Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 220001 |
| ensemblid | ENSG00000167992.14 |
| hgncid | 26487 |
| symbol | VWCE |
| name | von Willebrand factor C and EGF domains |
| refseq_nuc | NM_152718.2 |
| refseq_prot | NP_689931.2 |
| ensembl_nuc | ENST00000335613.10 |
| ensembl_prot | ENSP00000334186.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 61258286 |
| end | 61295316 |
| strand | - |
| ver | v1.2 |
| region | chr11:61258286-61295316 |
| region5000 | chr11:61253286-61300316 |
| regionname0 | VWCE_chr11_61258286_61295316 |
| regionname5000 | VWCE_chr11_61253286_61300316 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 955 | 162 | 72 | 27 | 36 | 10 | 15 | 12 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0002 | 0/0 | 955 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0003 | 0/0 | 955 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0004 | 0/0 | 955 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0005 | 0/0 | 955 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0006 | 0/0 | 955 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0007 | 0/0 | 955 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0008 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0009 | 0/0 | 955 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0010 | 0/0 | 955 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0011 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0012 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0013 | 0/0 | 955 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| a0014 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | MWAGL others(950): Show |
chr11 | 61253286 | 61300316 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2865 | 118 | 35 | 24 | 34 | 10 | 13 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0001c0002 | 0/0 | 2865 | 16 | 14 | 1 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0001c0003 | 0/0 | 2865 | 7 | 5 | 1 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0001c0004 | 0/0 | 2865 | 7 | 6 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0001c0006 | 0/0 | 2865 | 6 | 6 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0001c0012 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0001c0013 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0001c0014 | 0/0 | 2865 | 2 | 0 | 0 | 2 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0001c0021 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0001c0024 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0002c0005 | 0/0 | 2865 | 6 | 0 | 0 | 6 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0003c0007 | 0/0 | 2865 | 4 | 4 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0003c0010 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0004c0008 | 0/0 | 2865 | 3 | 0 | 3 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0005c0015 | 0/0 | 2865 | 2 | 0 | 0 | 2 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0006c0009 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0007c0011 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0008c0023 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0009c0020 | 0/0 | 2865 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0010c0022 | 0/0 | 2865 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0011c0018 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0012c0016 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0013c0019 | 0/0 | 2865 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 | ||
| a0014c0017 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | ATGTG others(2860): Show |
chr11 | 61253286 | 61300316 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3536 | 113 | 32 | 24 | 33 | 10 | 12 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0001t0002 | 0/0 | 3521 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3516): Show |
chr11 | 61253286 | 61300316 |
| a0001c0001t0003 | 0/0 | 3536 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0001t0004 | 0/0 | 3536 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0001t0005 | 0/0 | 3536 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0001t0006 | 0/0 | 3536 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0002t0001 | 0/0 | 3536 | 15 | 13 | 1 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0002t0007 | 0/0 | 3536 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0003t0001 | 0/0 | 3536 | 7 | 5 | 1 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0004t0001 | 0/0 | 3536 | 7 | 6 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0006t0001 | 0/0 | 3536 | 6 | 6 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0012t0001 | 0/0 | 3536 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0013t0001 | 0/0 | 3536 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0014t0001 | 0/0 | 3536 | 2 | 0 | 0 | 2 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0021t0001 | 0/0 | 3536 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0001c0024t0001 | 0/0 | 3536 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0002c0005t0001 | 0/0 | 3536 | 6 | 0 | 0 | 6 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0003c0007t0001 | 0/0 | 3536 | 4 | 4 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0003c0010t0001 | 0/0 | 3536 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0004c0008t0001 | 0/0 | 3536 | 3 | 0 | 3 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0005c0015t0001 | 0/0 | 3536 | 2 | 0 | 0 | 2 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0006c0009t0001 | 0/0 | 3536 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0007c0011t0001 | 0/0 | 3536 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0008c0023t0001 | 0/0 | 3536 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0009c0020t0001 | 0/0 | 3536 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0010c0022t0001 | 0/0 | 3536 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0011c0018t0001 | 0/0 | 3536 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0012c0016t0002 | 0/0 | 3521 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3516): Show |
chr11 | 61253286 | 61300316 |
| a0013c0019t0001 | 0/0 | 3536 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| a0014c0017t0001 | 0/0 | 3536 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | GCGCC others(3531): Show |
chr11 | 61253286 | 61300316 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 1 | 5 | 4 | 2 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0002 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0004 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0002t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0006t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0006t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0012t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0012t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0013t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0013t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0014t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0014t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0021t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0001c0024t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0002c0005t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0002c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0002c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0002c0005t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0003c0007t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0003c0007t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0003c0007t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0003c0007t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0003c0010t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0003c0010t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0004c0008t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0005c0015t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0005c0015t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0006c0009t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0006c0009t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0007c0011t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0007c0011t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0008c0023t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0009c0020t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0010c0022t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0011c0018t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0012c0016t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0013c0019t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| a0014c0017t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00558 | hp1 | a0008 | c0023 | t0001 | g0130 | EAS | CHS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00597 | hp2 | a0005 | c0015 | t0001 | g0044 | EAS | CHS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01069 | hp1 | a0004 | c0008 | t0001 | g0005 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01070 | hp1 | a0004 | c0008 | t0001 | g0005 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01109 | hp1 | a0009 | c0020 | t0001 | g0093 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0025 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01192 | hp2 | a0004 | c0008 | t0001 | g0005 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0140 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01433 | hp2 | a0010 | c0022 | t0001 | g0090 | AMR | CLM | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0138 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02015 | hp2 | a0011 | c0018 | t0001 | g0144 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02056 | hp2 | a0001 | c0014 | t0001 | g0063 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0148 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02165 | hp2 | a0002 | c0005 | t0001 | g0123 | EAS | CDX | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02257 | hp1 | a0001 | c0006 | t0001 | g0127 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0028 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02451 | hp1 | a0012 | c0016 | t0002 | g0012 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02572 | hp2 | a0001 | c0006 | t0001 | g0126 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02615 | hp1 | a0003 | c0007 | t0001 | g0109 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02615 | hp2 | a0001 | c0013 | t0001 | g0103 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02622 | hp1 | a0001 | c0006 | t0001 | g0128 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02647 | hp2 | a0001 | c0012 | t0001 | g0118 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02717 | hp1 | a0001 | c0006 | t0001 | g0011 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0027 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0011 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02735 | hp1 | a0013 | c0019 | t0001 | g0034 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02809 | hp2 | a0001 | c0013 | t0001 | g0132 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02818 | hp2 | a0006 | c0009 | t0001 | g0151 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02886 | hp1 | a0001 | c0006 | t0001 | g0125 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02895 | hp2 | a0003 | c0007 | t0001 | g0107 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02922 | hp1 | a0003 | c0010 | t0001 | g0035 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02965 | hp1 | a0007 | c0011 | t0001 | g0156 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0029 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02970 | hp1 | a0001 | c0021 | t0001 | g0113 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0145 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03098 | hp1 | a0006 | c0009 | t0001 | g0150 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03098 | hp2 | a0003 | c0010 | t0001 | g0104 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03130 | hp2 | a0001 | c0002 | t0007 | g0159 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03209 | hp1 | a0007 | c0011 | t0001 | g0155 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03209 | hp2 | a0003 | c0007 | t0001 | g0108 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03225 | hp2 | a0003 | c0007 | t0001 | g0111 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0124 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03579 | hp1 | a0014 | c0017 | t0001 | g0110 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03579 | hp2 | a0001 | c0012 | t0001 | g0117 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | STU | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | YRI | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18945 | hp2 | a0001 | c0014 | t0001 | g0062 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18954 | hp2 | a0002 | c0005 | t0001 | g0006 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18966 | hp2 | a0002 | c0005 | t0001 | g0006 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18972 | hp1 | a0002 | c0005 | t0001 | g0143 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19010 | hp1 | a0002 | c0005 | t0001 | g0146 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19010 | hp2 | a0005 | c0015 | t0001 | g0071 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19030 | hp1 | a0001 | c0024 | t0001 | g0095 | AFR | LWK | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | LWK | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19060 | hp1 | a0002 | c0005 | t0001 | g0006 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0030 | AFR | YRI | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ASW | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | MSL | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | USA | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0136 | AFR | USA | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0059 | REF | REF | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0065 | REF | REF | VWCE_chr11_61253286_61300316 | VWCE | chr11 | 61253286 | 61300316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61258787 | C | T | 2 | a0003 a0014 |
7 | HG02615.hp1 HG02895.hp2 HG02922.hp1 others(4): Show |
missense_variant | MODERATE | c.2756G>A | p.Arg919His | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 20/20 | 3035/3536 | 2756/2868 | 919/955 | chr11 | 61258787 | |||
| chr11:61259078 | C | T | 1 | a0009 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2465G>A | p.Gly822Asp | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 20/20 | 2744/3536 | 2465/2868 | 822/955 | chr11 | 61259078 | |||
| chr11:61259168 | G | A | 1 | a0007 | 2 | HG02965.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.2375C>T | p.Ser792Leu | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 20/20 | 2654/3536 | 2375/2868 | 792/955 | chr11 | 61259168 | |||
| chr11:61259240 | C | T | 1 | a0013 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.2303G>A | p.Arg768Gln | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 20/20 | 2582/3536 | 2303/2868 | 768/955 | chr11 | 61259240 | |||
| chr11:61267517 | T | C | 1 | a0010 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1910A>G | p.Tyr637Cys | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/20 | 2189/3536 | 1910/2868 | 637/955 | chr11 | 61267517 | |||
| chr11:61273283 | G | C | 1 | a0002 | 6 | HG02165.hp2 NA18954.hp2 NA18966.hp2 others(3): Show |
missense_variant | MODERATE | c.1615C>G | p.Pro539Ala | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/20 | 1894/3536 | 1615/2868 | 539/955 | chr11 | 61273283 | |||
| chr11:61276658 | G | T | 1 | a0006 | 2 | HG02818.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.1430C>A | p.Ser477Tyr | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/20 | 1709/3536 | 1430/2868 | 477/955 | chr11 | 61276658 | |||
| chr11:61278422 | T | C | 1 | a0008 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.1379A>G | p.Asn460Ser | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/20 | 1658/3536 | 1379/2868 | 460/955 | chr11 | 61278422 | |||
| chr11:61280923 | G | A | 1 | a0004 | 3 | HG01069.hp1 HG01070.hp1 HG01192.hp2 |
missense_variant | MODERATE | c.1100C>T | p.Thr367Ile | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 8/20 | 1379/3536 | 1100/2868 | 367/955 | chr11 | 61280923 | |||
| chr11:61280940 | C | G | 1 | a0011 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1083G>C | p.Gln361His | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 8/20 | 1362/3536 | 1083/2868 | 361/955 | chr11 | 61280940 | |||
| chr11:61281089 | C | T | 1 | a0014 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.934G>A | p.Gly312Arg | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 8/20 | 1213/3536 | 934/2868 | 312/955 | chr11 | 61281089 | |||
| chr11:61281191 | G | A | 1 | a0005 | 2 | HG00597.hp2 NA19010.hp2 |
missense_variant | MODERATE | c.832C>T | p.Arg278Trp | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 8/20 | 1111/3536 | 832/2868 | 278/955 | chr11 | 61281191 | |||
| chr11:61286384 | G | T | 1 | a0012 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.471C>A | p.Asn157Lys | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/20 | 750/3536 | 471/2868 | 157/955 | chr11 | 61286384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61259014 | T | C | 3 | a0001c0021 a0003c0007 a0014c0017 |
6 | HG02615.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
synonymous_variant | LOW | c.2529A>G | p.Arg843Arg | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 20/20 | 2808/3536 | 2529/2868 | 843/955 | chr11 | 61259014 | |||
| chr11:61264520 | G | A | 1 | a0001c0012 | 2 | HG02647.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.2197C>T | p.Leu733Leu | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/20 | 2476/3536 | 2197/2868 | 733/955 | chr11 | 61264520 | |||
| chr11:61265147 | G | A | 1 | a0001c0013 | 2 | HG02615.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.2031C>T | p.Asp677Asp | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 17/20 | 2310/3536 | 2031/2868 | 677/955 | chr11 | 61265147 | |||
| chr11:61265171 | G | C | 1 | a0001c0014 | 2 | HG02056.hp2 NA18945.hp2 |
synonymous_variant | LOW | c.2007C>G | p.Thr669Thr | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 17/20 | 2286/3536 | 2007/2868 | 669/955 | chr11 | 61265171 | |||
| chr11:61274568 | G | A | 1 | a0001c0002 | 16 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(13): Show |
synonymous_variant | LOW | c.1512C>T | p.His504His | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/20 | 1791/3536 | 1512/2868 | 504/955 | chr11 | 61274568 | |||
| chr11:61276615 | C | T | 1 | a0003c0010 | 2 | HG02922.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1473G>A | p.Thr491Thr | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/20 | 1752/3536 | 1473/2868 | 491/955 | chr11 | 61276615 | |||
| chr11:61280850 | G | C | 3 | a0001c0003 a0002c0005 a0011c0018 |
14 | HG01243.hp1 HG01891.hp2 HG02015.hp2 others(11): Show |
synonymous_variant | LOW | c.1173C>G | p.Ala391Ala | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 8/20 | 1452/3536 | 1173/2868 | 391/955 | chr11 | 61280850 | |||
| chr11:61290845 | G | A | 1 | a0001c0024 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.378C>T | p.Pro126Pro | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/20 | 657/3536 | 378/2868 | 126/955 | chr11 | 61290845 | |||
| chr11:61290923 | G | C | 2 | a0001c0002 a0001c0004 |
23 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(20): Show |
synonymous_variant | LOW | c.300C>G | p.Thr100Thr | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/20 | 579/3536 | 300/2868 | 100/955 | chr11 | 61290923 | |||
| chr11:61291316 | G | A | 1 | a0001c0006 | 6 | HG02257.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
synonymous_variant | LOW | c.243C>T | p.Ile81Ile | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 3/20 | 522/3536 | 243/2868 | 81/955 | chr11 | 61291316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61258350 | GTCCCAGT others(8): Show |
G | 2 | a0001c0001t0002 a0012c0016t0002 |
2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*310_*324delTTCCAC others(9): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 20/20 | 310 | chr11 | 61258350 | ||||||
| chr11:61258373 | C | T | 1 | a0001c0001t0003 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*302G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 20/20 | 302 | chr11 | 61258373 | ||||||
| chr11:61258449 | G | C | 1 | a0001c0001t0004 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*226C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 20/20 | 226 | chr11 | 61258449 | ||||||
| chr11:61258510 | G | A | 1 | a0001c0001t0005 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*165C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 20/20 | 165 | chr11 | 61258510 | ||||||
| chr11:61295294 | G | A | 1 | a0001c0001t0006 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-257C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/20 | 257 | chr11 | 61295294 | ||||||
| chr11:61295305 | T | C | 1 | a0001c0002t0007 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-268A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/20 | 268 | chr11 | 61295305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61259387 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2231-75G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61259387 | |||||||
| chr11:61259492 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2231-180C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61259492 | |||||||
| chr11:61259916 | T | C | 61 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0116 others(58): Show |
68 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(65): Show |
intron_variant | MODIFIER | c.2231-604A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61259916 | |||||||
| chr11:61259943 | C | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0119 others(1): Show |
4 | HG01261.hp1 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2231-631G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61259943 | |||||||
| chr11:61259982 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2231-670C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61259982 | |||||||
| chr11:61260030 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2231-718C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61260030 | |||||||
| chr11:61260148 | G | A | 2 | a0001c0004t0001g0029 a0001c0004t0001g0030 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2231-836C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61260148 | |||||||
| chr11:61260161 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2231-849C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61260161 | |||||||
| chr11:61260288 | G | T | 6 | a0001c0003t0001g0145 a0002c0005t0001g0006 a0002c0005t0001g0123 others(3): Show |
8 | HG02015.hp2 HG02165.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.2231-976C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61260288 | |||||||
| chr11:61260366 | T | C | 33 | a0001c0001t0001g0014 a0001c0001t0001g0116 a0001c0001t0001g0122 others(30): Show |
35 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.2231-1054A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61260366 | |||||||
| chr11:61260409 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2231-1097C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61260409 | |||||||
| chr11:61261219 | C | CA | 15 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0016 others(12): Show |
19 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2231-1908dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61261219 | |||||||
| chr11:61261299 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2231-1987A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61261299 | |||||||
| chr11:61261442 | TA | T | 58 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0116 others(55): Show |
65 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(62): Show |
intron_variant | MODIFIER | c.2231-2131delT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61261442 | |||||||
| chr11:61261719 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2231-2407A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61261719 | |||||||
| chr11:61261738 | G | A | 2 | a0007c0011t0001g0155 a0007c0011t0001g0156 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2231-2426C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61261738 | |||||||
| chr11:61261796 | C | A | 7 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0129 others(4): Show |
7 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2231-2484G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61261796 | |||||||
| chr11:61261804 | C | CA | 21 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0036 others(18): Show |
26 | HG00741.hp1 HG01109.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.2231-2493dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61261804 | |||||||
| chr11:61262015 | G | A | 1 | a0001c0002t0001g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2230+2472C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262015 | |||||||
| chr11:61262145 | G | C | 3 | a0001c0001t0001g0121 a0001c0013t0001g0103 a0001c0013t0001g0132 |
3 | HG02615.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2230+2342C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262145 | |||||||
| chr11:61262180 | C | T | 25 | a0001c0001t0001g0106 a0001c0002t0001g0003 a0001c0002t0001g0007 others(22): Show |
30 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2230+2307G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262180 | |||||||
| chr11:61262273 | T | C | 73 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0112 others(70): Show |
80 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(77): Show |
intron_variant | MODIFIER | c.2230+2214A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262273 | |||||||
| chr11:61262431 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2230+2056G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262431 | |||||||
| chr11:61262549 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2230+1938A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262549 | |||||||
| chr11:61262572 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2230+1915A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262572 | |||||||
| chr11:61262692 | G | T | 1 | a0007c0011t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2230+1795C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262692 | |||||||
| chr11:61262698 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2230+1789C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262698 | |||||||
| chr11:61262789 | CCT | C | 6 | a0001c0001t0001g0106 a0001c0006t0001g0011 a0001c0006t0001g0125 others(3): Show |
7 | HG02257.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2230+1696_2230+169 others(6): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262789 | |||||||
| chr11:61262950 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0133 others(3): Show |
6 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2230+1537G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61262950 | |||||||
| chr11:61263143 | C | T | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2230+1344G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263143 | |||||||
| chr11:61263200 | A | G | 33 | a0001c0001t0001g0106 a0001c0001t0001g0112 a0001c0001t0001g0114 others(30): Show |
38 | HG01109.hp2 HG01261.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.2230+1287T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263200 | |||||||
| chr11:61263216 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2230+1271T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263216 | |||||||
| chr11:61263261 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2230+1226G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263261 | |||||||
| chr11:61263303 | C | CA | 19 | a0001c0001t0001g0106 a0001c0001t0001g0112 a0001c0001t0002g0013 others(16): Show |
23 | HG01496.hp1 HG02055.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.2230+1183dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263303 | |||||||
| chr11:61263670 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2230+817T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263670 | |||||||
| chr11:61263760 | G | C | 33 | a0001c0001t0001g0106 a0001c0001t0001g0112 a0001c0001t0001g0114 others(30): Show |
38 | HG01109.hp2 HG01261.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.2230+727C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263760 | |||||||
| chr11:61263781 | G | A | 4 | a0001c0003t0001g0136 a0001c0003t0001g0139 a0001c0003t0001g0140 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2230+706C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263781 | |||||||
| chr11:61263856 | G | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2230+631C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263856 | |||||||
| chr11:61263941 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2230+546C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61263941 | |||||||
| chr11:61264225 | C | CA | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(20): Show |
25 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.2230+261dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61264225 | |||||||
| chr11:61264225 | CA | C | 18 | a0001c0001t0001g0106 a0001c0001t0001g0157 a0001c0001t0002g0013 others(15): Show |
19 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2230+261delT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61264225 | |||||||
| chr11:61264225 | CAA | C | 51 | a0001c0001t0001g0014 a0001c0001t0001g0112 a0001c0001t0001g0114 others(48): Show |
57 | HG01109.hp2 HG01261.hp1 HG01496.hp1 others(54): Show |
intron_variant | MODIFIER | c.2230+260_2230+261d others(4): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61264225 | |||||||
| chr11:61264316 | G | A | 6 | a0001c0021t0001g0113 a0003c0007t0001g0107 a0003c0007t0001g0108 others(3): Show |
6 | HG02615.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2230+171C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61264316 | |||||||
| chr11:61264359 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2230+128C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61264359 | |||||||
| chr11:61264366 | G | A | 6 | a0001c0021t0001g0113 a0003c0007t0001g0107 a0003c0007t0001g0108 others(3): Show |
6 | HG02615.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2230+121C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61264366 | |||||||
| chr11:61264404 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2230+83G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61264404 | |||||||
| chr11:61264454 | C | T | 2 | a0001c0012t0001g0117 a0001c0012t0001g0118 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2230+33G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 19/19 | chr11 | 61264454 | |||||||
| chr11:61264631 | G | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2140-54C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 18/19 | chr11 | 61264631 | |||||||
| chr11:61264749 | C | A | 1 | a0001c0003t0001g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2140-172G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 18/19 | chr11 | 61264749 | |||||||
| chr11:61264786 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2139+170G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 18/19 | chr11 | 61264786 | |||||||
| chr11:61265042 | T | C | 2 | a0001c0001t0002g0013 a0012c0016t0002g0012 |
2 | HG02451.hp1 HG02818.hp1 |
splice_region_variant&intron_variant | LOW | c.2057-4A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 17/19 | chr11 | 61265042 | |||||||
| chr11:61265085 | C | T | 2 | a0007c0011t0001g0155 a0007c0011t0001g0156 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2056+37G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 17/19 | chr11 | 61265085 | |||||||
| chr11:61265098 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2056+24G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 17/19 | chr11 | 61265098 | |||||||
| chr11:61265340 | G | C | 2 | a0001c0012t0001g0117 a0001c0012t0001g0118 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1966-128C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61265340 | |||||||
| chr11:61265360 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1966-148C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61265360 | |||||||
| chr11:61265390 | C | G | 1 | a0007c0011t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1966-178G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61265390 | |||||||
| chr11:61265593 | G | C | 1 | a0007c0011t0001g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1966-381C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61265593 | |||||||
| chr11:61265605 | G | A | 1 | a0001c0001t0006g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1966-393C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61265605 | |||||||
| chr11:61265688 | G | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1966-476C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61265688 | |||||||
| chr11:61265721 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0086 others(6): Show |
14 | HG01109.hp1 HG01168.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1966-509G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61265721 | |||||||
| chr11:61265755 | G | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0086 others(6): Show |
14 | HG01109.hp1 HG01168.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1966-543C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61265755 | |||||||
| chr11:61266023 | C | T | 19 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0147 others(16): Show |
21 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1966-811G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266023 | |||||||
| chr11:61266048 | A | T | 1 | a0001c0002t0001g0007 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1966-836T>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266048 | |||||||
| chr11:61266053 | A | T | 73 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0112 others(70): Show |
80 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(77): Show |
intron_variant | MODIFIER | c.1966-841T>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266053 | |||||||
| chr11:61266054 | A | T | 1 | a0001c0001t0001g0040 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1966-842T>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266054 | |||||||
| chr11:61266462 | C | G | 2 | a0001c0013t0001g0103 a0001c0013t0001g0132 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1965+1000G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266462 | |||||||
| chr11:61266556 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1965+906T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266556 | |||||||
| chr11:61266616 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1965+846A>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266616 | |||||||
| chr11:61266688 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1965+774A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266688 | |||||||
| chr11:61266806 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1965+656G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266806 | |||||||
| chr11:61266829 | C | G | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1965+633G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266829 | |||||||
| chr11:61266863 | A | G | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1965+599T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266863 | |||||||
| chr11:61266921 | G | A | 1 | a0001c0001t0004g0120 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1965+541C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61266921 | |||||||
| chr11:61267020 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0084 others(3): Show |
8 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.1965+442C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61267020 | |||||||
| chr11:61267078 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1965+384G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61267078 | |||||||
| chr11:61267156 | G | C | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1965+306C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61267156 | |||||||
| chr11:61267183 | G | A | 2 | a0001c0013t0001g0103 a0001c0013t0001g0132 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1965+279C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61267183 | |||||||
| chr11:61267184 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1965+278C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61267184 | |||||||
| chr11:61267418 | G | T | 1 | a0008c0023t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1965+44C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 16/19 | chr11 | 61267418 | |||||||
| chr11:61268231 | T | G | 1 | a0001c0001t0001g0081 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1883-687A>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 15/19 | chr11 | 61268231 | |||||||
| chr11:61268485 | T | C | 61 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0116 others(58): Show |
68 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(65): Show |
intron_variant | MODIFIER | c.1882+437A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 15/19 | chr11 | 61268485 | |||||||
| chr11:61268510 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1882+412G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 15/19 | chr11 | 61268510 | |||||||
| chr11:61268662 | G | A | 1 | a0004c0008t0001g0005 | 3 | HG01069.hp1 HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1882+260C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 15/19 | chr11 | 61268662 | |||||||
| chr11:61268842 | A | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0068 |
3 | HG00423.hp2 HG00597.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1882+80T>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 15/19 | chr11 | 61268842 | |||||||
| chr11:61269144 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1786-126G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61269144 | |||||||
| chr11:61269445 | C | CT | 16 | a0001c0001t0001g0014 a0001c0001t0001g0116 a0001c0001t0001g0122 others(13): Show |
17 | HG01109.hp1 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1786-428dupA | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61269445 | |||||||
| chr11:61269595 | G | A | 2 | a0007c0011t0001g0155 a0007c0011t0001g0156 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1786-577C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61269595 | |||||||
| chr11:61269806 | C | T | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1786-788G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61269806 | |||||||
| chr11:61269917 | AT | A | 10 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0121 others(7): Show |
10 | HG02572.hp1 HG02602.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1786-900delA | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61269917 | |||||||
| chr11:61269917 | ATT | A | 59 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0116 others(56): Show |
66 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(63): Show |
intron_variant | MODIFIER | c.1786-901_1786-900d others(4): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61269917 | |||||||
| chr11:61269928 | T | G | 2 | a0007c0011t0001g0155 a0007c0011t0001g0156 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1786-910A>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61269928 | |||||||
| chr11:61269969 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1786-951C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61269969 | |||||||
| chr11:61270066 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0002g0013 a0012c0016t0002g0012 |
3 | HG01515.hp1 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1786-1048G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270066 | |||||||
| chr11:61270241 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1786-1223G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270241 | |||||||
| chr11:61270381 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1785+1294G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270381 | |||||||
| chr11:61270487 | C | T | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1785+1188G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270487 | |||||||
| chr11:61270790 | G | T | 1 | a0008c0023t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1785+885C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270790 | |||||||
| chr11:61270825 | C | CT | 30 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0106 others(27): Show |
32 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1785+849dupA | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270825 | |||||||
| chr11:61270825 | C | CTT | 8 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0129 others(5): Show |
8 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1785+848_1785+849d others(4): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270825 | |||||||
| chr11:61270825 | CT | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0067 a0001c0001t0001g0076 others(4): Show |
7 | HG01515.hp2 HG02132.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+849delA | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270825 | |||||||
| chr11:61270846 | G | T | 7 | a0001c0001t0001g0106 a0001c0021t0001g0113 a0003c0007t0001g0107 others(4): Show |
7 | HG02615.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1785+829C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270846 | |||||||
| chr11:61270983 | A | G | 2 | a0001c0013t0001g0103 a0001c0013t0001g0132 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1785+692T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61270983 | |||||||
| chr11:61271238 | C | T | 1 | a0001c0002t0001g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1785+437G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271238 | |||||||
| chr11:61271239 | G | A | 2 | a0001c0001t0001g0048 a0001c0013t0001g0103 |
2 | HG02080.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1785+436C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271239 | |||||||
| chr11:61271302 | C | T | 1 | a0001c0012t0001g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1785+373G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271302 | |||||||
| chr11:61271457 | T | A | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1785+218A>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271457 | |||||||
| chr11:61271459 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1785+216G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271459 | |||||||
| chr11:61271502 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1785+173C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271502 | |||||||
| chr11:61271563 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1785+112C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271563 | |||||||
| chr11:61271587 | G | A | 61 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0116 others(58): Show |
68 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(65): Show |
intron_variant | MODIFIER | c.1785+88C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271587 | |||||||
| chr11:61271604 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0006g0158 |
2 | HG02135.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1785+71C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271604 | |||||||
| chr11:61271631 | G | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0066 |
2 | HG02080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1785+44C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271631 | |||||||
| chr11:61271635 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1785+40C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 14/19 | chr11 | 61271635 | |||||||
| chr11:61271789 | C | T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0116 a0001c0001t0001g0122 others(30): Show |
35 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.1700-29G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61271789 | |||||||
| chr11:61271850 | C | G | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1700-90G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61271850 | |||||||
| chr11:61271857 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1700-97G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61271857 | |||||||
| chr11:61271927 | TCA | T | 2 | a0001c0001t0001g0122 a0001c0024t0001g0095 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1700-169_1700-168d others(4): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61271927 | |||||||
| chr11:61272158 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1700-398T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61272158 | |||||||
| chr11:61272174 | AAC | A | 14 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0016 others(11): Show |
18 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1700-416_1700-415d others(4): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61272174 | |||||||
| chr11:61272201 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1700-441T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61272201 | |||||||
| chr11:61272311 | C | T | 4 | a0001c0006t0001g0011 a0001c0006t0001g0125 a0001c0006t0001g0126 others(1): Show |
5 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1700-551G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61272311 | |||||||
| chr11:61272391 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0116 a0001c0001t0001g0122 others(5): Show |
8 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1700-631T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61272391 | |||||||
| chr11:61272605 | T | C | 69 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0112 others(66): Show |
76 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(73): Show |
intron_variant | MODIFIER | c.1699+594A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61272605 | |||||||
| chr11:61272718 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1699+481T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61272718 | |||||||
| chr11:61272721 | C | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0114 a0001c0001t0001g0121 others(2): Show |
5 | HG02647.hp2 HG02896.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1699+478G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61272721 | |||||||
| chr11:61272779 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0091 |
2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1699+420T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61272779 | |||||||
| chr11:61273051 | A | AAAC | 73 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0112 others(70): Show |
80 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(77): Show |
intron_variant | MODIFIER | c.1699+147_1699+148i others(5): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61273051 | |||||||
| chr11:61273176 | G | A | 12 | a0001c0003t0001g0136 a0001c0003t0001g0137 a0001c0003t0001g0138 others(9): Show |
14 | HG01243.hp1 HG01891.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1699+23C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 13/19 | chr11 | 61273176 | |||||||
| chr11:61273342 | G | A | 2 | a0001c0013t0001g0103 a0001c0013t0001g0132 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1582-26C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61273342 | |||||||
| chr11:61273432 | T | A | 1 | a0001c0001t0001g0015 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1582-116A>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61273432 | |||||||
| chr11:61273523 | G | A | 6 | a0001c0021t0001g0113 a0003c0007t0001g0107 a0003c0007t0001g0108 others(3): Show |
6 | HG02615.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1582-207C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61273523 | |||||||
| chr11:61273796 | G | C | 2 | a0001c0003t0001g0137 a0001c0003t0001g0138 |
2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1582-480C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61273796 | |||||||
| chr11:61273850 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1582-534G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61273850 | |||||||
| chr11:61274170 | C | T | 6 | a0001c0021t0001g0113 a0003c0007t0001g0107 a0003c0007t0001g0108 others(3): Show |
6 | HG02615.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1581+329G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61274170 | |||||||
| chr11:61274223 | G | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1581+276C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61274223 | |||||||
| chr11:61274245 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1581+254C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61274245 | |||||||
| chr11:61274287 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1581+212T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61274287 | |||||||
| chr11:61274317 | A | C | 6 | a0001c0021t0001g0113 a0003c0007t0001g0107 a0003c0007t0001g0108 others(3): Show |
6 | HG02615.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1581+182T>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 12/19 | chr11 | 61274317 | |||||||
| chr11:61274669 | C | T | 2 | a0003c0010t0001g0035 a0003c0010t0001g0104 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1496-85G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61274669 | |||||||
| chr11:61274773 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1496-189C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61274773 | |||||||
| chr11:61274997 | G | A | 2 | a0001c0004t0001g0029 a0001c0004t0001g0030 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1496-413C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61274997 | |||||||
| chr11:61275576 | G | A | 2 | a0001c0013t0001g0103 a0001c0013t0001g0132 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1496-992C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61275576 | |||||||
| chr11:61275759 | A | T | 27 | a0001c0001t0001g0014 a0001c0001t0001g0116 a0001c0001t0001g0122 others(24): Show |
29 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1495+834T>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61275759 | |||||||
| chr11:61275852 | C | T | 7 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0129 others(4): Show |
7 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495+741G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61275852 | |||||||
| chr11:61276301 | C | G | 69 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0112 others(66): Show |
76 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(73): Show |
intron_variant | MODIFIER | c.1495+292G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61276301 | |||||||
| chr11:61276320 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1495+273G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61276320 | |||||||
| chr11:61276356 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1495+237T>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61276356 | |||||||
| chr11:61276409 | C | CA | 5 | a0001c0021t0001g0113 a0003c0007t0001g0108 a0003c0007t0001g0109 others(2): Show |
5 | HG02615.hp1 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1495+183dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61276409 | |||||||
| chr11:61276438 | C | G | 19 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0016 others(16): Show |
23 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1495+155G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61276438 | |||||||
| chr11:61276439 | T | C | 33 | a0001c0001t0001g0106 a0001c0001t0001g0112 a0001c0001t0001g0114 others(30): Show |
38 | HG01109.hp2 HG01261.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.1495+154A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 11/19 | chr11 | 61276439 | |||||||
| chr11:61276707 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0001g0073 |
3 | HG02027.hp1 NA19077.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1408-27C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61276707 | |||||||
| chr11:61276729 | G | T | 2 | a0001c0013t0001g0103 a0001c0013t0001g0132 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1408-49C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61276729 | |||||||
| chr11:61276736 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0072 |
3 | HG01168.hp1 HG01169.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1408-56G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61276736 | |||||||
| chr11:61276890 | G | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0084 others(3): Show |
8 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408-210C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61276890 | |||||||
| chr11:61276998 | C | G | 69 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0112 others(66): Show |
76 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(73): Show |
intron_variant | MODIFIER | c.1408-318G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61276998 | |||||||
| chr11:61277035 | G | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0134 |
2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1408-355C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277035 | |||||||
| chr11:61277142 | AAAC | A | 2 | a0001c0001t0001g0067 a0013c0019t0001g0034 |
2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1408-465_1408-463d others(5): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277142 | |||||||
| chr11:61277168 | AGGAG | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0001g0073 others(1): Show |
4 | HG02027.hp1 NA18945.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408-492_1408-489d others(6): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277168 | |||||||
| chr11:61277184 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0133 others(3): Show |
6 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408-504C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277184 | |||||||
| chr11:61277291 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1408-611A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277291 | |||||||
| chr11:61277310 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1408-630G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277310 | |||||||
| chr11:61277323 | T | C | 2 | a0001c0021t0001g0113 a0014c0017t0001g0110 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1408-643A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277323 | |||||||
| chr11:61277342 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1408-662G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277342 | |||||||
| chr11:61277364 | T | G | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1408-684A>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277364 | |||||||
| chr11:61277401 | G | A | 24 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0016 others(21): Show |
29 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1408-721C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277401 | |||||||
| chr11:61277445 | C | CA | 22 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0078 others(19): Show |
22 | HG00423.hp1 HG01261.hp1 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.1408-766dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277445 | |||||||
| chr11:61277568 | A | G | 2 | a0001c0001t0002g0013 a0012c0016t0002g0012 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1407+826T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277568 | |||||||
| chr11:61277955 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1407+439G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61277955 | |||||||
| chr11:61278018 | T | G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG01261.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1407+376A>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61278018 | |||||||
| chr11:61278277 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02027.hp2 HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1407+117C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61278277 | |||||||
| chr11:61278317 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1407+77C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61278317 | |||||||
| chr11:61278349 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1407+45C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61278349 | |||||||
| chr11:61278370 | C | T | 2 | a0001c0013t0001g0103 a0001c0013t0001g0132 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1407+24G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 10/19 | chr11 | 61278370 | |||||||
| chr11:61278526 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02015.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1325-50C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61278526 | |||||||
| chr11:61278805 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1325-329G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61278805 | |||||||
| chr11:61278824 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1325-348T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61278824 | |||||||
| chr11:61278895 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1325-419A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61278895 | |||||||
| chr11:61278975 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1325-499C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61278975 | |||||||
| chr11:61279138 | A | C | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(76): Show |
88 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.1325-662T>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61279138 | |||||||
| chr11:61279235 | C | A | 1 | a0007c0011t0001g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1325-759G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61279235 | |||||||
| chr11:61279280 | G | T | 2 | a0001c0013t0001g0103 a0001c0013t0001g0132 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1325-804C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61279280 | |||||||
| chr11:61279404 | C | T | 73 | a0001c0001t0001g0014 a0001c0001t0001g0106 a0001c0001t0001g0112 others(70): Show |
80 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(77): Show |
intron_variant | MODIFIER | c.1325-928G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61279404 | |||||||
| chr11:61279590 | A | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0116 a0001c0001t0001g0122 others(5): Show |
8 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1324+1034T>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61279590 | |||||||
| chr11:61279747 | C | A | 1 | a0001c0001t0001g0031 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1324+877G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61279747 | |||||||
| chr11:61279797 | C | T | 1 | a0001c0004t0001g0027 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1324+827G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61279797 | |||||||
| chr11:61279887 | G | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1324+737C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61279887 | |||||||
| chr11:61280019 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1324+605C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61280019 | |||||||
| chr11:61280394 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1324+230T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61280394 | |||||||
| chr11:61280486 | C | T | 2 | a0001c0001t0002g0013 a0012c0016t0002g0012 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1324+138G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61280486 | |||||||
| chr11:61280540 | T | C | 18 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0016 others(15): Show |
22 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1324+84A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 9/19 | chr11 | 61280540 | |||||||
| chr11:61280724 | G | C | 12 | a0001c0003t0001g0136 a0001c0003t0001g0137 a0001c0003t0001g0138 others(9): Show |
14 | HG01243.hp1 HG01891.hp2 HG02015.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1231-7C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 8/19 | chr11 | 61280724 | |||||||
| chr11:61281501 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.788-266C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 7/19 | chr11 | 61281501 | |||||||
| chr11:61281711 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.787+75G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 7/19 | chr11 | 61281711 | |||||||
| chr11:61282033 | G | C | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.659-119C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 6/19 | chr11 | 61282033 | |||||||
| chr11:61282216 | A | G | 1 | a0001c0002t0001g0022 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.659-302T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 6/19 | chr11 | 61282216 | |||||||
| chr11:61282365 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.658+424C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 6/19 | chr11 | 61282365 | |||||||
| chr11:61282389 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.658+400T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 6/19 | chr11 | 61282389 | |||||||
| chr11:61282659 | G | A | 32 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(29): Show |
37 | HG01109.hp2 HG01261.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.658+130C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 6/19 | chr11 | 61282659 | |||||||
| chr11:61282977 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0097 |
2 | HG01081.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.542-72G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61282977 | |||||||
| chr11:61283105 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.542-200G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61283105 | |||||||
| chr11:61283115 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.542-210G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61283115 | |||||||
| chr11:61283186 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.542-281T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61283186 | |||||||
| chr11:61283229 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.542-324G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61283229 | |||||||
| chr11:61283679 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0085 |
3 | HG00099.hp1 HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.542-774C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61283679 | |||||||
| chr11:61283759 | C | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.542-854G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61283759 | |||||||
| chr11:61284133 | C | G | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(76): Show |
88 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.542-1228G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61284133 | |||||||
| chr11:61284208 | A | C | 1 | a0001c0001t0006g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.542-1303T>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61284208 | |||||||
| chr11:61284521 | G | A | 1 | a0001c0024t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.542-1616C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61284521 | |||||||
| chr11:61284578 | G | A | 8 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG01261.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.542-1673C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61284578 | |||||||
| chr11:61284613 | T | C | 6 | a0001c0001t0001g0106 a0001c0006t0001g0011 a0001c0006t0001g0125 others(3): Show |
7 | HG02257.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+1701A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61284613 | |||||||
| chr11:61284719 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.541+1595C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61284719 | |||||||
| chr11:61285331 | C | T | 2 | a0007c0011t0001g0155 a0007c0011t0001g0156 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.541+983G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61285331 | |||||||
| chr11:61285628 | G | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0094 |
2 | HG01346.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.541+686C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61285628 | |||||||
| chr11:61285793 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG01109.hp1 HG02027.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+521C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61285793 | |||||||
| chr11:61285881 | G | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.541+433C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61285881 | |||||||
| chr11:61286001 | G | A | 1 | a0001c0024t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.541+313C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61286001 | |||||||
| chr11:61286017 | G | C | 3 | a0001c0006t0001g0011 a0001c0006t0001g0125 a0001c0006t0001g0126 |
4 | HG02572.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+297C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61286017 | |||||||
| chr11:61286118 | C | T | 7 | a0001c0001t0001g0106 a0001c0021t0001g0113 a0003c0007t0001g0107 others(4): Show |
7 | HG02615.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.541+196G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61286118 | |||||||
| chr11:61286224 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.541+90C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61286224 | |||||||
| chr11:61286280 | C | T | 2 | a0001c0004t0001g0029 a0001c0004t0001g0030 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.541+34G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 5/19 | chr11 | 61286280 | |||||||
| chr11:61286449 | C | T | 25 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0129 others(22): Show |
27 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.425-19G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61286449 | |||||||
| chr11:61286604 | C | G | 9 | a0001c0001t0001g0106 a0001c0021t0001g0113 a0003c0007t0001g0107 others(6): Show |
9 | HG02615.hp1 HG02630.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-174G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61286604 | |||||||
| chr11:61286620 | G | A | 25 | a0001c0001t0001g0116 a0001c0002t0001g0003 a0001c0002t0001g0007 others(22): Show |
30 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-190C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61286620 | |||||||
| chr11:61286818 | C | T | 1 | a0008c0023t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.425-388G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61286818 | |||||||
| chr11:61286819 | C | T | 2 | a0001c0001t0002g0013 a0012c0016t0002g0012 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.425-389G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61286819 | |||||||
| chr11:61286925 | G | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.425-495C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61286925 | |||||||
| chr11:61287061 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.425-631G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61287061 | |||||||
| chr11:61287132 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.425-702G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61287132 | |||||||
| chr11:61287245 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.425-815C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61287245 | |||||||
| chr11:61287396 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.425-966C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61287396 | |||||||
| chr11:61287420 | C | A | 72 | a0001c0001t0001g0014 a0001c0001t0001g0088 a0001c0001t0001g0106 others(69): Show |
79 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(76): Show |
intron_variant | MODIFIER | c.425-990G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61287420 | |||||||
| chr11:61287476 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.425-1046A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61287476 | |||||||
| chr11:61287542 | GACTA | G | 69 | a0001c0001t0001g0014 a0001c0001t0001g0088 a0001c0001t0001g0106 others(66): Show |
76 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(73): Show |
intron_variant | MODIFIER | c.425-1116_425-1113d others(6): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61287542 | |||||||
| chr11:61287641 | T | C | 1 | a0001c0004t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.425-1211A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61287641 | |||||||
| chr11:61287816 | G | A | 4 | a0001c0004t0001g0025 a0001c0004t0001g0026 a0001c0004t0001g0027 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-1386C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61287816 | |||||||
| chr11:61288112 | G | A | 60 | a0001c0001t0001g0014 a0001c0001t0001g0088 a0001c0001t0001g0106 others(57): Show |
67 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(64): Show |
intron_variant | MODIFIER | c.425-1682C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288112 | |||||||
| chr11:61288116 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.425-1686G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288116 | |||||||
| chr11:61288155 | C | CA | 30 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0077 others(27): Show |
32 | HG01515.hp1 HG01515.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.425-1726dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288155 | |||||||
| chr11:61288155 | C | CAA | 25 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(22): Show |
26 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.425-1727_425-1726d others(4): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288155 | |||||||
| chr11:61288155 | C | CAAA | 17 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0119 others(14): Show |
21 | HG01243.hp1 HG01261.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.425-1728_425-1726d others(5): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288155 | |||||||
| chr11:61288155 | CA | C | 5 | a0001c0001t0001g0031 a0001c0001t0005g0102 a0007c0011t0001g0155 others(2): Show |
5 | HG00558.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-1726delT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288155 | |||||||
| chr11:61288155 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.425-1735_425-1726d others(12): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288155 | |||||||
| chr11:61288515 | G | A | 2 | a0001c0021t0001g0113 a0014c0017t0001g0110 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.425-2085C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288515 | |||||||
| chr11:61288818 | C | G | 2 | a0007c0011t0001g0155 a0007c0011t0001g0156 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+1981G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288818 | |||||||
| chr11:61288839 | G | GT | 40 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(37): Show |
46 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.424+1959dupA | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288839 | |||||||
| chr11:61288839 | GT | G | 6 | a0001c0021t0001g0113 a0003c0007t0001g0107 a0003c0007t0001g0108 others(3): Show |
6 | HG02615.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+1959delA | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288839 | |||||||
| chr11:61288851 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.424+1948A>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288851 | |||||||
| chr11:61288925 | G | A | 2 | a0001c0012t0001g0117 a0001c0012t0001g0118 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.424+1874C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61288925 | |||||||
| chr11:61289488 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.424+1311C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61289488 | |||||||
| chr11:61289525 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.424+1274G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61289525 | |||||||
| chr11:61289747 | A | C | 1 | a0001c0001t0005g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.424+1052T>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61289747 | |||||||
| chr11:61289980 | T | C | 1 | a0001c0002t0001g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.424+819A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61289980 | |||||||
| chr11:61290250 | G | A | 2 | a0001c0001t0002g0013 a0012c0016t0002g0012 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.424+549C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290250 | |||||||
| chr11:61290327 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.424+472G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290327 | |||||||
| chr11:61290474 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.424+325A>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290474 | |||||||
| chr11:61290511 | C | CA | 8 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(5): Show |
8 | HG01106.hp2 HG01243.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+287dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290511 | |||||||
| chr11:61290511 | CA | C | 12 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(9): Show |
12 | HG01884.hp1 HG02647.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.424+287delT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290511 | |||||||
| chr11:61290592 | CT | C | 5 | a0001c0006t0001g0011 a0001c0006t0001g0125 a0001c0006t0001g0126 others(2): Show |
6 | HG02257.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+206delA | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290592 | |||||||
| chr11:61290649 | C | G | 3 | a0001c0006t0001g0011 a0001c0006t0001g0125 a0001c0006t0001g0126 |
4 | HG02572.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+150G>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290649 | |||||||
| chr11:61290736 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.424+63C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290736 | |||||||
| chr11:61290737 | G | T | 1 | a0001c0001t0003g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.424+62C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290737 | |||||||
| chr11:61290754 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.424+45G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290754 | |||||||
| chr11:61290791 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG00323.hp2 | splice_region_variant&intron_variant | LOW | c.424+8G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 4/19 | chr11 | 61290791 | |||||||
| chr11:61290959 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.296-32G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 3/19 | chr11 | 61290959 | |||||||
| chr11:61291044 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.296-117C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 3/19 | chr11 | 61291044 | |||||||
| chr11:61291372 | G | A | 24 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0016 others(21): Show |
29 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.206-19C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 2/19 | chr11 | 61291372 | |||||||
| chr11:61291395 | T | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
104 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(101): Show |
intron_variant | MODIFIER | c.206-42A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 2/19 | chr11 | 61291395 | |||||||
| chr11:61291896 | A | G | 4 | a0001c0004t0001g0025 a0001c0004t0001g0026 a0001c0004t0001g0027 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-320T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61291896 | |||||||
| chr11:61292160 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.111-584A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292160 | |||||||
| chr11:61292238 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.111-662T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292238 | |||||||
| chr11:61292238 | AAGAG | A | 14 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0016 others(11): Show |
18 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-666_111-663del others(4): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292238 | |||||||
| chr11:61292442 | T | C | 1 | a0001c0024t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.111-866A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292442 | |||||||
| chr11:61292455 | A | G | 1 | a0001c0024t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.111-879T>C | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292455 | |||||||
| chr11:61292465 | G | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.111-889C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292465 | |||||||
| chr11:61292581 | G | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0038 others(3): Show |
6 | HG01106.hp1 HG02027.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-1005C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292581 | |||||||
| chr11:61292745 | G | A | 6 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0021 others(3): Show |
10 | HG01496.hp1 HG02055.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.111-1169C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292745 | |||||||
| chr11:61292889 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.111-1313G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292889 | |||||||
| chr11:61292974 | G | A | 1 | a0003c0007t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.111-1398C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61292974 | |||||||
| chr11:61293182 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0094 |
2 | HG01346.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.111-1606C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293182 | |||||||
| chr11:61293241 | C | CA | 19 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(16): Show |
19 | HG01261.hp2 HG01891.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.111-1666dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293241 | C | CAA | 8 | a0001c0001t0001g0112 a0001c0001t0001g0157 a0001c0006t0001g0011 others(5): Show |
9 | HG02257.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-1667_111-1666d others(4): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293241 | C | CAAA | 7 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(4): Show |
7 | HG01261.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.111-1668_111-1666d others(5): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293241 | C | CAAAA | 14 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0133 others(11): Show |
16 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.111-1669_111-1666d others(6): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293241 | C | CAAAAA | 9 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0147 others(6): Show |
9 | HG01884.hp1 HG02015.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-1670_111-1666d others(7): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293241 | C | CAAAAAA | 5 | a0001c0001t0001g0149 a0001c0004t0001g0025 a0001c0004t0001g0026 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-1671_111-1666d others(8): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293241 | C | CAAAAAAA others(1): Show |
12 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0017 others(9): Show |
16 | HG01496.hp1 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.111-1673_111-1666d others(10): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293241 | C | CAAAAAAA others(3): Show |
2 | a0001c0002t0007g0159 a0001c0004t0001g0124 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.111-1675_111-1666d others(12): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293241 | CA | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0036 others(2): Show |
5 | HG01081.hp1 HG02735.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-1666delT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293241 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.110+1674_111-1666d others(15): Show |
VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293241 | |||||||
| chr11:61293366 | G | A | 5 | a0001c0006t0001g0011 a0001c0006t0001g0125 a0001c0006t0001g0126 others(2): Show |
6 | HG02257.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+1562C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293366 | |||||||
| chr11:61293416 | C | CA | 24 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0133 others(21): Show |
26 | HG00558.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.110+1511dupT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293416 | |||||||
| chr11:61293416 | CA | C | 16 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
20 | HG01496.hp1 HG01516.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.110+1511delT | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293416 | |||||||
| chr11:61293440 | G | T | 18 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0016 others(15): Show |
22 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.110+1488C>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293440 | |||||||
| chr11:61293657 | C | A | 2 | a0006c0009t0001g0150 a0006c0009t0001g0151 |
2 | HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110+1271G>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293657 | |||||||
| chr11:61293889 | G | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02027.hp2 HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.110+1039C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293889 | |||||||
| chr11:61293957 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.110+971G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61293957 | |||||||
| chr11:61294016 | G | C | 2 | a0007c0011t0001g0155 a0007c0011t0001g0156 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.110+912C>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61294016 | |||||||
| chr11:61294305 | T | C | 2 | a0001c0001t0002g0013 a0012c0016t0002g0012 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.110+623A>G | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61294305 | |||||||
| chr11:61294365 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+563G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61294365 | |||||||
| chr11:61294845 | C | T | 2 | a0001c0001t0002g0013 a0012c0016t0002g0012 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.110+83G>A | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61294845 | |||||||
| chr11:61294922 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | splice_region_variant&intron_variant | LOW | c.110+6C>T | VWCE | ENSG00000167992.14 | transcript | ENST00000335613.10 | protein_coding | 1/19 | chr11 | 61294922 |