Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57176 |
| ensemblid | ENSG00000137411.19 |
| hgncid | 21642 |
| symbol | VARS2 |
| name | valyl-tRNA synthetase 2, mitochondrial |
| refseq_nuc | NM_020442.6 |
| refseq_prot | NP_065175.4 |
| ensembl_nuc | ENST00000676266.1 |
| ensembl_prot | ENSP00000502585.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 30914238 |
| end | 30926459 |
| strand | + |
| ver | v1.2 |
| region | chr6:30914238-30926459 |
| region5000 | chr6:30909238-30931459 |
| regionname0 | VARS2_chr6_30914238_30926459 |
| regionname5000 | VARS2_chr6_30909238_30931459 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1063 | 166 | 22 | 26 | 93 | 7 | 17 | 69 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0002 | 0/0 | 1063 | 89 | 10 | 22 | 38 | 5 | 14 | 31 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0003 | 0/0 | 1063 | 81 | 27 | 18 | 30 | 2 | 4 | 27 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0004 | 0/0 | 1063 | 29 | 8 | 6 | 2 | 4 | 9 | 2 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0005 | 0/0 | 1063 | 27 | 13 | 4 | 9 | 0 | 1 | 5 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0006 | 0/0 | 1063 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0007 | 0/0 | 1063 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0008 | 0/0 | 1063 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0009 | 0/0 | 1063 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0010 | 0/0 | 1063 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0011 | 0/0 | 1063 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0012 | 0/0 | 1063 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0013 | 0/0 | 1063 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0014 | 0/0 | 1063 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0015 | 0/0 | 1063 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0016 | 0/0 | 1063 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0017 | 0/0 | 1063 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0018 | 0/0 | 1063 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| a0019 | 0/0 | 1063 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | MPHLP others(1058): Show |
chr6 | 30909238 | 30931459 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3189 | 141 | 7 | 23 | 89 | 7 | 14 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0001c0006 | 0/0 | 3189 | 21 | 13 | 2 | 3 | 0 | 3 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0001c0012 | 0/0 | 3189 | 3 | 2 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0001c0024 | 0/0 | 3189 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0002c0002 | 0/0 | 3189 | 83 | 10 | 21 | 38 | 5 | 9 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0002c0008 | 0/0 | 3189 | 5 | 0 | 0 | 0 | 0 | 5 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0002c0028 | 0/0 | 3189 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0003c0003 | 0/0 | 3189 | 78 | 24 | 18 | 30 | 2 | 4 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0003c0013 | 0/0 | 3189 | 2 | 2 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0003c0015 | 0/0 | 3189 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0004c0005 | 0/0 | 3189 | 25 | 8 | 6 | 2 | 4 | 5 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0004c0009 | 0/0 | 3189 | 4 | 0 | 0 | 0 | 0 | 4 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0005c0004 | 0/0 | 3189 | 27 | 13 | 4 | 9 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0006c0007 | 0/0 | 3189 | 6 | 6 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0007c0010 | 0/0 | 3189 | 4 | 0 | 0 | 4 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0007c0021 | 0/0 | 3189 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0008c0011 | 0/0 | 3189 | 3 | 3 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0009c0017 | 0/0 | 3189 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0010c0019 | 0/0 | 3189 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0011c0027 | 0/0 | 3189 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0012c0014 | 0/0 | 3189 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0013c0018 | 0/0 | 3189 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0014c0026 | 0/0 | 3189 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0015c0020 | 0/0 | 3189 | 1 | 0 | 0 | 0 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0016c0016 | 0/0 | 3189 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0017c0023 | 0/0 | 3189 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0018c0022 | 0/0 | 3189 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 | ||
| a0019c0025 | 0/0 | 3189 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | ATGCC others(3184): Show |
chr6 | 30909238 | 30931459 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3575 | 140 | 7 | 22 | 89 | 7 | 14 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0001c0001t0002 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0001c0006t0001 | 0/0 | 3575 | 21 | 13 | 2 | 3 | 0 | 3 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0001c0012t0001 | 0/0 | 3575 | 3 | 2 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0001c0024t0001 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0002c0002t0001 | 0/0 | 3575 | 83 | 10 | 21 | 38 | 5 | 9 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0002c0008t0001 | 0/0 | 3575 | 5 | 0 | 0 | 0 | 0 | 5 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0002c0028t0001 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0003c0003t0001 | 0/0 | 3575 | 78 | 24 | 18 | 30 | 2 | 4 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0003c0013t0001 | 0/0 | 3575 | 2 | 2 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0003c0015t0001 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0004c0005t0001 | 0/0 | 3575 | 25 | 8 | 6 | 2 | 4 | 5 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0004c0009t0001 | 0/0 | 3575 | 4 | 0 | 0 | 0 | 0 | 4 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0005c0004t0001 | 0/0 | 3575 | 27 | 13 | 4 | 9 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0006c0007t0001 | 0/0 | 3575 | 6 | 6 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0007c0010t0001 | 0/0 | 3575 | 4 | 0 | 0 | 4 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0007c0021t0001 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0008c0011t0001 | 0/0 | 3575 | 3 | 3 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0009c0017t0001 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0010c0019t0001 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0011c0027t0001 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0012c0014t0001 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0013c0018t0001 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0014c0026t0001 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0015c0020t0001 | 0/0 | 3575 | 1 | 0 | 0 | 0 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0016c0016t0001 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0017c0023t0001 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0018c0022t0001 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| a0019c0025t0001 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | GCCCC others(3570): Show |
chr6 | 30909238 | 30931459 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 60 | 4 | 5 | 39 | 5 | 7 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0006 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0007 | 0/0 | 14 | 1 | 7 | 5 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0009 | 0/0 | 13 | 0 | 7 | 6 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0012 | 0/0 | 10 | 0 | 0 | 4 | 1 | 5 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0019 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0001g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0006t0001g0014 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0006t0001g0017 | 0/0 | 6 | 3 | 0 | 3 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0006t0001g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0006t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0006t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0012t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0012t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0001c0024t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0002 | 0/0 | 49 | 1 | 15 | 26 | 2 | 5 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0004 | 0/0 | 20 | 8 | 3 | 5 | 1 | 3 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0020 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0008t0001g0002 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0008t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0002c0028t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0003 | 0/0 | 26 | 5 | 2 | 18 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0005 | 0/0 | 20 | 9 | 7 | 0 | 2 | 2 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0008 | 0/0 | 15 | 0 | 4 | 10 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0016 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0013t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0003c0015t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0004c0005t0001g0011 | 0/0 | 7 | 2 | 4 | 0 | 1 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0004c0005t0001g0015 | 0/0 | 8 | 3 | 1 | 1 | 1 | 2 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0004c0005t0001g0021 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0004c0005t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0004c0005t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0004c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0004c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0004c0009t0001g0011 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0005c0004t0001g0010 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0005c0004t0001g0013 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0005c0004t0001g0022 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0005c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0005c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0006c0007t0001g0018 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0007c0010t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0007c0021t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0008c0011t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0009c0017t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0010c0019t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0011c0027t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0012c0014t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0013c0018t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0014c0026t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0015c0020t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0016c0016t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0017c0023t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0018c0022t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| a0019c0025t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00099 | hp2 | a0004 | c0005 | t0001 | g0011 | EUR | GBR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0058 | EUR | FIN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00323 | hp1 | a0004 | c0005 | t0001 | g0015 | EUR | FIN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00323 | hp2 | a0004 | c0005 | t0001 | g0065 | EUR | FIN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00609 | hp2 | a0005 | c0004 | t0001 | g0010 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00621 | hp2 | a0009 | c0017 | t0001 | g0071 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00639 | hp1 | a0002 | c0028 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0032 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00673 | hp2 | a0005 | c0004 | t0001 | g0010 | EAS | CHS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00735 | hp1 | a0005 | c0004 | t0001 | g0022 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00738 | hp1 | a0004 | c0005 | t0001 | g0011 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG00741 | hp2 | a0010 | c0019 | t0001 | g0067 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01069 | hp2 | a0004 | c0005 | t0001 | g0011 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01070 | hp1 | a0004 | c0005 | t0001 | g0011 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0032 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01106 | hp2 | a0005 | c0004 | t0001 | g0022 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01243 | hp2 | a0001 | c0006 | t0001 | g0014 | AMR | PUR | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0033 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0008 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0033 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01258 | hp2 | a0003 | c0003 | t0001 | g0008 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01261 | hp2 | a0004 | c0005 | t0001 | g0035 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01361 | hp2 | a0001 | c0006 | t0001 | g0038 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01433 | hp1 | a0004 | c0005 | t0001 | g0011 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0005 | EUR | IBS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0005 | EUR | IBS | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01884 | hp1 | a0001 | c0012 | t0001 | g0028 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01891 | hp1 | a0005 | c0004 | t0001 | g0013 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01978 | hp1 | a0005 | c0004 | t0001 | g0010 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01981 | hp2 | a0001 | c0012 | t0001 | g0055 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02040 | hp2 | a0001 | c0006 | t0001 | g0017 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02055 | hp1 | a0005 | c0004 | t0001 | g0013 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02071 | hp1 | a0001 | c0024 | t0001 | g0001 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02083 | hp2 | a0012 | c0014 | t0001 | g0047 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02132 | hp1 | a0001 | c0006 | t0001 | g0017 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02132 | hp2 | a0005 | c0004 | t0001 | g0010 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02145 | hp1 | a0004 | c0005 | t0001 | g0015 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02145 | hp2 | a0003 | c0013 | t0001 | g0025 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | CDX | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02258 | hp1 | a0004 | c0005 | t0001 | g0015 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02258 | hp2 | a0006 | c0007 | t0001 | g0018 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02280 | hp2 | a0005 | c0004 | t0001 | g0013 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02293 | hp1 | a0005 | c0004 | t0001 | g0010 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0017 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02451 | hp2 | a0006 | c0007 | t0001 | g0018 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02523 | hp1 | a0001 | c0006 | t0001 | g0017 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0072 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02572 | hp2 | a0006 | c0007 | t0001 | g0018 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02615 | hp1 | a0005 | c0004 | t0001 | g0013 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02615 | hp2 | a0001 | c0006 | t0001 | g0017 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0068 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02647 | hp2 | a0001 | c0006 | t0001 | g0017 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02717 | hp1 | a0005 | c0004 | t0001 | g0022 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02723 | hp1 | a0008 | c0011 | t0001 | g0001 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02735 | hp2 | a0001 | c0006 | t0001 | g0023 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02738 | hp1 | a0004 | c0009 | t0001 | g0011 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02809 | hp1 | a0008 | c0011 | t0001 | g0001 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02886 | hp1 | a0001 | c0012 | t0001 | g0028 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02896 | hp1 | a0004 | c0005 | t0001 | g0021 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02897 | hp2 | a0004 | c0005 | t0001 | g0021 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02922 | hp1 | a0005 | c0004 | t0001 | g0013 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0069 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02965 | hp1 | a0005 | c0004 | t0001 | g0013 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02970 | hp1 | a0005 | c0004 | t0001 | g0013 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02970 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02976 | hp1 | a0005 | c0004 | t0001 | g0066 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02976 | hp2 | a0004 | c0005 | t0001 | g0035 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03017 | hp2 | a0002 | c0008 | t0001 | g0002 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03098 | hp1 | a0005 | c0004 | t0001 | g0013 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0041 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03130 | hp1 | a0014 | c0026 | t0001 | g0003 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0014 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0037 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03209 | hp2 | a0001 | c0006 | t0001 | g0040 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03225 | hp1 | a0003 | c0013 | t0001 | g0025 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03239 | hp2 | a0004 | c0005 | t0001 | g0034 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0014 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03486 | hp2 | a0001 | c0006 | t0001 | g0014 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03490 | hp2 | a0002 | c0008 | t0001 | g0002 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03491 | hp2 | a0004 | c0009 | t0001 | g0011 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03492 | hp1 | a0002 | c0008 | t0001 | g0002 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03492 | hp2 | a0004 | c0009 | t0001 | g0011 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | ESN | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03540 | hp1 | a0006 | c0007 | t0001 | g0018 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03579 | hp1 | a0001 | c0006 | t0001 | g0014 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03579 | hp2 | a0005 | c0004 | t0001 | g0022 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03654 | hp1 | a0005 | c0004 | t0001 | g0010 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03654 | hp2 | a0004 | c0009 | t0001 | g0011 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03669 | hp1 | a0004 | c0005 | t0001 | g0015 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03710 | hp1 | a0004 | c0005 | t0001 | g0015 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03831 | hp2 | a0002 | c0008 | t0001 | g0060 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03834 | hp1 | a0004 | c0005 | t0001 | g0036 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03927 | hp1 | a0004 | c0005 | t0001 | g0034 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03927 | hp2 | a0002 | c0008 | t0001 | g0002 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03942 | hp1 | a0015 | c0020 | t0001 | g0001 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG04184 | hp1 | a0001 | c0006 | t0001 | g0023 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0008 | SAS | STU | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | STU | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG04228 | hp2 | a0001 | c0006 | t0001 | g0023 | SAS | STU | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0014 | AFR | YRI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | YRI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18612 | hp1 | a0005 | c0004 | t0001 | g0010 | EAS | CHB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | YRI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18906 | hp2 | a0001 | c0006 | t0001 | g0014 | AFR | YRI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18945 | hp1 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18945 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18946 | hp2 | a0005 | c0004 | t0001 | g0010 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18948 | hp2 | a0004 | c0005 | t0001 | g0021 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18963 | hp1 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18964 | hp2 | a0007 | c0021 | t0001 | g0026 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18967 | hp2 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18968 | hp1 | a0016 | c0016 | t0001 | g0050 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18977 | hp2 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18979 | hp2 | a0017 | c0023 | t0001 | g0045 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18980 | hp2 | a0005 | c0004 | t0001 | g0064 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18985 | hp2 | a0004 | c0005 | t0001 | g0015 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18986 | hp2 | a0005 | c0004 | t0001 | g0010 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18988 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18990 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA18999 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19011 | hp2 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | LWK | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19030 | hp2 | a0018 | c0022 | t0001 | g0039 | AFR | LWK | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19054 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19055 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19056 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19057 | hp1 | a0005 | c0004 | t0001 | g0010 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19078 | hp2 | a0005 | c0004 | t0001 | g0010 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19079 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19083 | hp2 | a0003 | c0003 | t0001 | g0070 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19087 | hp2 | a0019 | c0025 | t0001 | g0007 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19240 | hp1 | a0003 | c0015 | t0001 | g0003 | AFR | YRI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA19240 | hp2 | a0008 | c0011 | t0001 | g0001 | AFR | YRI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20129 | hp2 | a0004 | c0005 | t0001 | g0011 | AFR | ASW | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20752 | hp1 | a0004 | c0005 | t0001 | g0021 | EUR | TSI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0020 | EUR | TSI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | TSI | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | GIH | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01123 | hp1 | a0011 | c0027 | t0001 | g0002 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG01123 | hp2 | a0004 | c0005 | t0001 | g0015 | AMR | CLM | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02109 | hp2 | a0013 | c0018 | t0001 | g0063 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02486 | hp1 | a0005 | c0004 | t0001 | g0013 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0014 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG02559 | hp2 | a0004 | c0005 | t0001 | g0015 | AFR | ACB | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03471 | hp1 | a0006 | c0007 | t0001 | g0018 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG03471 | hp2 | a0005 | c0004 | t0001 | g0013 | AFR | MSL | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | USA | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| HG06807 | hp2 | a0006 | c0007 | t0001 | g0018 | AFR | USA | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | USA | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0025 | AFR | USA | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA21309 | hp1 | a0004 | c0005 | t0001 | g0011 | AFR | LWK | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | LWK | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0056 | REF | REF | VARS2_chr6_30909238_30931459 | VARS2 | chr6 | 30909238 | 30931459 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30914912 | C | T | 1 | a0005 | 27 | HG00609.hp2 HG00673.hp2 HG00735.hp1 others(24): Show |
missense_variant | MODERATE | c.76C>T | p.His26Tyr | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 2/30 | 210/3575 | 76/3192 | 26/1063 | chr6 | 30914912 | |||
| chr6:30915026 | G | A | 1 | a0005 | 27 | HG00609.hp2 HG00673.hp2 HG00735.hp1 others(24): Show |
missense_variant | MODERATE | c.190G>A | p.Gly64Arg | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 2/30 | 324/3575 | 190/3192 | 64/1063 | chr6 | 30915026 | |||
| chr6:30915790 | C | G | 1 | a0014 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.429C>G | p.Ile143Met | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 5/30 | 563/3575 | 429/3192 | 143/1063 | chr6 | 30915790 | |||
| chr6:30916185 | G | A | 1 | a0008 | 3 | HG02723.hp1 HG02809.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.607G>A | p.Gly203Arg | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/30 | 741/3575 | 607/3192 | 203/1063 | chr6 | 30916185 | |||
| chr6:30916942 | T | C | 1 | a0012 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.736T>C | p.Cys246Arg | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 8/30 | 870/3575 | 736/3192 | 246/1063 | chr6 | 30916942 | |||
| chr6:30916948 | A | C | 1 | a0019 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.742A>C | p.Thr248Pro | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 8/30 | 876/3575 | 742/3192 | 248/1063 | chr6 | 30916948 | |||
| chr6:30917703 | C | A | 1 | a0016 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.882C>A | p.Asn294Lys | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/30 | 1016/3575 | 882/3192 | 294/1063 | chr6 | 30917703 | |||
| chr6:30920342 | C | T | 1 | a0017 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.1303C>T | p.Arg435Trp | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 14/30 | 1437/3575 | 1303/3192 | 435/1063 | chr6 | 30920342 | |||
| chr6:30920384 | T | C | 12 | a0001 a0002 a0006 others(9): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
missense_variant | MODERATE | c.1345T>C | p.Trp449Arg | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 14/30 | 1479/3575 | 1345/3192 | 449/1063 | chr6 | 30920384 | |||
| chr6:30921099 | C | T | 1 | a0006 | 6 | HG02258.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.1514C>T | p.Ser505Phe | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 16/30 | 1648/3575 | 1514/3192 | 505/1063 | chr6 | 30921099 | |||
| chr6:30921626 | C | A | 1 | a0011 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.1670C>A | p.Ala557Asp | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 18/30 | 1804/3575 | 1670/3192 | 557/1063 | chr6 | 30921626 | |||
| chr6:30922706 | G | T | 2 | a0002 a0011 |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
missense_variant&splice_region_variant | MODERATE | c.2038G>T | p.Val680Leu | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 22/30 | 2172/3575 | 2038/3192 | 680/1063 | chr6 | 30922706 | |||
| chr6:30922730 | G | A | 1 | a0009 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.2062G>A | p.Gly688Arg | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 22/30 | 2196/3575 | 2062/3192 | 688/1063 | chr6 | 30922730 | |||
| chr6:30922758 | T | C | 1 | a0013 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2090T>C | p.Ile697Thr | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 22/30 | 2224/3575 | 2090/3192 | 697/1063 | chr6 | 30922758 | |||
| chr6:30924387 | C | T | 1 | a0010 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.2500C>T | p.Arg834Cys | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/30 | 2634/3575 | 2500/3192 | 834/1063 | chr6 | 30924387 | |||
| chr6:30925304 | C | T | 1 | a0007 | 4 | NA18945.hp1 NA18963.hp1 NA18967.hp2 others(1): Show |
missense_variant | MODERATE | c.2704C>T | p.Arg902Cys | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 27/30 | 2838/3575 | 2704/3192 | 902/1063 | chr6 | 30925304 | |||
| chr6:30925305 | G | T | 1 | a0007 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.2705G>T | p.Arg902Leu | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 27/30 | 2839/3575 | 2705/3192 | 902/1063 | chr6 | 30925305 | |||
| chr6:30925328 | G | A | 1 | a0018 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2728G>A | p.Val910Met | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 27/30 | 2862/3575 | 2728/3192 | 910/1063 | chr6 | 30925328 | |||
| chr6:30925350 | G | A | 10 | a0001 a0006 a0007 others(7): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
missense_variant | MODERATE | c.2750G>A | p.Arg917Gln | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 27/30 | 2884/3575 | 2750/3192 | 917/1063 | chr6 | 30925350 | |||
| chr6:30925651 | G | A | 3 | a0002 a0011 a0015 |
91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
missense_variant | MODERATE | c.2893G>A | p.Ala965Thr | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 28/30 | 3027/3575 | 2893/3192 | 965/1063 | chr6 | 30925651 | |||
| chr6:30926164 | G | A | 1 | a0004 | 29 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(26): Show |
missense_variant | MODERATE | c.3146G>A | p.Arg1049Gln | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 30/30 | 3280/3575 | 3146/3192 | 1049/1063 | chr6 | 30926164 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30914857 | C | T | 4 | a0002c0002 a0002c0008 a0002c0028 others(1): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
synonymous_variant | LOW | c.21C>T | p.Ala7Ala | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 2/30 | 155/3575 | 21/3192 | 7/1063 | chr6 | 30914857 | |||
| chr6:30915004 | G | T | 4 | a0002c0002 a0002c0008 a0002c0028 others(1): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
synonymous_variant | LOW | c.168G>T | p.Ala56Ala | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 2/30 | 302/3575 | 168/3192 | 56/1063 | chr6 | 30915004 | |||
| chr6:30917215 | G | A | 1 | a0003c0015 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.864G>A | p.Ser288Ser | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 9/30 | 998/3575 | 864/3192 | 288/1063 | chr6 | 30917215 | |||
| chr6:30917697 | G | A | 1 | a0001c0012 | 3 | HG01884.hp1 HG01981.hp2 HG02886.hp1 |
splice_region_variant&synonymous_variant | LOW | c.876G>A | p.Val292Val | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/30 | 1010/3575 | 876/3192 | 292/1063 | chr6 | 30917697 | |||
| chr6:30918906 | G | A | 1 | a0003c0013 | 2 | HG02145.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.1065G>A | p.Ser355Ser | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/30 | 1199/3575 | 1065/3192 | 355/1063 | chr6 | 30918906 | |||
| chr6:30919766 | C | T | 1 | a0001c0024 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1083C>T | p.His361His | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 12/30 | 1217/3575 | 1083/3192 | 361/1063 | chr6 | 30919766 | |||
| chr6:30920195 | C | T | 14 | a0001c0001 a0001c0006 a0001c0012 others(11): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
synonymous_variant | LOW | c.1272C>T | p.Ser424Ser | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 13/30 | 1406/3575 | 1272/3192 | 424/1063 | chr6 | 30920195 | |||
| chr6:30920211 | C | T | 4 | a0002c0002 a0002c0008 a0002c0028 others(1): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
synonymous_variant | LOW | c.1288C>T | p.Leu430Leu | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 13/30 | 1422/3575 | 1288/3192 | 430/1063 | chr6 | 30920211 | |||
| chr6:30920392 | G | A | 4 | a0002c0002 a0002c0008 a0002c0028 others(1): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
synonymous_variant | LOW | c.1353G>A | p.Leu451Leu | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 14/30 | 1487/3575 | 1353/3192 | 451/1063 | chr6 | 30920392 | |||
| chr6:30921612 | T | C | 12 | a0001c0001 a0001c0024 a0002c0008 others(9): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
synonymous_variant | LOW | c.1656T>C | p.Val552Val | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 18/30 | 1790/3575 | 1656/3192 | 552/1063 | chr6 | 30921612 | |||
| chr6:30923367 | C | T | 1 | a0004c0009 | 4 | HG02738.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
synonymous_variant | LOW | c.2328C>T | p.Ser776Ser | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/30 | 2462/3575 | 2328/3192 | 776/1063 | chr6 | 30923367 | |||
| chr6:30923451 | C | T | 2 | a0002c0028 a0006c0007 |
7 | HG00639.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
synonymous_variant | LOW | c.2412C>T | p.Leu804Leu | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/30 | 2546/3575 | 2412/3192 | 804/1063 | chr6 | 30923451 | |||
| chr6:30924465 | C | T | 1 | a0006c0007 | 6 | HG02258.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.2578C>T | p.Leu860Leu | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/30 | 2712/3575 | 2578/3192 | 860/1063 | chr6 | 30924465 | |||
| chr6:30924545 | C | T | 4 | a0002c0002 a0002c0008 a0002c0028 others(1): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
synonymous_variant | LOW | c.2658C>T | p.Pro886Pro | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/30 | 2792/3575 | 2658/3192 | 886/1063 | chr6 | 30924545 | |||
| chr6:30925951 | C | T | 21 | a0001c0001 a0001c0006 a0001c0012 others(18): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
synonymous_variant | LOW | c.3033C>T | p.Asp1011Asp | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 29/30 | 3167/3575 | 3033/3192 | 1011/1063 | chr6 | 30925951 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30926404 | C | T | 1 | a0001c0001t0002 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*194C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 30/30 | 194 | chr6 | 30926404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30914426 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.-28+82T>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 1/29 | chr6 | 30914426 | |||||||
| chr6:30914500 | C | T | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-28+156C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 1/29 | chr6 | 30914500 | |||||||
| chr6:30914638 | C | T | 2 | a0004c0005t0001g0011 a0004c0009t0001g0011 |
11 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.-27-172C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 1/29 | chr6 | 30914638 | |||||||
| chr6:30914654 | C | T | 1 | a0005c0004t0001g0013 | 10 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-27-156C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 1/29 | chr6 | 30914654 | |||||||
| chr6:30914736 | A | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-27-74A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 1/29 | chr6 | 30914736 | |||||||
| chr6:30915079 | A | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.201+42A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 2/29 | chr6 | 30915079 | |||||||
| chr6:30915266 | C | T | 1 | a0003c0003t0001g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.283+29C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 3/29 | chr6 | 30915266 | |||||||
| chr6:30915284 | C | G | 1 | a0001c0001t0001g0029 | 2 | NA18970.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.283+47C>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 3/29 | chr6 | 30915284 | |||||||
| chr6:30916101 | AAAGCAAC others(1): Show |
A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(66): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.574-42_574-35delAA others(6): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr6 | 30916101 | ||||||
| chr6:30916109 | C | A | 1 | a0002c0002t0001g0057 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.574-43C>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 6/29 | chr6 | 30916109 | |||||||
| chr6:30916125 | G | T | 2 | a0001c0012t0001g0028 a0001c0012t0001g0055 |
3 | HG01884.hp1 HG01981.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.574-27G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 6/29 | chr6 | 30916125 | |||||||
| chr6:30916143 | C | T | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.574-9C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 6/29 | chr6 | 30916143 | |||||||
| chr6:30916410 | C | T | 1 | a0002c0002t0001g0062 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.671+161C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916410 | |||||||
| chr6:30916423 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.671+174G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916423 | |||||||
| chr6:30916453 | C | CGT | 5 | a0003c0003t0001g0005 a0003c0003t0001g0025 a0003c0003t0001g0072 others(2): Show |
26 | HG01099.hp1 HG01106.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.671+227_671+228dup others(2): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916453 | ||||||
| chr6:30916453 | C | CGTGT | 2 | a0001c0001t0001g0052 a0003c0003t0001g0016 |
8 | HG01175.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.671+225_671+228dup others(4): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916453 | ||||||
| chr6:30916453 | CGT | C | 2 | a0003c0003t0001g0032 a0013c0018t0001g0063 |
3 | HG00642.hp1 HG01081.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.671+227_671+228del others(2): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916453 | ||||||
| chr6:30916465 | T | TGTGG | 12 | a0001c0006t0001g0014 a0001c0006t0001g0017 a0001c0006t0001g0023 others(9): Show |
30 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+219_671+220ins others(4): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916465 | ||||||
| chr6:30916474 | G | A | 11 | a0002c0002t0001g0002 a0002c0002t0001g0020 a0002c0002t0001g0030 others(8): Show |
68 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.671+225G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916474 | |||||||
| chr6:30916476 | G | A | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.671+227G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916476 | |||||||
| chr6:30916476 | G | GTGTATT | 17 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0024 others(14): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.671+228_671+229ins others(6): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916476 | ||||||
| chr6:30916476 | G | GTGTGTAT others(1): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0002g0009 others(1): Show |
16 | HG01167.hp2 HG01168.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.671+228_671+229ins others(8): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916476 | ||||||
| chr6:30916476 | G | GTGTGTAT others(3): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0029 |
8 | NA18942.hp2 NA18960.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.671+228_671+229ins others(10): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916476 | ||||||
| chr6:30916476 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0054 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.671+228_671+229ins others(10): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916476 | ||||||
| chr6:30916476 | G | GTGTGTGT others(5): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0053 |
21 | HG00423.hp1 HG00423.hp2 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.671+228_671+229ins others(12): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916476 | ||||||
| chr6:30916478 | A | ATT | 2 | a0002c0002t0001g0004 a0002c0002t0001g0057 |
21 | HG00642.hp2 HG01361.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.671+231_671+232dup others(2): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916478 | ||||||
| chr6:30916478 | A | T | 11 | a0002c0002t0001g0002 a0002c0002t0001g0020 a0002c0002t0001g0030 others(8): Show |
68 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.671+229A>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916478 | |||||||
| chr6:30916480 | T | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(24): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.671+231T>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916480 | |||||||
| chr6:30916480 | T | TTA | 1 | a0005c0004t0001g0022 | 4 | HG00735.hp1 HG01106.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+247_671+248dup others(2): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916480 | ||||||
| chr6:30916480 | T | TTATA | 11 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0006t0001g0014 others(8): Show |
38 | HG01109.hp1 HG01243.hp2 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.671+245_671+248dup others(4): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916480 | ||||||
| chr6:30916480 | T | TTATATA | 2 | a0001c0006t0001g0037 a0001c0012t0001g0028 |
3 | HG01884.hp1 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.671+243_671+248dup others(6): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916480 | ||||||
| chr6:30916480 | T | TTATATAT others(1): Show |
2 | a0004c0005t0001g0021 a0004c0005t0001g0036 |
5 | HG02896.hp1 HG02897.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+241_671+248dup others(8): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr6 | 30916480 | ||||||
| chr6:30916496 | A | T | 1 | a0004c0005t0001g0035 | 2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.671+247A>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916496 | |||||||
| chr6:30916498 | T | A | 1 | a0005c0004t0001g0064 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.671+249T>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916498 | |||||||
| chr6:30916519 | C | T | 1 | a0001c0012t0001g0028 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.671+270C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916519 | |||||||
| chr6:30916554 | CG | C | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.671+306delG | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916554 | |||||||
| chr6:30916659 | A | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.672-219A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 7/29 | chr6 | 30916659 | |||||||
| chr6:30917025 | G | A | 1 | a0003c0003t0001g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.753+66G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 8/29 | chr6 | 30917025 | |||||||
| chr6:30917026 | A | G | 1 | a0003c0003t0001g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.753+67A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 8/29 | chr6 | 30917026 | |||||||
| chr6:30917028 | G | A | 1 | a0003c0003t0001g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.753+69G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 8/29 | chr6 | 30917028 | |||||||
| chr6:30917029 | A | C | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.753+70A>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 8/29 | chr6 | 30917029 | |||||||
| chr6:30917862 | A | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.985+56A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30917862 | |||||||
| chr6:30917909 | T | A | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.985+103T>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30917909 | |||||||
| chr6:30918010 | T | A | 1 | a0016c0016t0001g0050 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.985+204T>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918010 | |||||||
| chr6:30918044 | G | A | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.985+238G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918044 | |||||||
| chr6:30918062 | TTTTG | T | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.985+276_985+279del others(4): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr6 | 30918062 | ||||||
| chr6:30918138 | G | C | 1 | a0016c0016t0001g0050 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.985+332G>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918138 | |||||||
| chr6:30918213 | G | A | 1 | a0004c0005t0001g0065 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.985+407G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918213 | |||||||
| chr6:30918238 | T | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.985+432T>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918238 | |||||||
| chr6:30918302 | G | A | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.985+496G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918302 | |||||||
| chr6:30918313 | G | T | 1 | a0004c0005t0001g0035 | 2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.985+507G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918313 | |||||||
| chr6:30918320 | C | A | 2 | a0004c0005t0001g0021 a0004c0005t0001g0036 |
5 | HG02896.hp1 HG02897.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.986-507C>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918320 | |||||||
| chr6:30918341 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(28): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.986-486C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918341 | |||||||
| chr6:30918360 | C | G | 1 | a0001c0006t0001g0014 | 8 | HG01243.hp2 HG02486.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.986-467C>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918360 | |||||||
| chr6:30918385 | G | A | 1 | a0013c0018t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.986-442G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918385 | |||||||
| chr6:30918453 | G | T | 1 | a0009c0017t0001g0071 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.986-374G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918453 | |||||||
| chr6:30918463 | G | GTGCTCCC others(18): Show |
1 | a0003c0003t0001g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.986-362_986-338dup others(25): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr6 | 30918463 | ||||||
| chr6:30918573 | C | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.986-254C>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918573 | |||||||
| chr6:30918653 | AACCCTGG others(133): Show |
A | 4 | a0004c0005t0001g0011 a0004c0005t0001g0021 a0004c0005t0001g0036 others(1): Show |
16 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.986-170_986-31del | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr6 | 30918653 | ||||||
| chr6:30918774 | A | C | 1 | a0001c0001t0001g0006 | 2 | NA19058.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.986-53A>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 10/29 | chr6 | 30918774 | |||||||
| chr6:30918947 | C | T | 1 | a0006c0007t0001g0018 | 6 | HG02258.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074+32C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30918947 | |||||||
| chr6:30918952 | C | T | 2 | a0002c0002t0001g0020 a0002c0002t0001g0058 |
6 | HG00280.hp1 HG01099.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+37C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30918952 | |||||||
| chr6:30918953 | G | A | 1 | a0001c0006t0001g0038 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1074+38G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30918953 | |||||||
| chr6:30918957 | A | T | 1 | a0003c0003t0001g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1074+42A>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30918957 | |||||||
| chr6:30919150 | G | C | 3 | a0001c0006t0001g0014 a0001c0006t0001g0023 a0001c0006t0001g0038 |
12 | HG01243.hp2 HG01361.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1074+235G>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919150 | |||||||
| chr6:30919186 | T | C | 1 | a0004c0005t0001g0035 | 2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1074+271T>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919186 | |||||||
| chr6:30919203 | C | T | 1 | a0002c0002t0001g0031 | 2 | NA19083.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1074+288C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919203 | |||||||
| chr6:30919271 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1074+356C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919271 | |||||||
| chr6:30919272 | G | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0027 others(3): Show |
30 | HG00423.hp1 HG00423.hp2 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.1074+357G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919272 | |||||||
| chr6:30919331 | TTTTTTAA others(9): Show |
T | 1 | a0003c0003t0001g0016 | 7 | HG01175.hp1 HG01891.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-412_1075-397d others(18): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr6 | 30919331 | ||||||
| chr6:30919430 | C | T | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1075-328C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919430 | |||||||
| chr6:30919465 | G | A | 4 | a0005c0004t0001g0010 a0005c0004t0001g0013 a0005c0004t0001g0064 others(1): Show |
23 | HG00609.hp2 HG00673.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1075-293G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919465 | |||||||
| chr6:30919477 | G | C | 1 | a0003c0003t0001g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1075-281G>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919477 | |||||||
| chr6:30919478 | C | G | 1 | a0003c0003t0001g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1075-280C>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919478 | |||||||
| chr6:30919534 | C | T | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1075-224C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919534 | |||||||
| chr6:30919567 | T | C | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1075-191T>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919567 | |||||||
| chr6:30919688 | C | T | 2 | a0005c0004t0001g0010 a0005c0004t0001g0064 |
12 | HG00609.hp2 HG00673.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1075-70C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 11/29 | chr6 | 30919688 | |||||||
| chr6:30919996 | G | A | 1 | a0003c0003t0001g0032 | 2 | HG00642.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1166-93G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 12/29 | chr6 | 30919996 | |||||||
| chr6:30920003 | C | CTGGGGCG others(10): Show |
55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1166-83_1166-67dup others(17): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr6 | 30920003 | ||||||
| chr6:30920084 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG03516.hp1 | splice_region_variant&intron_variant | LOW | c.1166-5C>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 12/29 | chr6 | 30920084 | |||||||
| chr6:30920261 | C | T | 1 | a0001c0012t0001g0028 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1293+45C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 13/29 | chr6 | 30920261 | |||||||
| chr6:30920561 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0027 others(3): Show |
30 | HG00423.hp1 HG00423.hp2 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.1398-107G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 14/29 | chr6 | 30920561 | |||||||
| chr6:30920561 | G | T | 1 | a0003c0003t0001g0032 | 2 | HG00642.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1398-107G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 14/29 | chr6 | 30920561 | |||||||
| chr6:30920590 | G | A | 1 | a0018c0022t0001g0039 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1398-78G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 14/29 | chr6 | 30920590 | |||||||
| chr6:30920600 | G | A | 1 | a0005c0004t0001g0022 | 4 | HG00735.hp1 HG01106.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-68G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 14/29 | chr6 | 30920600 | |||||||
| chr6:30920840 | G | A | 3 | a0004c0005t0001g0015 a0004c0005t0001g0035 a0004c0005t0001g0065 |
11 | HG00323.hp1 HG00323.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1479+91G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 15/29 | chr6 | 30920840 | |||||||
| chr6:30921035 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1480-30A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 15/29 | chr6 | 30921035 | |||||||
| chr6:30921056 | T | C | 2 | a0003c0003t0001g0025 a0003c0013t0001g0025 |
3 | HG02145.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1480-9T>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 15/29 | chr6 | 30921056 | |||||||
| chr6:30921343 | A | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1632+38A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 17/29 | chr6 | 30921343 | |||||||
| chr6:30921389 | G | T | 1 | a0001c0001t0001g0027 | 2 | HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1632+84G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 17/29 | chr6 | 30921389 | |||||||
| chr6:30921415 | C | T | 1 | a0001c0006t0001g0041 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1632+110C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 17/29 | chr6 | 30921415 | |||||||
| chr6:30921437 | C | T | 1 | a0004c0005t0001g0036 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1632+132C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 17/29 | chr6 | 30921437 | |||||||
| chr6:30921483 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1633-106G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 17/29 | chr6 | 30921483 | |||||||
| chr6:30921518 | G | A | 2 | a0001c0006t0001g0040 a0001c0006t0001g0041 |
2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1633-71G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 17/29 | chr6 | 30921518 | |||||||
| chr6:30921712 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1735+21G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 18/29 | chr6 | 30921712 | |||||||
| chr6:30922039 | G | T | 1 | a0002c0002t0001g0030 | 2 | HG02155.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1806+44G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 19/29 | chr6 | 30922039 | |||||||
| chr6:30922067 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1807-49T>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 19/29 | chr6 | 30922067 | |||||||
| chr6:30922278 | T | C | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1932+37T>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 20/29 | chr6 | 30922278 | |||||||
| chr6:30922381 | G | A | 1 | a0010c0019t0001g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1933-69G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 20/29 | chr6 | 30922381 | |||||||
| chr6:30922418 | A | C | 1 | a0004c0005t0001g0034 | 2 | HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1933-32A>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 20/29 | chr6 | 30922418 | |||||||
| chr6:30922418 | A | G | 3 | a0004c0005t0001g0015 a0004c0005t0001g0035 a0004c0005t0001g0065 |
11 | HG00323.hp1 HG00323.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1933-32A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 20/29 | chr6 | 30922418 | |||||||
| chr6:30922429 | T | C | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1933-21T>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 20/29 | chr6 | 30922429 | |||||||
| chr6:30922654 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2038-52A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 21/29 | chr6 | 30922654 | |||||||
| chr6:30922792 | G | T | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2106+18G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 22/29 | chr6 | 30922792 | |||||||
| chr6:30923012 | G | A | 3 | a0004c0005t0001g0015 a0004c0005t0001g0035 a0004c0005t0001g0065 |
11 | HG00323.hp1 HG00323.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2185+36G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 23/29 | chr6 | 30923012 | |||||||
| chr6:30923017 | C | T | 1 | a0003c0003t0001g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2185+41C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 23/29 | chr6 | 30923017 | |||||||
| chr6:30923022 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2185+46A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 23/29 | chr6 | 30923022 | |||||||
| chr6:30923094 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.2186-10T>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 23/29 | chr6 | 30923094 | |||||||
| chr6:30923633 | C | T | 1 | a0004c0005t0001g0034 | 2 | HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2466+128C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | chr6 | 30923633 | |||||||
| chr6:30923671 | TG | T | 10 | a0001c0006t0001g0014 a0001c0006t0001g0017 a0001c0006t0001g0023 others(7): Show |
25 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.2466+168delG | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr6 | 30923671 | ||||||
| chr6:30923673 | G | C | 10 | a0001c0006t0001g0014 a0001c0006t0001g0017 a0001c0006t0001g0023 others(7): Show |
25 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.2466+168G>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | chr6 | 30923673 | |||||||
| chr6:30923918 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(67): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2466+413G>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | chr6 | 30923918 | |||||||
| chr6:30923918 | G | T | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2466+413G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | chr6 | 30923918 | |||||||
| chr6:30923925 | C | T | 1 | a0013c0018t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2466+420C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | chr6 | 30923925 | |||||||
| chr6:30923927 | C | CCG | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2466+423_2466+424i others(4): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr6 | 30923927 | ||||||
| chr6:30924018 | G | GTGC | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2467-324_2467-322d others(5): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr6 | 30924018 | ||||||
| chr6:30924077 | C | G | 1 | a0001c0012t0001g0028 | 2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2467-277C>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | chr6 | 30924077 | |||||||
| chr6:30924277 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2467-77A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | chr6 | 30924277 | |||||||
| chr6:30924282 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0007c0021t0001g0026 others(1): Show |
17 | HG01109.hp1 HG01192.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.2467-72C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | chr6 | 30924282 | |||||||
| chr6:30924292 | TGGCTGTA others(7): Show |
T | 1 | a0002c0008t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2467-59_2467-46del others(14): Show |
VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr6 | 30924292 | ||||||
| chr6:30924335 | C | T | 1 | a0004c0005t0001g0035 | 2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2467-19C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 25/29 | chr6 | 30924335 | |||||||
| chr6:30924600 | G | C | 13 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(10): Show |
89 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.2673+40G>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924600 | |||||||
| chr6:30924601 | G | C | 1 | a0002c0008t0001g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2673+41G>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924601 | |||||||
| chr6:30924691 | T | G | 1 | a0002c0002t0001g0059 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2673+131T>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924691 | |||||||
| chr6:30924692 | G | T | 1 | a0002c0002t0001g0059 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2673+132G>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924692 | |||||||
| chr6:30924693 | T | G | 1 | a0002c0002t0001g0059 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2673+133T>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924693 | |||||||
| chr6:30924710 | C | T | 1 | a0003c0003t0001g0069 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2673+150C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924710 | |||||||
| chr6:30924744 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(57): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2673+184G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924744 | |||||||
| chr6:30924815 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2673+255G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924815 | |||||||
| chr6:30924815 | G | C | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2673+255G>C | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924815 | |||||||
| chr6:30924940 | A | G | 1 | a0004c0005t0001g0035 | 2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2674-334A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924940 | |||||||
| chr6:30924943 | T | G | 1 | a0017c0023t0001g0045 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2674-331T>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924943 | |||||||
| chr6:30924946 | C | G | 1 | a0001c0001t0001g0048 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2674-328C>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924946 | |||||||
| chr6:30924986 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2674-288T>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30924986 | |||||||
| chr6:30925220 | G | A | 1 | a0003c0003t0001g0032 | 2 | HG00642.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2674-54G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30925220 | |||||||
| chr6:30925222 | AC | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(38): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.2674-51delC | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 26/29 | chr6 | 30925222 | |||||||
| chr6:30925449 | C | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2785+64C>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 27/29 | chr6 | 30925449 | |||||||
| chr6:30925474 | G | A | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2786-70G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 27/29 | chr6 | 30925474 | |||||||
| chr6:30925785 | TG | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0054 |
11 | HG00140.hp1 HG00558.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.2961+69delG | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr6 | 30925785 | ||||||
| chr6:30925818 | A | G | 1 | a0003c0003t0001g0033 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2962-62A>G | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 28/29 | chr6 | 30925818 | |||||||
| chr6:30926054 | G | A | 14 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0020 others(11): Show |
90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.3090+46G>A | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 29/29 | chr6 | 30926054 | |||||||
| chr6:30926099 | C | T | 2 | a0003c0003t0001g0068 a0012c0014t0001g0047 |
2 | HG02083.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3091-10C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 29/29 | chr6 | 30926099 | |||||||
| chr6:30926106 | C | T | 1 | a0001c0001t0001g0024 | 3 | NA18941.hp2 NA18995.hp2 NA19088.hp1 |
splice_region_variant&intron_variant | LOW | c.3091-3C>T | VARS2 | ENSG00000137411.19 | transcript | ENST00000676266.1 | protein_coding | 29/29 | chr6 | 30926106 |