||||||
| chr6:132709676 | G | A | 1 | a0003c0003t0002g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.341+2033C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709676 | |||||||
| chr6:132709686 | G | A | 3 | a0008c0007t0008g0118 a0008c0007t0008g0119 a0008c0007t0008g0120 |
3 | HG02723.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.341+2023C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709686 | |||||||
| chr6:132709968 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.341+1741T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709968 | |||||||
| chr6:132709972 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
226 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(223): Show |
intron_variant | MODIFIER | c.341+1737A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132709972 | |||||||
| chr6:132710068 | A | G | 1 | a0001c0001t0007g0148 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.341+1641T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132710068 | |||||||
| chr6:132710073 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.341+1636C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132710073 | |||||||
| chr6:132710113 | C | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(124): Show |
227 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(224): Show |
intron_variant | MODIFIER | c.341+1596G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132710113 | |||||||
| chr6:132710241 | G | A | 1 | a0003c0003t0002g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.341+1468C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132710241 | |||||||
| chr6:132710302 | G | A | 1 | a0002c0002t0016g0079 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.341+1407C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132710302 | |||||||
| chr6:132710375 | G | A | 12 | a0003c0003t0003g0080 a0004c0004t0003g0040 a0004c0004t0003g0126 others(9): Show |
13 | HG01070.hp2 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.341+1334C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132710375 | |||||||
| chr6:132710448 | G | A | 3 | a0002c0013t0003g0061 a0006c0006t0011g0024 a0006c0017t0011g0136 |
5 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+1261C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132710448 | |||||||
| chr6:132710529 | G | C | 1 | a0002c0002t0003g0114 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.341+1180C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132710529 | |||||||
| chr6:132710832 | T | C | 3 | a0002c0013t0003g0061 a0006c0006t0011g0024 a0006c0017t0011g0136 |
5 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+877A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132710832 | |||||||
| chr6:132711116 | A | G | 2 | a0004c0004t0017g0150 a0004c0004t0034g0149 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.341+593T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711116 | |||||||
| chr6:132711133 | T | C | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+576A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711133 | |||||||
| chr6:132711318 | C | CT | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
166 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(163): Show |
intron_variant | MODIFIER | c.341+390dupA | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711318 | |||||||
| chr6:132711393 | C | T | 1 | a0002c0002t0003g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.341+316G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711393 | |||||||
| chr6:132711413 | A | G | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.341+296T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711413 | |||||||
| chr6:132711423 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.341+286A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711423 | |||||||
| chr6:132711472 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(82): Show |
165 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.341+237C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711472 | |||||||
| chr6:132711529 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
261 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(258): Show |
intron_variant | MODIFIER | c.341+180G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711529 | |||||||
| chr6:132711575 | C | T | 17 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(14): Show |
35 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.341+134G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711575 | |||||||
| chr6:132711582 | G | C | 12 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(9): Show |
13 | HG02055.hp2 HG02145.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.341+127C>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711582 | |||||||
| chr6:132711620 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
233 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.341+89T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711620 | |||||||
| chr6:132711658 | G | A | 18 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(15): Show |
36 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+51C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 2/6 | chr6 | 132711658 | |||||||
| chr6:132711866 | GGGGGGCC others(36): Show |
G | 1 | a0001c0001t0007g0148 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.211-70_211-28delGT others(41): Show |
VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132711866 | |||||||
| chr6:132712139 | A | AT | 17 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0041 others(14): Show |
35 | HG00621.hp2 HG00735.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.211-301dupA | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712139 | |||||||
| chr6:132712219 | G | A | 6 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(3): Show |
7 | HG02145.hp1 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-380C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712219 | |||||||
| chr6:132712230 | A | G | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211-391T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712230 | |||||||
| chr6:132712261 | C | T | 1 | a0004c0004t0001g0137 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.211-422G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712261 | |||||||
| chr6:132712262 | G | A | 1 | a0013c0015t0025g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.211-423C>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712262 | |||||||
| chr6:132712392 | C | T | 2 | a0006c0006t0011g0024 a0006c0017t0011g0136 |
4 | HG02055.hp1 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-553G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712392 | |||||||
| chr6:132712482 | T | C | 2 | a0005c0008t0008g0206 a0005c0008t0010g0207 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211-643A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712482 | |||||||
| chr6:132712553 | C | T | 11 | a0004c0004t0003g0040 a0004c0004t0003g0126 a0004c0004t0003g0127 others(8): Show |
12 | HG02486.hp2 HG02602.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.211-714G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712553 | |||||||
| chr6:132712712 | C | T | 9 | a0005c0005t0010g0039 a0005c0005t0010g0123 a0005c0005t0014g0121 others(6): Show |
10 | HG02145.hp1 HG02723.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-873G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712712 | |||||||
| chr6:132712726 | G | T | 4 | a0003c0003t0002g0019 a0003c0003t0002g0059 a0003c0003t0002g0060 others(1): Show |
7 | HG02273.hp1 HG02293.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-887C>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712726 | |||||||
| chr6:132712737 | A | G | 1 | a0008c0007t0008g0118 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.211-898T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712737 | |||||||
| chr6:132712937 | A | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(177): Show |
351 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.210+889T>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132712937 | |||||||
| chr6:132713319 | C | T | 1 | a0003c0003t0002g0058 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.210+507G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132713319 | |||||||
| chr6:132713427 | T | C | 1 | a0013c0015t0025g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.210+399A>G | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132713427 | |||||||
| chr6:132713446 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.210+380T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132713446 | |||||||
| chr6:132713498 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.210+328G>T | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132713498 | |||||||
| chr6:132713635 | C | T | 1 | a0003c0003t0002g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.210+191G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132713635 | |||||||
| chr6:132713742 | C | T | 1 | a0010c0010t0001g0116 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.210+84G>A | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132713742 | |||||||
| chr6:132713815 | A | G | 1 | a0002c0002t0003g0056 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.210+11T>C | VNN1 | ENSG00000112299.8 | transcript | ENST00000367928.5 | protein_coding | 1/6 | chr6 | 132713815 |