Item | Value |
---|---|
geneid | 3732 |
ensemblid | ENSG00000085117.12 |
hgncid | 6210 |
symbol | CD82 |
name | CD82 molecule |
refseq_nuc | NM_002231.4 |
refseq_prot | NP_002222.1 |
ensembl_nuc | ENST00000227155.9 |
ensembl_prot | ENSP00000227155.4 |
mane_status | MANE Select |
chr | chr11 |
start | 44565663 |
end | 44620358 |
strand | + |
ver | v1.2 |
region | chr11:44565663-44620358 |
region5000 | chr11:44560663-44625358 |
regionname0 | CD82_chr11_44565663_44620358 |
regionname5000 | CD82_chr11_44560663_44625358 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 267 | 190 | 60 | 28 | 80 | 9 | 11 | 56 | CD82_chr11_44560663_44625358 | CD82 | MGSAC others(262): Show |
chr11 | 44560663 | 44625358 |
a0002 | 0/0 | 267 | 181 | 32 | 52 | 59 | 7 | 31 | 43 | CD82_chr11_44560663_44625358 | CD82 | MGSAC others(262): Show |
chr11 | 44560663 | 44625358 |
a0003 | 0/0 | 267 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | MGSAC others(262): Show |
chr11 | 44560663 | 44625358 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 801 | 105 | 41 | 24 | 24 | 6 | 9 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0005 | 0/0 | 801 | 19 | 1 | 0 | 18 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0006 | 0/1 | 801 | 15 | 0 | 1 | 10 | 2 | 1 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0009 | 0/0 | 801 | 13 | 4 | 0 | 8 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0010 | 0/0 | 801 | 12 | 4 | 3 | 5 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0011 | 0/0 | 801 | 11 | 0 | 0 | 11 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0012 | 0/0 | 801 | 5 | 5 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0014 | 0/0 | 801 | 4 | 0 | 0 | 3 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0016 | 0/0 | 801 | 3 | 3 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0018 | 0/0 | 801 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0001c0023 | 0/0 | 801 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0002 | 0/0 | 801 | 62 | 1 | 15 | 32 | 1 | 13 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0003 | 0/0 | 801 | 47 | 21 | 17 | 3 | 1 | 5 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0004 | 0/0 | 801 | 28 | 1 | 8 | 7 | 2 | 10 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0007 | 0/0 | 801 | 14 | 3 | 9 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0008 | 0/0 | 801 | 13 | 0 | 0 | 11 | 0 | 2 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0013 | 0/0 | 801 | 4 | 0 | 1 | 0 | 3 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0015 | 0/0 | 801 | 4 | 3 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0017 | 0/0 | 801 | 3 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0019 | 0/0 | 801 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0020 | 0/0 | 801 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0021 | 0/0 | 801 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0024 | 0/0 | 801 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0025 | 0/0 | 801 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0002c0026 | 0/0 | 801 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 | ||
a0003c0022 | 0/0 | 801 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | ATGGG others(796): Show |
chr11 | 44560663 | 44625358 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2211 | 36 | 5 | 9 | 13 | 4 | 5 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0002 | 0/0 | 2210 | 8 | 2 | 0 | 5 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0003 | 0/0 | 2212 | 13 | 3 | 8 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0004 | 0/0 | 2213 | 12 | 12 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0005 | 0/0 | 2212 | 3 | 0 | 1 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0006 | 0/0 | 2212 | 4 | 0 | 3 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0007 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2209): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0008 | 0/0 | 2211 | 4 | 4 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0011 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0012 | 1/0 | 2212 | 3 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0013 | 0/0 | 2211 | 4 | 0 | 1 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0014 | 0/0 | 2212 | 2 | 1 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0015 | 0/0 | 2210 | 3 | 3 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0016 | 0/0 | 2210 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0017 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0018 | 0/0 | 2213 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0025 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0026 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0027 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0046 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0049 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0050 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0001t0051 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0005t0001 | 0/0 | 2211 | 4 | 1 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0005t0002 | 0/0 | 2210 | 8 | 0 | 0 | 8 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0005t0003 | 0/0 | 2212 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0005t0004 | 0/0 | 2213 | 3 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0005t0034 | 0/0 | 2210 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0005t0037 | 0/0 | 2212 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0006t0001 | 0/1 | 2211 | 4 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0006t0002 | 0/0 | 2210 | 5 | 0 | 0 | 5 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0006t0003 | 0/0 | 2212 | 4 | 0 | 1 | 2 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0006t0005 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0006t0024 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0009t0001 | 0/0 | 2211 | 3 | 1 | 0 | 1 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0009t0002 | 0/0 | 2210 | 3 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0009t0003 | 0/0 | 2212 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0009t0004 | 0/0 | 2213 | 2 | 1 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0009t0010 | 0/0 | 2209 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2204): Show |
chr11 | 44560663 | 44625358 |
a0001c0009t0011 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0009t0015 | 0/0 | 2210 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0010t0001 | 0/0 | 2211 | 3 | 0 | 2 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0010t0002 | 0/0 | 2210 | 2 | 0 | 1 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0010t0003 | 0/0 | 2212 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0010t0004 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0010t0007 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2209): Show |
chr11 | 44560663 | 44625358 |
a0001c0010t0008 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0010t0040 | 0/0 | 2212 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0011t0001 | 0/0 | 2211 | 3 | 0 | 0 | 3 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0011t0005 | 0/0 | 2212 | 7 | 0 | 0 | 7 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0011t0033 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0012t0003 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0012t0004 | 0/0 | 2213 | 3 | 3 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0012t0016 | 0/0 | 2210 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0014t0001 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0001c0014t0002 | 0/0 | 2210 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0001c0014t0003 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0016t0004 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0016t0017 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0001c0016t0048 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2209): Show |
chr11 | 44560663 | 44625358 |
a0001c0018t0012 | 0/0 | 2212 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0001c0023t0002 | 0/0 | 2210 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0001 | 0/0 | 2211 | 26 | 0 | 11 | 8 | 1 | 6 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0002 | 0/0 | 2210 | 9 | 0 | 0 | 6 | 0 | 3 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0003 | 0/0 | 2212 | 17 | 0 | 3 | 10 | 0 | 4 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0004 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0006 | 0/0 | 2212 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0007 | 0/0 | 2214 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2209): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0020 | 0/0 | 2212 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0022 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0023 | 0/0 | 2212 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0032 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0002t0036 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0001 | 0/0 | 2211 | 14 | 1 | 7 | 3 | 0 | 3 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0002 | 0/0 | 2210 | 4 | 2 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0003 | 0/0 | 2212 | 5 | 1 | 2 | 0 | 1 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0004 | 0/0 | 2213 | 5 | 5 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0005 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0006 | 0/0 | 2212 | 3 | 0 | 3 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0007 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2209): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0008 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0011 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0014 | 0/0 | 2212 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0028 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0029 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0030 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0038 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0041 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0042 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0043 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0044 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0003t0045 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2209): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0001 | 0/0 | 2211 | 8 | 0 | 3 | 2 | 1 | 2 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0002 | 0/0 | 2210 | 4 | 0 | 2 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0003 | 0/0 | 2212 | 4 | 0 | 1 | 1 | 0 | 2 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0009 | 0/0 | 2211 | 5 | 0 | 1 | 0 | 0 | 4 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0016 | 0/0 | 2210 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0018 | 0/0 | 2213 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0019 | 0/0 | 2211 | 2 | 0 | 1 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0021 | 0/0 | 2212 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0035 | 0/0 | 2210 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0004t0039 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0007t0002 | 0/0 | 2210 | 12 | 1 | 9 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0007t0003 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0007t0004 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0008t0001 | 0/0 | 2211 | 5 | 0 | 0 | 5 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0008t0002 | 0/0 | 2210 | 4 | 0 | 0 | 4 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0008t0004 | 0/0 | 2213 | 2 | 0 | 0 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0008t0010 | 0/0 | 2209 | 2 | 0 | 0 | 1 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2204): Show |
chr11 | 44560663 | 44625358 |
a0002c0013t0001 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0013t0003 | 0/0 | 2212 | 3 | 0 | 1 | 0 | 2 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0015t0003 | 0/0 | 2212 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0015t0007 | 0/0 | 2214 | 2 | 2 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2209): Show |
chr11 | 44560663 | 44625358 |
a0002c0015t0031 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0017t0001 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2206): Show |
chr11 | 44560663 | 44625358 |
a0002c0017t0002 | 0/0 | 2210 | 2 | 0 | 0 | 2 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0019t0011 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0020t0010 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2204): Show |
chr11 | 44560663 | 44625358 |
a0002c0021t0003 | 0/0 | 2212 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2207): Show |
chr11 | 44560663 | 44625358 |
a0002c0024t0047 | 0/0 | 2210 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0002c0025t0004 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
a0002c0026t0002 | 0/0 | 2210 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2205): Show |
chr11 | 44560663 | 44625358 |
a0003c0022t0004 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | GCAGT others(2208): Show |
chr11 | 44560663 | 44625358 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0006g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0011g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0012g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0012g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0013g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0013g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0013g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0013g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0014g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0014g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0015g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0015g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0015g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0016g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0017g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0017g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0018g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0025g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0026g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0027g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0046g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0049g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0050g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0001t0051g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0034g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0005t0037g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0005g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0006t0024g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0009t0015g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0010t0040g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0011t0033g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0012t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0012t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0012t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0012t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0012t0016g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0014t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0014t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0014t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0014t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0016t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0016t0017g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0016t0048g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0018t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0018t0012g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0001c0023t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0020g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0020g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0022g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0023g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0032g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0002t0036g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0006g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0006g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0008g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0011g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0014g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0014g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0028g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0029g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0030g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0038g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0041g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0042g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0043g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0044g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0003t0045g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0009g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0009g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0009g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0009g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0009g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0016g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0018g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0019g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0019g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0021g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0035g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0004t0039g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0007t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0010g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0008t0010g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0013t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0013t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0013t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0015t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0015t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0015t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0015t0031g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0017t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0017t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0017t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0019t0011g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0020t0010g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0021t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0024t0047g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0025t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0002c0026t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
a0003c0022t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0004 | t0018 | g0229 | EUR | GBR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0266 | EUR | GBR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00140 | hp1 | a0002 | c0013 | t0001 | g0114 | EUR | GBR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00140 | hp2 | a0002 | c0003 | t0003 | g0295 | EUR | GBR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00323 | hp1 | a0002 | c0004 | t0001 | g0062 | EUR | FIN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0232 | EUR | FIN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00408 | hp1 | a0001 | c0006 | t0002 | g0007 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00408 | hp2 | a0001 | c0005 | t0002 | g0205 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00438 | hp1 | a0001 | c0010 | t0001 | g0122 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00438 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00544 | hp1 | a0001 | c0009 | t0002 | g0136 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00544 | hp2 | a0001 | c0005 | t0002 | g0049 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00558 | hp1 | a0001 | c0010 | t0003 | g0237 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00597 | hp1 | a0001 | c0005 | t0004 | g0073 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00597 | hp2 | a0002 | c0008 | t0002 | g0297 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00609 | hp2 | a0001 | c0009 | t0004 | g0238 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00621 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00621 | hp2 | a0001 | c0001 | t0013 | g0215 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00639 | hp1 | a0001 | c0010 | t0001 | g0211 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00639 | hp2 | a0001 | c0006 | t0003 | g0343 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00642 | hp2 | a0002 | c0026 | t0002 | g0055 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00673 | hp1 | a0002 | c0008 | t0004 | g0090 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00673 | hp2 | a0001 | c0023 | t0002 | g0181 | EAS | CHS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00735 | hp1 | a0002 | c0004 | t0019 | g0058 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00735 | hp2 | a0002 | c0021 | t0003 | g0006 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00738 | hp1 | a0002 | c0002 | t0003 | g0230 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00738 | hp2 | a0002 | c0007 | t0002 | g0050 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00741 | hp1 | a0002 | c0004 | t0001 | g0060 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG00741 | hp2 | a0002 | c0003 | t0006 | g0139 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01070 | hp1 | a0002 | c0004 | t0001 | g0009 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01070 | hp2 | a0002 | c0007 | t0002 | g0013 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0116 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01071 | hp2 | a0002 | c0007 | t0002 | g0014 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01074 | hp2 | a0002 | c0003 | t0003 | g0319 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01081 | hp1 | a0002 | c0004 | t0002 | g0009 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01081 | hp2 | a0002 | c0002 | t0006 | g0173 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01099 | hp1 | a0002 | c0007 | t0002 | g0041 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01099 | hp2 | a0002 | c0002 | t0003 | g0245 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01106 | hp1 | a0002 | c0007 | t0002 | g0042 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01106 | hp2 | a0001 | c0010 | t0001 | g0210 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01109 | hp1 | a0002 | c0003 | t0002 | g0324 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01109 | hp2 | a0001 | c0001 | t0014 | g0279 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01167 | hp1 | a0002 | c0004 | t0002 | g0227 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01167 | hp2 | a0002 | c0007 | t0002 | g0132 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01168 | hp1 | a0002 | c0003 | t0003 | g0005 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01169 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01169 | hp2 | a0002 | c0007 | t0002 | g0131 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0142 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01192 | hp2 | a0001 | c0010 | t0002 | g0015 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01243 | hp1 | a0002 | c0003 | t0043 | g0275 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01243 | hp2 | a0001 | c0001 | t0016 | g0125 | AMR | PUR | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01255 | hp2 | a0001 | c0001 | t0013 | g0072 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01258 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01261 | hp1 | a0002 | c0007 | t0002 | g0056 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01346 | hp2 | a0002 | c0003 | t0002 | g0305 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01358 | hp2 | a0002 | c0003 | t0001 | g0002 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01496 | hp1 | a0002 | c0003 | t0029 | g0274 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01515 | hp2 | a0002 | c0013 | t0003 | g0004 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01516 | hp2 | a0001 | c0009 | t0001 | g0178 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01517 | hp2 | a0002 | c0013 | t0003 | g0004 | EUR | IBS | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01884 | hp1 | a0001 | c0018 | t0012 | g0268 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01884 | hp2 | a0002 | c0003 | t0014 | g0327 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01891 | hp1 | a0002 | c0007 | t0002 | g0128 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0294 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01943 | hp2 | a0002 | c0003 | t0001 | g0217 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01952 | hp2 | a0002 | c0003 | t0001 | g0044 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01978 | hp1 | a0002 | c0003 | t0006 | g0216 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0302 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01981 | hp1 | a0002 | c0013 | t0003 | g0054 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0098 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0147 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02004 | hp1 | a0002 | c0003 | t0030 | g0304 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02004 | hp2 | a0002 | c0004 | t0001 | g0057 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02015 | hp1 | a0002 | c0002 | t0036 | g0119 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02055 | hp1 | a0002 | c0002 | t0022 | g0272 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02055 | hp2 | a0001 | c0016 | t0004 | g0350 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02056 | hp1 | a0001 | c0006 | t0001 | g0037 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02071 | hp1 | a0002 | c0002 | t0023 | g0108 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02071 | hp2 | a0002 | c0002 | t0003 | g0168 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02129 | hp1 | a0002 | c0002 | t0020 | g0152 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02129 | hp2 | a0001 | c0005 | t0001 | g0203 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02132 | hp1 | a0001 | c0006 | t0003 | g0078 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02132 | hp2 | a0001 | c0010 | t0003 | g0170 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02135 | hp1 | a0001 | c0006 | t0001 | g0120 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02135 | hp2 | a0002 | c0004 | t0035 | g0235 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02145 | hp1 | a0002 | c0003 | t0044 | g0267 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02145 | hp2 | a0002 | c0003 | t0042 | g0310 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02148 | hp1 | a0002 | c0003 | t0006 | g0220 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02257 | hp1 | a0001 | c0001 | t0008 | g0197 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02257 | hp2 | a0001 | c0010 | t0007 | g0097 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02258 | hp1 | a0001 | c0001 | t0051 | g0222 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02258 | hp2 | a0001 | c0016 | t0017 | g0031 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02273 | hp2 | a0002 | c0003 | t0001 | g0190 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02280 | hp1 | a0002 | c0003 | t0011 | g0325 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02280 | hp2 | a0002 | c0003 | t0004 | g0251 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02293 | hp1 | a0001 | c0001 | t0006 | g0214 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02293 | hp2 | a0002 | c0004 | t0009 | g0240 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02300 | hp1 | a0002 | c0003 | t0001 | g0027 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02300 | hp2 | a0002 | c0007 | t0002 | g0115 | AMR | PEL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02451 | hp1 | a0001 | c0012 | t0004 | g0257 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02451 | hp2 | a0001 | c0001 | t0012 | g0084 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02523 | hp1 | a0002 | c0008 | t0010 | g0169 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02523 | hp2 | a0002 | c0002 | t0007 | g0077 | EAS | KHV | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02602 | hp1 | a0002 | c0004 | t0001 | g0010 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0262 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02615 | hp2 | a0002 | c0003 | t0005 | g0161 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02622 | hp1 | a0001 | c0009 | t0015 | g0223 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02622 | hp2 | a0001 | c0001 | t0049 | g0342 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02630 | hp1 | a0002 | c0003 | t0008 | g0349 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02630 | hp2 | a0001 | c0009 | t0004 | g0085 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02683 | hp2 | a0001 | c0001 | t0018 | g0198 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0288 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02698 | hp2 | a0002 | c0004 | t0019 | g0040 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02717 | hp1 | a0002 | c0015 | t0003 | g0338 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02717 | hp2 | a0001 | c0012 | t0016 | g0312 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02735 | hp1 | a0002 | c0003 | t0001 | g0012 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02735 | hp2 | a0002 | c0003 | t0003 | g0163 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0309 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0135 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02809 | hp1 | a0001 | c0010 | t0004 | g0095 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02809 | hp2 | a0002 | c0003 | t0004 | g0270 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02818 | hp1 | a0002 | c0003 | t0011 | g0260 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02818 | hp2 | a0001 | c0010 | t0008 | g0247 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02886 | hp1 | a0001 | c0009 | t0001 | g0087 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0320 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02896 | hp1 | a0002 | c0003 | t0004 | g0254 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02897 | hp1 | a0002 | c0003 | t0003 | g0255 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0265 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02965 | hp1 | a0002 | c0003 | t0004 | g0345 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02965 | hp2 | a0002 | c0003 | t0004 | g0252 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02970 | hp2 | a0001 | c0012 | t0004 | g0256 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02976 | hp1 | a0001 | c0018 | t0012 | g0340 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02976 | hp2 | a0002 | c0025 | t0004 | g0348 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03017 | hp1 | a0001 | c0001 | t0026 | g0117 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03017 | hp2 | a0002 | c0002 | t0003 | g0118 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03041 | hp1 | a0001 | c0005 | t0001 | g0264 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03041 | hp2 | a0002 | c0007 | t0003 | g0330 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03098 | hp2 | a0002 | c0015 | t0007 | g0079 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0259 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03139 | hp2 | a0002 | c0003 | t0041 | g0311 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03195 | hp1 | a0002 | c0003 | t0014 | g0258 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03195 | hp2 | a0001 | c0016 | t0048 | g0032 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0248 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0224 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03453 | hp1 | a0002 | c0024 | t0047 | g0282 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03486 | hp1 | a0002 | c0003 | t0045 | g0066 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03486 | hp2 | a0001 | c0012 | t0004 | g0194 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03492 | hp1 | a0002 | c0004 | t0009 | g0010 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0158 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03516 | hp1 | a0001 | c0012 | t0003 | g0339 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0332 | AFR | ESN | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03579 | hp1 | a0001 | c0010 | t0004 | g0188 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03579 | hp2 | a0001 | c0001 | t0050 | g0276 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03654 | hp1 | a0002 | c0004 | t0021 | g0183 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03669 | hp1 | a0002 | c0004 | t0009 | g0244 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03669 | hp2 | a0002 | c0004 | t0001 | g0306 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0053 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03688 | hp2 | a0002 | c0003 | t0038 | g0278 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0089 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0149 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03710 | hp1 | a0001 | c0001 | t0025 | g0284 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03710 | hp2 | a0002 | c0004 | t0003 | g0233 | SAS | PJL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03831 | hp1 | a0002 | c0008 | t0010 | g0165 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03831 | hp2 | a0001 | c0014 | t0003 | g0134 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03834 | hp1 | a0002 | c0002 | t0003 | g0174 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03927 | hp2 | a0002 | c0007 | t0002 | g0064 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG04115 | hp1 | a0001 | c0006 | t0024 | g0296 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG04115 | hp2 | a0002 | c0004 | t0009 | g0236 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0239 | SAS | BEB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG04204 | hp1 | a0002 | c0008 | t0004 | g0231 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0281 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0067 | SAS | STU | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18522 | hp1 | a0001 | c0001 | t0015 | g0351 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18522 | hp2 | a0002 | c0003 | t0002 | g0323 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18612 | hp1 | a0001 | c0005 | t0002 | g0182 | EAS | CHB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | CHB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | CHB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18747 | hp2 | a0002 | c0003 | t0001 | g0068 | EAS | CHB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18906 | hp1 | a0002 | c0003 | t0028 | g0261 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0271 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18939 | hp1 | a0001 | c0005 | t0002 | g0291 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18939 | hp2 | a0002 | c0002 | t0032 | g0138 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18941 | hp1 | a0001 | c0006 | t0002 | g0121 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18941 | hp2 | a0001 | c0005 | t0002 | g0290 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18942 | hp1 | a0001 | c0005 | t0037 | g0083 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18947 | hp1 | a0003 | c0022 | t0004 | g0206 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18948 | hp1 | a0001 | c0009 | t0010 | g0081 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18948 | hp2 | a0002 | c0003 | t0001 | g0086 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18949 | hp1 | a0001 | c0011 | t0033 | g0293 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18949 | hp2 | a0001 | c0005 | t0003 | g0099 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18950 | hp2 | a0001 | c0011 | t0005 | g0148 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18951 | hp1 | a0002 | c0004 | t0001 | g0160 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18951 | hp2 | a0001 | c0005 | t0004 | g0105 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18954 | hp1 | a0002 | c0015 | t0031 | g0219 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18954 | hp2 | a0002 | c0004 | t0002 | g0225 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18957 | hp1 | a0001 | c0010 | t0002 | g0023 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18957 | hp2 | a0002 | c0008 | t0002 | g0111 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18959 | hp1 | a0001 | c0006 | t0002 | g0162 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18959 | hp2 | a0001 | c0009 | t0010 | g0082 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18963 | hp1 | a0002 | c0004 | t0002 | g0226 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18963 | hp2 | a0001 | c0011 | t0005 | g0299 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18965 | hp1 | a0002 | c0002 | t0003 | g0103 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18965 | hp2 | a0001 | c0011 | t0001 | g0335 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18967 | hp1 | a0002 | c0008 | t0001 | g0130 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18973 | hp1 | a0001 | c0011 | t0005 | g0300 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18973 | hp2 | a0001 | c0011 | t0001 | g0333 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18979 | hp1 | a0002 | c0008 | t0001 | g0207 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18979 | hp2 | a0002 | c0004 | t0003 | g0202 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18980 | hp1 | a0002 | c0004 | t0001 | g0074 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18980 | hp2 | a0002 | c0002 | t0007 | g0029 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18984 | hp1 | a0002 | c0007 | t0002 | g0234 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18984 | hp2 | a0002 | c0002 | t0003 | g0036 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18985 | hp1 | a0001 | c0005 | t0001 | g0088 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18988 | hp1 | a0001 | c0011 | t0005 | g0301 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18994 | hp1 | a0002 | c0002 | t0004 | g0127 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18994 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18995 | hp2 | a0001 | c0005 | t0004 | g0075 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18998 | hp1 | a0001 | c0005 | t0003 | g0209 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18998 | hp2 | a0001 | c0001 | t0013 | g0221 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18999 | hp1 | a0001 | c0009 | t0002 | g0186 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA18999 | hp2 | a0001 | c0005 | t0034 | g0187 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19000 | hp1 | a0001 | c0011 | t0005 | g0317 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19000 | hp2 | a0002 | c0004 | t0039 | g0180 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19003 | hp1 | a0002 | c0002 | t0020 | g0007 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19003 | hp2 | a0002 | c0008 | t0001 | g0285 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19004 | hp1 | a0002 | c0017 | t0002 | g0141 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19004 | hp2 | a0001 | c0009 | t0001 | g0033 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19005 | hp1 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19005 | hp2 | a0001 | c0001 | t0013 | g0025 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19007 | hp1 | a0001 | c0005 | t0002 | g0189 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19009 | hp1 | a0002 | c0020 | t0010 | g0167 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19009 | hp2 | a0001 | c0009 | t0003 | g0185 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19011 | hp1 | a0001 | c0005 | t0002 | g0208 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19012 | hp1 | a0001 | c0006 | t0002 | g0151 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19012 | hp2 | a0001 | c0014 | t0002 | g0199 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19030 | hp1 | a0002 | c0007 | t0004 | g0346 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19030 | hp2 | a0001 | c0001 | t0017 | g0091 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19043 | hp1 | a0002 | c0003 | t0007 | g0022 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19043 | hp2 | a0001 | c0001 | t0014 | g0212 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19054 | hp1 | a0002 | c0017 | t0002 | g0334 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19054 | hp2 | a0001 | c0011 | t0005 | g0313 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19057 | hp1 | a0002 | c0008 | t0001 | g0129 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19057 | hp2 | a0001 | c0011 | t0005 | g0337 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19067 | hp2 | a0002 | c0017 | t0001 | g0191 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19070 | hp1 | a0001 | c0011 | t0001 | g0336 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19070 | hp2 | a0001 | c0014 | t0002 | g0026 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19074 | hp1 | a0001 | c0009 | t0002 | g0184 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19074 | hp2 | a0002 | c0002 | t0003 | g0102 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19076 | hp1 | a0001 | c0010 | t0040 | g0030 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19076 | hp2 | a0002 | c0002 | t0003 | g0166 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19081 | hp1 | a0001 | c0006 | t0001 | g0164 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19082 | hp1 | a0001 | c0006 | t0002 | g0155 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19085 | hp1 | a0002 | c0008 | t0002 | g0154 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19086 | hp1 | a0002 | c0008 | t0001 | g0024 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19086 | hp2 | a0001 | c0006 | t0003 | g0201 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19087 | hp1 | a0002 | c0008 | t0002 | g0069 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19087 | hp2 | a0001 | c0005 | t0002 | g0080 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19088 | hp2 | a0001 | c0005 | t0001 | g0204 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19090 | hp1 | a0001 | c0014 | t0001 | g0195 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19090 | hp2 | a0002 | c0002 | t0003 | g0101 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19091 | hp2 | a0002 | c0002 | t0003 | g0347 | EAS | JPT | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19240 | hp1 | a0001 | c0001 | t0027 | g0321 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA19240 | hp2 | a0002 | c0003 | t0002 | g0039 | AFR | YRI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA20752 | hp1 | a0001 | c0006 | t0003 | g0192 | EUR | TSI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0016 | EUR | TSI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA20805 | hp2 | a0001 | c0006 | t0005 | g0273 | EUR | TSI | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA20905 | hp1 | a0002 | c0004 | t0003 | g0218 | SAS | GIH | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA20905 | hp2 | a0002 | c0004 | t0009 | g0063 | SAS | GIH | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0315 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG01123 | hp2 | a0002 | c0004 | t0003 | g0070 | AMR | CLM | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02109 | hp1 | a0002 | c0003 | t0001 | g0093 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02486 | hp1 | a0001 | c0009 | t0011 | g0263 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02559 | hp1 | a0001 | c0001 | t0017 | g0283 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG02559 | hp2 | a0002 | c0019 | t0011 | g0344 | AFR | ACB | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0329 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG03471 | hp2 | a0002 | c0015 | t0007 | g0246 | AFR | MSL | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG06807 | hp1 | a0001 | c0001 | t0011 | g0328 | AFR | USA | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0326 | AFR | USA | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA20300 | hp1 | a0002 | c0004 | t0016 | g0124 | AFR | USA | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA20300 | hp2 | a0001 | c0001 | t0046 | g0094 | AFR | USA | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA21309 | hp1 | a0001 | c0001 | t0012 | g0341 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0308 | AFR | LWK | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
homoSapiens | chm13v2 | a0001 | c0006 | t0001 | g0193 | REF | REF | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
homoSapiens | grch38p0 | a0001 | c0001 | t0012 | g0092 | REF | REF | CD82_chr11_44560663_44625358 | CD82 | chr11 | 44560663 | 44625358 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44615330 | G | T | 1 | a0003 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.395G>T | p.Arg132Leu | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/10 | 571/2212 | 395/804 | 132/267 | chr11 | 44615330 | |||
chr11:44618718 | A | G | 1 | a0002 | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
missense_variant | MODERATE | c.721A>G | p.Ile241Val | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/10 | 897/2212 | 721/804 | 241/267 | chr11 | 44618718 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44600202 | C | T | 1 | a0002c0026 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.108C>T | p.Ala36Ala | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/10 | 284/2212 | 108/804 | 36/267 | chr11 | 44600202 | |||
chr11:44605107 | G | A | 2 | a0001c0016 a0002c0019 |
4 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
synonymous_variant | LOW | c.186G>A | p.Val62Val | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 5/10 | 362/2212 | 186/804 | 62/267 | chr11 | 44605107 | |||
chr11:44605179 | G | T | 1 | a0001c0018 | 2 | HG01884.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.258G>T | p.Gly86Gly | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 5/10 | 434/2212 | 258/804 | 86/267 | chr11 | 44605179 | |||
chr11:44615283 | G | A | 8 | a0001c0006 a0001c0014 a0002c0002 others(5): Show |
100 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
synonymous_variant | LOW | c.348G>A | p.Glu116Glu | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/10 | 524/2212 | 348/804 | 116/267 | chr11 | 44615283 | |||
chr11:44615289 | C | T | 6 | a0001c0005 a0001c0009 a0002c0004 others(3): Show |
76 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(73): Show |
synonymous_variant | LOW | c.354C>T | p.Gly118Gly | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/10 | 530/2212 | 354/804 | 118/267 | chr11 | 44615289 | |||
chr11:44615298 | G | A | 3 | a0001c0011 a0001c0023 a0002c0017 |
15 | HG00673.hp2 NA18949.hp1 NA18950.hp2 others(12): Show |
synonymous_variant | LOW | c.363G>A | p.Val121Val | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/10 | 539/2212 | 363/804 | 121/267 | chr11 | 44615298 | |||
chr11:44618675 | G | A | 1 | a0002c0013 | 4 | HG00140.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
synonymous_variant | LOW | c.678G>A | p.Glu226Glu | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/10 | 854/2212 | 678/804 | 226/267 | chr11 | 44618675 | |||
chr11:44618696 | C | T | 1 | a0002c0025 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.699C>T | p.Gly233Gly | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/10 | 875/2212 | 699/804 | 233/267 | chr11 | 44618696 | |||
chr11:44618702 | C | T | 1 | a0002c0021 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.705C>T | p.Gly235Gly | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/10 | 881/2212 | 705/804 | 235/267 | chr11 | 44618702 | |||
chr11:44619066 | G | C | 2 | a0001c0012 a0002c0024 |
6 | HG02451.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.744G>C | p.Leu248Leu | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 920/2212 | 744/804 | 248/267 | chr11 | 44619066 | |||
chr11:44619090 | C | G | 9 | a0001c0005 a0001c0010 a0001c0014 others(6): Show |
69 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(66): Show |
synonymous_variant | LOW | c.768C>G | p.Val256Val | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 944/2212 | 768/804 | 256/267 | chr11 | 44619090 | |||
chr11:44619096 | C | T | 1 | a0002c0020 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.774C>T | p.Ser258Ser | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 950/2212 | 774/804 | 258/267 | chr11 | 44619096 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44587498 | C | T | 1 | a0001c0001t0051 | 1 | HG02258.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-79C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/10 | chr11 | 44587498 | |||||||
chr11:44619242 | T | C | 116 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(113): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
3_prime_UTR_variant | MODIFIER | c.*116T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 116 | chr11 | 44619242 | ||||||
chr11:44619243 | C | G | 16 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0014 others(13): Show |
24 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*117C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 117 | chr11 | 44619243 | ||||||
chr11:44619373 | A | C | 2 | a0002c0003t0041 a0002c0003t0042 |
2 | HG02145.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*247A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 247 | chr11 | 44619373 | ||||||
chr11:44619475 | G | A | 10 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0018 others(7): Show |
23 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*349G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 349 | chr11 | 44619475 | ||||||
chr11:44619484 | C | G | 1 | a0001c0010t0040 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*358C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 358 | chr11 | 44619484 | ||||||
chr11:44619485 | G | A | 1 | a0002c0002t0023 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*359G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 359 | chr11 | 44619485 | ||||||
chr11:44619489 | G | A | 3 | a0001c0001t0025 a0001c0001t0026 a0001c0006t0024 |
3 | HG03017.hp1 HG03710.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*363G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 363 | chr11 | 44619489 | ||||||
chr11:44619508 | A | G | 1 | a0002c0004t0039 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*382A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 382 | chr11 | 44619508 | ||||||
chr11:44619529 | G | A | 1 | a0001c0001t0027 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*403G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 403 | chr11 | 44619529 | ||||||
chr11:44619540 | A | G | 1 | a0002c0003t0038 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 414 | chr11 | 44619540 | ||||||
chr11:44619558 | C | T | 1 | a0001c0005t0037 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 432 | chr11 | 44619558 | ||||||
chr11:44619578 | T | C | 1 | a0002c0003t0043 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 452 | chr11 | 44619578 | ||||||
chr11:44619590 | G | A | 2 | a0002c0003t0028 a0002c0003t0044 |
2 | HG02145.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*464G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 464 | chr11 | 44619590 | ||||||
chr11:44619622 | G | A | 3 | a0002c0003t0029 a0002c0003t0030 a0002c0004t0009 |
7 | HG01496.hp1 HG02004.hp1 HG02293.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*496G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 496 | chr11 | 44619622 | ||||||
chr11:44619695 | C | T | 2 | a0002c0002t0020 a0002c0002t0036 |
3 | HG02015.hp1 HG02129.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*569C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 569 | chr11 | 44619695 | ||||||
chr11:44619724 | AC | A | 4 | a0001c0009t0010 a0002c0004t0035 a0002c0008t0010 others(1): Show |
6 | HG02135.hp2 HG02523.hp1 HG03831.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*599delC | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 599 | chr11 | 44619724 | ||||||
chr11:44619763 | C | CA | 28 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0017 others(25): Show |
52 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*663dupA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 664 | INFO_REALIGN_3_PRIME | chr11 | 44619763 | |||||
chr11:44619763 | C | CAA | 7 | a0001c0001t0007 a0001c0010t0007 a0001c0016t0048 others(4): Show |
9 | HG02257.hp2 HG02523.hp2 HG03098.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*663dupAA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 664 | INFO_REALIGN_3_PRIME | chr11 | 44619763 | |||||
chr11:44619763 | CA | C | 30 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0013 others(27): Show |
136 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*663delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 663 | INFO_REALIGN_3_PRIME | chr11 | 44619763 | |||||
chr11:44619763 | CAA | C | 24 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(21): Show |
79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*663delAA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 662 | INFO_REALIGN_3_PRIME | chr11 | 44619763 | |||||
chr11:44619806 | G | A | 1 | a0002c0015t0031 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 680 | chr11 | 44619806 | ||||||
chr11:44619872 | G | A | 1 | a0001c0010t0040 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*746G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 746 | chr11 | 44619872 | ||||||
chr11:44619873 | A | C | 1 | a0001c0010t0040 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*747A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 747 | chr11 | 44619873 | ||||||
chr11:44619935 | T | C | 1 | a0002c0002t0032 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*809T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 809 | chr11 | 44619935 | ||||||
chr11:44620029 | G | A | 2 | a0001c0001t0025 a0001c0001t0049 |
2 | HG02622.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*903G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 903 | chr11 | 44620029 | ||||||
chr11:44620034 | A | G | 7 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0046 others(4): Show |
9 | HG01243.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*908A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 908 | chr11 | 44620034 | ||||||
chr11:44620101 | A | G | 3 | a0001c0001t0018 a0002c0002t0022 a0002c0004t0018 |
3 | HG00099.hp1 HG02055.hp1 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*975A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 975 | chr11 | 44620101 | ||||||
chr11:44620181 | G | A | 1 | a0001c0005t0034 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 1055 | chr11 | 44620181 | ||||||
chr11:44620198 | G | A | 1 | a0002c0024t0047 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1072G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 1072 | chr11 | 44620198 | ||||||
chr11:44620279 | G | T | 10 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0013 others(7): Show |
26 | HG00621.hp1 HG00621.hp2 HG00741.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1153G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 1153 | chr11 | 44620279 | ||||||
chr11:44620353 | A | T | 1 | a0001c0010t0040 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1227A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 10/10 | 1227 | chr11 | 44620353 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44565814 | G | A | 5 | a0001c0001t0006g0016 a0001c0010t0002g0015 a0002c0003t0001g0012 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+78G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44565814 | |||||||
chr11:44565856 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(12): Show |
21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+120G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44565856 | |||||||
chr11:44565924 | C | T | 4 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0355 others(1): Show |
4 | HG02083.hp1 NA18950.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+188C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44565924 | |||||||
chr11:44566042 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(14): Show |
23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+306C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566042 | |||||||
chr11:44566044 | GA | G | 5 | a0001c0001t0006g0016 a0001c0010t0002g0015 a0002c0003t0001g0012 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+310delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44566044 | ||||||
chr11:44566198 | C | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(154): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.-103+462C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566198 | |||||||
chr11:44566290 | C | T | 1 | a0002c0003t0008g0349 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-103+554C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566290 | |||||||
chr11:44566337 | T | G | 1 | a0002c0002t0002g0224 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-103+601T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566337 | |||||||
chr11:44566449 | G | A | 35 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(32): Show |
35 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103+713G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566449 | |||||||
chr11:44566473 | A | G | 1 | a0002c0025t0004g0348 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-103+737A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566473 | |||||||
chr11:44566706 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(23): Show |
32 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.-103+970T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566706 | |||||||
chr11:44566707 | G | A | 5 | a0001c0001t0015g0259 a0001c0012t0004g0256 a0001c0012t0004g0257 others(2): Show |
5 | HG02451.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+971G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566707 | |||||||
chr11:44566740 | G | A | 62 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0307 others(59): Show |
63 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-103+1004G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566740 | |||||||
chr11:44566794 | C | CT | 8 | a0001c0001t0001g0314 a0001c0001t0001g0318 a0001c0001t0002g0316 others(5): Show |
8 | HG01074.hp2 HG01123.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-103+1068dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44566794 | ||||||
chr11:44566971 | A | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(12): Show |
21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+1235A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44566971 | |||||||
chr11:44567204 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(138): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-103+1468G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567204 | |||||||
chr11:44567603 | G | C | 1 | a0001c0001t0002g0266 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-103+1867G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567603 | |||||||
chr11:44567703 | C | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(13): Show |
22 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-103+1967C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567703 | |||||||
chr11:44567714 | C | T | 15 | a0001c0001t0005g0213 a0001c0001t0006g0214 a0001c0001t0013g0215 others(12): Show |
15 | HG00621.hp2 HG01175.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.-103+1978C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567714 | |||||||
chr11:44567729 | G | A | 10 | a0001c0001t0012g0341 a0001c0001t0049g0342 a0001c0006t0003g0343 others(7): Show |
10 | HG00639.hp2 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-103+1993G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567729 | |||||||
chr11:44567753 | G | A | 2 | a0001c0016t0017g0031 a0001c0016t0048g0032 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103+2017G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567753 | |||||||
chr11:44567884 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(14): Show |
23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+2148A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44567884 | |||||||
chr11:44568182 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-103+2446C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568182 | |||||||
chr11:44568291 | G | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(169): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-103+2555G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568291 | |||||||
chr11:44568353 | C | G | 6 | a0001c0001t0001g0331 a0001c0001t0007g0326 a0001c0001t0008g0329 others(3): Show |
6 | HG01884.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+2617C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568353 | |||||||
chr11:44568512 | T | A | 1 | a0001c0009t0001g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-103+2776T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568512 | |||||||
chr11:44568531 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(14): Show |
23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+2795A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568531 | |||||||
chr11:44568655 | T | C | 1 | a0001c0001t0027g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-103+2919T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568655 | |||||||
chr11:44568683 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(14): Show |
23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+2947C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568683 | |||||||
chr11:44568706 | G | A | 5 | a0001c0001t0001g0034 a0001c0016t0017g0031 a0001c0016t0048g0032 others(2): Show |
5 | HG02258.hp2 HG03195.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+2970G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568706 | |||||||
chr11:44568737 | G | A | 1 | a0001c0006t0001g0037 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-103+3001G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568737 | |||||||
chr11:44568776 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-103+3040G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568776 | |||||||
chr11:44568805 | C | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(14): Show |
23 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103+3069C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568805 | |||||||
chr11:44568884 | G | A | 1 | a0001c0001t0004g0332 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-103+3148G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44568884 | |||||||
chr11:44569023 | C | T | 1 | a0001c0001t0013g0221 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-103+3287C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569023 | |||||||
chr11:44569045 | G | A | 2 | a0001c0001t0051g0222 a0001c0009t0015g0223 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-103+3309G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569045 | |||||||
chr11:44569152 | A | G | 1 | a0001c0011t0005g0313 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-103+3416A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569152 | |||||||
chr11:44569161 | G | A | 7 | a0001c0001t0006g0016 a0001c0010t0001g0210 a0001c0010t0001g0211 others(4): Show |
7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-103+3425G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569161 | |||||||
chr11:44569168 | A | T | 2 | a0001c0001t0051g0222 a0001c0009t0015g0223 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-103+3432A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569168 | |||||||
chr11:44569179 | G | A | 146 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.-103+3443G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569179 | |||||||
chr11:44569310 | C | T | 2 | a0001c0005t0002g0208 a0001c0005t0003g0209 |
2 | NA18998.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-103+3574C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569310 | |||||||
chr11:44569323 | G | A | 3 | a0001c0018t0012g0268 a0002c0003t0008g0349 a0002c0003t0044g0267 |
3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+3587G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569323 | |||||||
chr11:44569340 | G | A | 1 | a0002c0004t0019g0040 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-103+3604G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569340 | |||||||
chr11:44569466 | T | C | 2 | a0002c0007t0002g0041 a0002c0007t0002g0042 |
2 | HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-103+3730T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569466 | |||||||
chr11:44569703 | T | G | 1 | a0002c0002t0003g0347 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-103+3967T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569703 | |||||||
chr11:44569748 | C | T | 1 | a0001c0001t0004g0038 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-103+4012C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569748 | |||||||
chr11:44569807 | G | C | 2 | a0002c0004t0002g0225 a0002c0004t0002g0226 |
2 | NA18954.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-103+4071G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569807 | |||||||
chr11:44569818 | G | A | 6 | a0001c0001t0012g0341 a0001c0001t0049g0342 a0001c0012t0003g0339 others(3): Show |
6 | HG02622.hp2 HG02717.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+4082G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569818 | |||||||
chr11:44569882 | A | T | 68 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0307 others(65): Show |
69 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-103+4146A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569882 | |||||||
chr11:44569954 | A | T | 1 | a0003c0022t0004g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-103+4218A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44569954 | |||||||
chr11:44570189 | C | T | 3 | a0001c0005t0001g0203 a0001c0005t0001g0204 a0001c0005t0002g0205 |
3 | HG00408.hp2 HG02129.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-103+4453C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570189 | |||||||
chr11:44570232 | CTGGCTGC others(43): Show |
C | 1 | a0001c0001t0004g0320 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-103+4549_-103+459 others(54): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44570232 | ||||||
chr11:44570273 | C | T | 20 | a0001c0001t0026g0117 a0001c0006t0001g0037 a0001c0006t0001g0164 others(17): Show |
20 | HG00609.hp1 HG00673.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-103+4537C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570273 | |||||||
chr11:44570469 | C | T | 1 | a0002c0004t0003g0202 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-103+4733C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570469 | |||||||
chr11:44570624 | G | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(164): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-103+4888G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570624 | |||||||
chr11:44570691 | GCTT | G | 7 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0002c0002t0001g0043 others(4): Show |
7 | HG01255.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103+4958_-103+496 others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44570691 | ||||||
chr11:44570707 | C | T | 3 | a0001c0012t0016g0312 a0002c0003t0041g0311 a0002c0003t0042g0310 |
3 | HG02145.hp2 HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-103+4971C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570707 | |||||||
chr11:44570719 | TTTA | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0021 others(217): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-103+4987_-103+498 others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44570719 | ||||||
chr11:44570728 | C | T | 1 | a0002c0002t0007g0029 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-103+4992C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570728 | |||||||
chr11:44570813 | G | C | 1 | a0002c0002t0003g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-103+5077G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44570813 | |||||||
chr11:44571052 | T | C | 6 | a0001c0001t0001g0331 a0001c0001t0007g0326 a0001c0001t0008g0329 others(3): Show |
6 | HG01884.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+5316T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571052 | |||||||
chr11:44571125 | G | A | 2 | a0001c0001t0004g0322 a0001c0001t0015g0351 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-103+5389G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571125 | |||||||
chr11:44571158 | G | A | 39 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(36): Show |
39 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-103+5422G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571158 | |||||||
chr11:44571189 | G | A | 1 | a0002c0008t0004g0090 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-103+5453G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571189 | |||||||
chr11:44571278 | C | G | 2 | a0001c0016t0004g0350 a0002c0003t0002g0039 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-103+5542C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571278 | |||||||
chr11:44571384 | A | G | 355 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(352): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-103+5648A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571384 | |||||||
chr11:44571405 | C | T | 7 | a0001c0001t0015g0259 a0001c0012t0004g0256 a0001c0012t0004g0257 others(4): Show |
7 | HG02055.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103+5669C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571405 | |||||||
chr11:44571479 | T | C | 2 | a0001c0001t0008g0265 a0001c0005t0001g0264 |
2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+5743T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571479 | |||||||
chr11:44571543 | A | G | 22 | a0001c0001t0005g0213 a0001c0001t0006g0016 a0001c0001t0006g0214 others(19): Show |
22 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-103+5807A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571543 | |||||||
chr11:44571655 | A | C | 2 | a0002c0003t0003g0255 a0002c0003t0004g0254 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-103+5919A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571655 | |||||||
chr11:44571866 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-103+6130G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571866 | |||||||
chr11:44571954 | C | A | 1 | a0001c0001t0003g0098 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-103+6218C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44571954 | |||||||
chr11:44572116 | G | A | 2 | a0001c0001t0008g0265 a0001c0005t0001g0264 |
2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+6380G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572116 | |||||||
chr11:44572238 | C | T | 3 | a0001c0018t0012g0268 a0002c0003t0008g0349 a0002c0003t0044g0267 |
3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+6502C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572238 | |||||||
chr11:44572256 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(164): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-103+6520C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572256 | |||||||
chr11:44572280 | G | A | 22 | a0001c0001t0005g0213 a0001c0001t0006g0016 a0001c0001t0006g0214 others(19): Show |
22 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-103+6544G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572280 | |||||||
chr11:44572283 | A | G | 2 | a0001c0001t0004g0322 a0001c0001t0015g0351 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-103+6547A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572283 | |||||||
chr11:44572334 | T | A | 39 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(36): Show |
39 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-103+6598T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572334 | |||||||
chr11:44572620 | CAA | C | 80 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0307 others(77): Show |
81 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-103+6885_-103+688 others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572620 | |||||||
chr11:44572810 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(164): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-103+7074T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572810 | |||||||
chr11:44572817 | T | TATGG | 59 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0307 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-103+7083_-103+708 others(8): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44572817 | ||||||
chr11:44572837 | C | A | 2 | a0001c0001t0008g0265 a0001c0005t0001g0264 |
2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+7101C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572837 | |||||||
chr11:44572841 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(166): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.-103+7105T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44572841 | |||||||
chr11:44572905 | CAG | C | 70 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0307 others(67): Show |
71 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103+7172_-103+717 others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44572905 | ||||||
chr11:44573004 | G | T | 3 | a0001c0001t0002g0200 a0001c0006t0003g0201 a0001c0014t0002g0199 |
3 | NA19012.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-103+7268G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573004 | |||||||
chr11:44573029 | C | T | 1 | a0002c0002t0003g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-103+7293C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573029 | |||||||
chr11:44573061 | T | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(103): Show |
113 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-103+7325T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573061 | |||||||
chr11:44573090 | G | A | 39 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(36): Show |
39 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-103+7354G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573090 | |||||||
chr11:44573127 | A | G | 1 | a0001c0001t0018g0198 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-103+7391A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573127 | |||||||
chr11:44573145 | T | A | 8 | a0001c0001t0001g0314 a0001c0001t0002g0266 a0001c0001t0003g0315 others(5): Show |
9 | HG00099.hp2 HG01123.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-103+7409T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573145 | |||||||
chr11:44573187 | G | C | 6 | a0001c0001t0001g0331 a0001c0001t0007g0326 a0001c0001t0008g0329 others(3): Show |
6 | HG01884.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+7451G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573187 | |||||||
chr11:44573190 | TATGTGTT others(17): Show |
T | 65 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(62): Show |
65 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-103+7456_-103+747 others(28): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44573190 | ||||||
chr11:44573241 | C | T | 2 | a0001c0001t0051g0222 a0001c0009t0015g0223 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-103+7505C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573241 | |||||||
chr11:44573300 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(12): Show |
21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+7564T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573300 | |||||||
chr11:44573384 | C | T | 13 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0004g0248 others(10): Show |
13 | HG02280.hp2 HG02486.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-103+7648C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573384 | |||||||
chr11:44573555 | T | A | 2 | a0001c0001t0008g0265 a0001c0005t0001g0264 |
2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+7819T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573555 | |||||||
chr11:44573556 | C | T | 2 | a0001c0001t0008g0265 a0001c0005t0001g0264 |
2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+7820C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573556 | |||||||
chr11:44573590 | G | A | 12 | a0001c0001t0003g0106 a0001c0005t0002g0208 a0001c0005t0003g0099 others(9): Show |
12 | HG02074.hp2 NA18949.hp2 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+7854G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573590 | |||||||
chr11:44573674 | T | C | 88 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0307 others(85): Show |
89 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-103+7938T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573674 | |||||||
chr11:44573899 | G | A | 6 | a0001c0001t0001g0331 a0001c0001t0007g0326 a0001c0001t0008g0329 others(3): Show |
6 | HG01884.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+8163G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44573899 | |||||||
chr11:44574091 | T | TG | 7 | a0001c0001t0015g0259 a0001c0012t0004g0256 a0001c0012t0004g0257 others(4): Show |
7 | HG02055.hp2 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103+8361dupG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44574091 | ||||||
chr11:44574144 | T | C | 1 | a0001c0001t0004g0332 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-103+8408T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574144 | |||||||
chr11:44574159 | G | C | 92 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0307 others(89): Show |
93 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.-103+8423G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574159 | |||||||
chr11:44574173 | G | C | 1 | a0002c0003t0028g0261 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-103+8437G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574173 | |||||||
chr11:44574212 | G | A | 2 | a0001c0001t0008g0265 a0001c0005t0001g0264 |
2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+8476G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574212 | |||||||
chr11:44574306 | G | A | 1 | a0001c0005t0002g0049 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-103+8570G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574306 | |||||||
chr11:44574319 | C | T | 91 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0307 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.-103+8583C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574319 | |||||||
chr11:44574416 | T | G | 91 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0307 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.-103+8680T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574416 | |||||||
chr11:44574486 | C | A | 7 | a0001c0001t0006g0016 a0001c0010t0001g0210 a0001c0010t0001g0211 others(4): Show |
7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-103+8750C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574486 | |||||||
chr11:44574606 | G | GT | 15 | a0001c0001t0001g0028 a0001c0001t0003g0309 a0001c0001t0004g0253 others(12): Show |
15 | HG01099.hp2 HG02055.hp1 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.-103+8878dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44574606 | ||||||
chr11:44574636 | C | T | 1 | a0001c0009t0011g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-103+8900C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574636 | |||||||
chr11:44574836 | C | G | 2 | a0001c0001t0008g0265 a0001c0005t0001g0264 |
2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103+9100C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574836 | |||||||
chr11:44574878 | G | A | 8 | a0001c0001t0001g0228 a0002c0002t0001g0232 a0002c0002t0003g0230 others(5): Show |
8 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-103+9142G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574878 | |||||||
chr11:44574952 | G | A | 1 | a0001c0001t0007g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-103+9216G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574952 | |||||||
chr11:44574974 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(12): Show |
21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+9238G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44574974 | |||||||
chr11:44575035 | G | A | 3 | a0001c0012t0004g0256 a0001c0012t0004g0257 a0002c0003t0014g0258 |
3 | HG02451.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-103+9299G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575035 | |||||||
chr11:44575267 | A | G | 36 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(33): Show |
36 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103+9531A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575267 | |||||||
chr11:44575358 | C | T | 1 | a0001c0001t0008g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-103+9622C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575358 | |||||||
chr11:44575407 | G | A | 1 | a0002c0002t0023g0108 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-103+9671G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575407 | |||||||
chr11:44575452 | ACT | A | 9 | a0001c0001t0008g0265 a0001c0001t0051g0222 a0001c0005t0001g0264 others(6): Show |
9 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-103+9719_-103+972 others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44575452 | ||||||
chr11:44575601 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(12): Show |
21 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-103+9865G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575601 | |||||||
chr11:44575746 | T | C | 1 | a0001c0009t0001g0087 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-103+10010T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575746 | |||||||
chr11:44575998 | A | C | 3 | a0001c0018t0012g0268 a0002c0003t0008g0349 a0002c0003t0044g0267 |
3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+10262A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44575998 | |||||||
chr11:44576028 | G | A | 3 | a0001c0018t0012g0268 a0002c0003t0008g0349 a0002c0003t0044g0267 |
3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+10292G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576028 | |||||||
chr11:44576335 | G | C | 1 | a0002c0002t0003g0109 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-103+10599G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576335 | |||||||
chr11:44576397 | C | T | 3 | a0001c0018t0012g0268 a0002c0003t0008g0349 a0002c0003t0044g0267 |
3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+10661C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576397 | |||||||
chr11:44576530 | C | T | 3 | a0001c0018t0012g0268 a0002c0003t0008g0349 a0002c0003t0044g0267 |
3 | HG01884.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-103+10794C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576530 | |||||||
chr11:44576532 | G | A | 24 | a0001c0001t0001g0034 a0001c0001t0003g0110 a0001c0001t0005g0213 others(21): Show |
24 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-103+10796G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576532 | |||||||
chr11:44576553 | A | G | 1 | a0001c0012t0004g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-103+10817A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576553 | |||||||
chr11:44576602 | G | A | 4 | a0001c0001t0004g0332 a0001c0001t0015g0259 a0001c0001t0015g0262 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+10866G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576602 | |||||||
chr11:44576685 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(172): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-102-10790A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576685 | |||||||
chr11:44576753 | A | G | 1 | a0001c0006t0003g0192 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-102-10722A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576753 | |||||||
chr11:44576773 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(172): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-102-10702T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576773 | |||||||
chr11:44576845 | T | G | 4 | a0001c0012t0004g0256 a0001c0012t0004g0257 a0002c0003t0014g0258 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-10630T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576845 | |||||||
chr11:44576868 | G | A | 35 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(32): Show |
35 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-102-10607G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576868 | |||||||
chr11:44576886 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
284 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.-102-10589A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576886 | |||||||
chr11:44576887 | G | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(198): Show |
203 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-102-10588G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576887 | |||||||
chr11:44576963 | G | T | 1 | a0002c0007t0004g0346 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-102-10512G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44576963 | |||||||
chr11:44577083 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-102-10392C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577083 | |||||||
chr11:44577084 | G | T | 1 | a0001c0001t0001g0307 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-102-10391G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577084 | |||||||
chr11:44577100 | C | A | 2 | a0001c0001t0004g0322 a0001c0001t0015g0351 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-102-10375C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577100 | |||||||
chr11:44577206 | A | G | 1 | a0002c0003t0001g0086 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-102-10269A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577206 | |||||||
chr11:44577224 | G | A | 2 | a0001c0016t0017g0031 a0001c0016t0048g0032 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-102-10251G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577224 | |||||||
chr11:44577464 | C | T | 3 | a0001c0016t0004g0350 a0002c0003t0002g0039 a0002c0017t0001g0191 |
3 | HG02055.hp2 NA19067.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-102-10011C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577464 | |||||||
chr11:44577525 | C | T | 2 | a0001c0001t0046g0094 a0002c0003t0001g0093 |
2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-102-9950C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577525 | |||||||
chr11:44577658 | G | A | 1 | a0002c0003t0044g0267 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-102-9817G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577658 | |||||||
chr11:44577676 | T | C | 12 | a0001c0001t0003g0110 a0001c0001t0006g0016 a0001c0010t0001g0210 others(9): Show |
12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-9799T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577676 | |||||||
chr11:44577818 | A | G | 1 | a0001c0001t0018g0198 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-102-9657A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577818 | |||||||
chr11:44577828 | G | A | 1 | a0002c0007t0002g0050 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-102-9647G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577828 | |||||||
chr11:44577894 | G | A | 1 | a0001c0001t0007g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-102-9581G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577894 | |||||||
chr11:44577993 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(20): Show |
29 | HG00423.hp1 HG00621.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-102-9482C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44577993 | |||||||
chr11:44578110 | G | A | 1 | a0002c0008t0002g0111 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-102-9365G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578110 | |||||||
chr11:44578213 | AC | A | 12 | a0001c0001t0003g0110 a0001c0001t0006g0016 a0001c0010t0001g0210 others(9): Show |
12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-9259delC | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44578213 | ||||||
chr11:44578285 | G | A | 1 | a0002c0002t0003g0051 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-102-9190G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578285 | |||||||
chr11:44578560 | A | G | 9 | a0001c0001t0004g0096 a0001c0001t0004g0322 a0001c0001t0015g0351 others(6): Show |
9 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-102-8915A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578560 | |||||||
chr11:44578660 | C | T | 3 | a0001c0012t0016g0312 a0002c0003t0041g0311 a0002c0003t0042g0310 |
3 | HG02145.hp2 HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-102-8815C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578660 | |||||||
chr11:44578742 | C | T | 8 | a0001c0001t0001g0034 a0001c0011t0001g0333 a0001c0011t0001g0335 others(5): Show |
8 | NA18942.hp2 NA18965.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-102-8733C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578742 | |||||||
chr11:44578900 | T | C | 2 | a0002c0015t0003g0338 a0002c0025t0004g0348 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-102-8575T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44578900 | |||||||
chr11:44579053 | A | G | 1 | a0002c0015t0003g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-102-8422A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579053 | |||||||
chr11:44579104 | A | G | 8 | a0001c0001t0003g0110 a0001c0001t0006g0016 a0001c0010t0001g0210 others(5): Show |
8 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-102-8371A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579104 | |||||||
chr11:44579147 | T | A | 1 | a0002c0003t0001g0086 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-102-8328T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579147 | |||||||
chr11:44579168 | A | G | 12 | a0001c0001t0003g0110 a0001c0001t0006g0016 a0001c0010t0001g0210 others(9): Show |
12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-8307A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579168 | |||||||
chr11:44579183 | G | A | 12 | a0001c0001t0003g0110 a0001c0001t0006g0016 a0001c0010t0001g0210 others(9): Show |
12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-8292G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579183 | |||||||
chr11:44579240 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(169): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-102-8235A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579240 | |||||||
chr11:44579256 | G | T | 1 | a0002c0002t0001g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-102-8219G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579256 | |||||||
chr11:44579285 | G | A | 8 | a0001c0001t0003g0110 a0001c0001t0006g0016 a0001c0010t0001g0210 others(5): Show |
8 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-102-8190G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579285 | |||||||
chr11:44579290 | T | C | 12 | a0001c0001t0003g0110 a0001c0001t0006g0016 a0001c0010t0001g0210 others(9): Show |
12 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-8185T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579290 | |||||||
chr11:44579426 | G | A | 1 | a0001c0001t0027g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-102-8049G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579426 | |||||||
chr11:44579433 | C | A | 2 | a0001c0001t0001g0228 a0002c0004t0002g0227 |
2 | HG01167.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-102-8042C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579433 | |||||||
chr11:44579493 | G | A | 36 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0242 others(33): Show |
36 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-102-7982G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579493 | |||||||
chr11:44579564 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(181): Show |
186 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-102-7911C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579564 | |||||||
chr11:44579619 | G | A | 1 | a0001c0001t0014g0212 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-102-7856G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579619 | |||||||
chr11:44579638 | C | T | 1 | a0002c0003t0004g0345 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-102-7837C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579638 | |||||||
chr11:44579710 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(29): Show |
38 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-102-7765G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579710 | |||||||
chr11:44579713 | G | A | 3 | a0001c0006t0001g0037 a0002c0002t0002g0112 a0002c0002t0002g0113 |
3 | HG00609.hp1 HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-102-7762G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579713 | |||||||
chr11:44579736 | G | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0059 others(19): Show |
24 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-102-7739G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579736 | |||||||
chr11:44579949 | A | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(181): Show |
186 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-102-7526A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44579949 | |||||||
chr11:44580406 | G | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(182): Show |
187 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-102-7069G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580406 | |||||||
chr11:44580457 | G | C | 1 | a0001c0005t0003g0099 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-102-7018G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580457 | |||||||
chr11:44580542 | G | A | 1 | a0001c0005t0003g0099 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-102-6933G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580542 | |||||||
chr11:44580788 | G | A | 16 | a0001c0001t0001g0034 a0001c0001t0005g0213 a0001c0001t0006g0214 others(13): Show |
16 | HG00621.hp2 HG01175.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.-102-6687G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580788 | |||||||
chr11:44580885 | C | T | 1 | a0001c0001t0027g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-102-6590C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580885 | |||||||
chr11:44580891 | G | C | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(353): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-102-6584G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580891 | |||||||
chr11:44580928 | G | T | 1 | a0001c0001t0007g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-102-6547G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44580928 | |||||||
chr11:44581066 | T | C | 1 | a0002c0002t0001g0043 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-102-6409T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581066 | |||||||
chr11:44581157 | G | C | 1 | a0002c0004t0009g0236 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-102-6318G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581157 | |||||||
chr11:44581231 | G | A | 16 | a0001c0001t0001g0034 a0001c0001t0005g0213 a0001c0001t0006g0214 others(13): Show |
16 | HG00621.hp2 HG01175.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.-102-6244G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581231 | |||||||
chr11:44581378 | A | C | 2 | a0001c0016t0004g0350 a0002c0003t0002g0039 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-102-6097A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581378 | |||||||
chr11:44581425 | T | C | 2 | a0001c0016t0004g0350 a0002c0003t0002g0039 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-102-6050T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581425 | |||||||
chr11:44581704 | C | T | 2 | a0001c0009t0004g0085 a0002c0004t0003g0202 |
2 | HG02630.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-102-5771C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581704 | |||||||
chr11:44581730 | T | A | 1 | a0001c0001t0027g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-102-5745T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581730 | |||||||
chr11:44581778 | A | G | 257 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0045 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.-102-5697A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581778 | |||||||
chr11:44581796 | C | G | 1 | a0001c0005t0002g0189 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-102-5679C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581796 | |||||||
chr11:44581913 | G | A | 3 | a0001c0006t0001g0120 a0001c0006t0002g0121 a0001c0010t0001g0122 |
3 | HG00438.hp1 HG02135.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.-102-5562G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44581913 | |||||||
chr11:44582047 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(251): Show |
256 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-102-5428T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582047 | |||||||
chr11:44582059 | G | T | 31 | a0001c0001t0001g0331 a0001c0001t0004g0096 a0001c0001t0004g0322 others(28): Show |
31 | HG00639.hp2 HG01109.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.-102-5416G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582059 | |||||||
chr11:44582073 | G | A | 5 | a0001c0010t0008g0247 a0002c0003t0003g0255 a0002c0003t0004g0251 others(2): Show |
5 | HG02280.hp2 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-5402G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582073 | |||||||
chr11:44582088 | A | G | 4 | a0001c0012t0004g0256 a0001c0012t0004g0257 a0002c0003t0014g0258 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-5387A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582088 | |||||||
chr11:44582157 | G | A | 2 | a0002c0003t0001g0005 a0002c0003t0003g0005 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-102-5318G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582157 | |||||||
chr11:44582194 | T | TG | 350 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(347): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-102-5277dupG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44582194 | ||||||
chr11:44582231 | C | T | 2 | a0001c0005t0001g0204 a0001c0005t0002g0205 |
2 | HG00408.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-102-5244C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582231 | |||||||
chr11:44582271 | G | A | 7 | a0001c0001t0004g0096 a0001c0010t0004g0095 a0001c0010t0007g0097 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102-5204G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582271 | |||||||
chr11:44582341 | C | T | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(231): Show |
236 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-102-5134C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582341 | |||||||
chr11:44582345 | G | A | 1 | a0002c0003t0001g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-102-5130G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582345 | |||||||
chr11:44582462 | G | T | 1 | a0001c0009t0002g0186 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-102-5013G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582462 | |||||||
chr11:44582490 | C | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0052 others(114): Show |
119 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-102-4985C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582490 | |||||||
chr11:44582590 | A | G | 5 | a0001c0001t0001g0318 a0002c0003t0002g0305 a0002c0003t0003g0319 others(2): Show |
5 | HG01074.hp2 HG01346.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-4885A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582590 | |||||||
chr11:44582606 | G | A | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-102-4869G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582606 | |||||||
chr11:44582614 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-102-4861A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582614 | |||||||
chr11:44582631 | A | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(316): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-102-4844A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582631 | |||||||
chr11:44582750 | C | G | 1 | a0001c0010t0007g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-102-4725C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582750 | |||||||
chr11:44582801 | G | A | 24 | a0001c0001t0001g0034 a0001c0001t0003g0110 a0001c0001t0005g0213 others(21): Show |
24 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-102-4674G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582801 | |||||||
chr11:44582997 | A | G | 1 | a0002c0003t0011g0260 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-102-4478A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44582997 | |||||||
chr11:44583096 | C | T | 1 | a0002c0003t0001g0116 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-102-4379C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583096 | |||||||
chr11:44583186 | A | C | 5 | a0001c0001t0001g0331 a0001c0001t0008g0271 a0001c0001t0008g0329 others(2): Show |
5 | HG03041.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-4289A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583186 | |||||||
chr11:44583250 | G | C | 1 | a0001c0005t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-102-4225G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583250 | |||||||
chr11:44583473 | C | A | 3 | a0001c0005t0003g0099 a0002c0002t0001g0100 a0002c0002t0003g0101 |
3 | NA18949.hp2 NA19011.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-102-4002C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583473 | |||||||
chr11:44583666 | C | T | 1 | a0001c0014t0002g0026 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-102-3809C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583666 | |||||||
chr11:44583722 | T | C | 3 | a0001c0012t0004g0256 a0001c0012t0004g0257 a0002c0015t0007g0246 |
3 | HG02451.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-102-3753T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583722 | |||||||
chr11:44583751 | A | G | 1 | a0001c0005t0003g0209 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-102-3724A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583751 | |||||||
chr11:44583762 | G | A | 3 | a0001c0001t0016g0125 a0001c0012t0004g0194 a0002c0004t0016g0124 |
3 | HG01243.hp2 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-102-3713G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583762 | |||||||
chr11:44583785 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0045 others(222): Show |
226 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-102-3690A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583785 | |||||||
chr11:44583912 | A | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0065 others(90): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-102-3563A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583912 | |||||||
chr11:44583917 | G | A | 24 | a0001c0001t0001g0034 a0001c0001t0003g0110 a0001c0001t0005g0213 others(21): Show |
24 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-102-3558G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583917 | |||||||
chr11:44583955 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-102-3520G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583955 | |||||||
chr11:44583967 | A | G | 1 | a0002c0004t0002g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-102-3508A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583967 | |||||||
chr11:44583981 | C | T | 27 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0003g0110 others(24): Show |
27 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-102-3494C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44583981 | |||||||
chr11:44584030 | A | G | 1 | a0001c0005t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-102-3445A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584030 | |||||||
chr11:44584076 | A | T | 6 | a0001c0005t0001g0088 a0001c0005t0002g0080 a0001c0005t0037g0083 others(3): Show |
6 | NA18942.hp1 NA18948.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102-3399A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584076 | |||||||
chr11:44584223 | T | A | 346 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(343): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.-102-3252T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584223 | |||||||
chr11:44584405 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0052 |
3 | HG01256.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-102-3070G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584405 | |||||||
chr11:44584438 | C | T | 3 | a0001c0001t0004g0332 a0001c0001t0012g0084 a0002c0007t0004g0346 |
3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-102-3037C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584438 | |||||||
chr11:44584668 | A | T | 1 | a0001c0009t0002g0184 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-102-2807A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584668 | |||||||
chr11:44584668 | AT | A | 25 | a0001c0001t0001g0034 a0001c0001t0003g0110 a0001c0001t0005g0213 others(22): Show |
25 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-102-2796delT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44584668 | ||||||
chr11:44584999 | G | A | 3 | a0001c0005t0002g0290 a0001c0005t0002g0291 a0001c0009t0011g0263 |
3 | HG02486.hp1 NA18939.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-102-2476G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44584999 | |||||||
chr11:44585387 | A | G | 1 | a0001c0001t0046g0094 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-102-2088A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585387 | |||||||
chr11:44585555 | G | A | 3 | a0001c0001t0004g0332 a0001c0001t0012g0084 a0002c0007t0004g0346 |
3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-102-1920G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585555 | |||||||
chr11:44585652 | C | T | 1 | a0002c0002t0036g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-102-1823C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585652 | |||||||
chr11:44585731 | C | T | 36 | a0001c0001t0001g0065 a0001c0001t0001g0241 a0001c0001t0001g0242 others(33): Show |
36 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.-102-1744C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585731 | |||||||
chr11:44585781 | G | A | 1 | a0002c0002t0001g0126 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-102-1694G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585781 | |||||||
chr11:44585782 | T | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(166): Show |
171 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-102-1693T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585782 | |||||||
chr11:44585856 | C | T | 4 | a0001c0001t0004g0332 a0001c0001t0012g0084 a0001c0009t0001g0087 others(1): Show |
4 | HG02451.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-1619C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585856 | |||||||
chr11:44585860 | G | A | 1 | a0002c0003t0001g0027 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-102-1615G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585860 | |||||||
chr11:44585881 | T | C | 1 | a0002c0003t0014g0258 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-102-1594T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585881 | |||||||
chr11:44585921 | G | A | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-102-1554G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585921 | |||||||
chr11:44585981 | C | T | 3 | a0001c0012t0004g0256 a0001c0012t0004g0257 a0002c0015t0007g0246 |
3 | HG02451.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-102-1494C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585981 | |||||||
chr11:44585982 | G | A | 1 | a0002c0002t0004g0127 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-102-1493G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44585982 | |||||||
chr11:44586277 | C | T | 1 | a0001c0005t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-102-1198C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586277 | |||||||
chr11:44586288 | T | TGGG | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-102-1185_-102-118 others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 44586288 | ||||||
chr11:44586299 | A | T | 23 | a0001c0001t0001g0034 a0001c0001t0003g0110 a0001c0001t0005g0213 others(20): Show |
23 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-102-1176A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586299 | |||||||
chr11:44586340 | T | C | 41 | a0001c0001t0001g0065 a0001c0001t0001g0241 a0001c0001t0001g0242 others(38): Show |
41 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-102-1135T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586340 | |||||||
chr11:44586357 | A | G | 1 | a0001c0001t0003g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-102-1118A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586357 | |||||||
chr11:44586417 | C | G | 1 | a0001c0001t0003g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-102-1058C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586417 | |||||||
chr11:44586482 | G | A | 41 | a0001c0001t0001g0065 a0001c0001t0001g0241 a0001c0001t0001g0242 others(38): Show |
41 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-102-993G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586482 | |||||||
chr11:44586525 | G | A | 3 | a0001c0001t0004g0332 a0001c0001t0012g0084 a0002c0007t0004g0346 |
3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-102-950G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586525 | |||||||
chr11:44586728 | G | A | 2 | a0001c0001t0001g0314 a0001c0001t0003g0315 |
2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-102-747G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586728 | |||||||
chr11:44586885 | C | G | 1 | a0001c0001t0006g0016 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-102-590C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586885 | |||||||
chr11:44586936 | G | C | 1 | a0001c0001t0017g0283 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-102-539G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44586936 | |||||||
chr11:44587013 | C | T | 38 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0286 others(35): Show |
38 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.-102-462C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587013 | |||||||
chr11:44587055 | C | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(269): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.-102-420C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587055 | |||||||
chr11:44587180 | G | A | 2 | a0001c0009t0001g0178 a0002c0004t0003g0070 |
2 | HG01123.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-102-295G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587180 | |||||||
chr11:44587217 | C | T | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-102-258C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587217 | |||||||
chr11:44587272 | A | G | 10 | a0001c0001t0004g0096 a0001c0010t0004g0095 a0001c0010t0007g0097 others(7): Show |
10 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-102-203A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587272 | |||||||
chr11:44587286 | C | T | 3 | a0001c0001t0004g0332 a0001c0001t0012g0084 a0002c0007t0004g0346 |
3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-102-189C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587286 | |||||||
chr11:44587316 | T | C | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-102-159T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587316 | |||||||
chr11:44587330 | G | A | 8 | a0001c0001t0004g0322 a0001c0010t0008g0247 a0002c0003t0003g0255 others(5): Show |
8 | HG02280.hp2 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-102-145G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587330 | |||||||
chr11:44587385 | G | A | 1 | a0001c0001t0004g0308 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-102-90G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 1/9 | chr11 | 44587385 | |||||||
chr11:44587579 | T | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0140 others(169): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-21+23T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587579 | |||||||
chr11:44587595 | A | G | 1 | a0002c0002t0003g0174 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-21+39A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587595 | |||||||
chr11:44587631 | G | A | 1 | a0001c0005t0002g0208 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-21+75G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587631 | |||||||
chr11:44587648 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(259): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.-21+92G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587648 | |||||||
chr11:44587799 | C | G | 26 | a0001c0001t0001g0034 a0001c0001t0003g0110 a0001c0001t0004g0332 others(23): Show |
26 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-21+243C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587799 | |||||||
chr11:44587851 | C | T | 9 | a0001c0001t0004g0096 a0001c0010t0004g0095 a0001c0010t0007g0097 others(6): Show |
9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+295C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44587851 | |||||||
chr11:44588000 | G | T | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-21+444G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588000 | |||||||
chr11:44588007 | T | C | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-21+451T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588007 | |||||||
chr11:44588033 | C | T | 2 | a0001c0005t0002g0208 a0001c0005t0003g0209 |
2 | NA18998.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-21+477C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588033 | |||||||
chr11:44588034 | G | A | 1 | a0002c0003t0042g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-21+478G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588034 | |||||||
chr11:44588124 | A | G | 37 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0286 others(34): Show |
37 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-21+568A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588124 | |||||||
chr11:44588205 | T | TG | 130 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0140 others(127): Show |
130 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-21+653dupG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44588205 | ||||||
chr11:44588209 | G | GT | 190 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0048 others(187): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-21+663dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44588209 | ||||||
chr11:44588220 | G | T | 1 | a0002c0003t0004g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-21+664G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588220 | |||||||
chr11:44588222 | T | G | 1 | a0002c0003t0004g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-21+666T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588222 | |||||||
chr11:44588234 | G | GT | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(275): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-21+686dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44588234 | ||||||
chr11:44588254 | C | T | 3 | a0001c0001t0004g0332 a0001c0001t0012g0084 a0002c0007t0004g0346 |
3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-21+698C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588254 | |||||||
chr11:44588287 | G | A | 8 | a0001c0001t0004g0096 a0001c0010t0004g0095 a0001c0016t0017g0031 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+731G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588287 | |||||||
chr11:44588465 | G | A | 1 | a0002c0024t0047g0282 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-21+909G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588465 | |||||||
chr11:44588514 | A | T | 37 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0286 others(34): Show |
37 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-21+958A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588514 | |||||||
chr11:44588738 | G | A | 1 | a0002c0008t0001g0129 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-21+1182G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588738 | |||||||
chr11:44588809 | T | C | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-21+1253T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588809 | |||||||
chr11:44588870 | T | C | 12 | a0001c0001t0001g0065 a0001c0001t0004g0096 a0001c0010t0004g0095 others(9): Show |
12 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-21+1314T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588870 | |||||||
chr11:44588902 | C | G | 1 | a0002c0003t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-21+1346C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588902 | |||||||
chr11:44588904 | T | A | 1 | a0002c0003t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-21+1348T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588904 | |||||||
chr11:44588994 | C | T | 9 | a0001c0001t0004g0096 a0001c0010t0004g0095 a0001c0010t0007g0097 others(6): Show |
9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+1438C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44588994 | |||||||
chr11:44589049 | G | C | 23 | a0001c0001t0001g0034 a0001c0001t0003g0110 a0001c0001t0005g0213 others(20): Show |
23 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21+1493G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589049 | |||||||
chr11:44589112 | C | T | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(271): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.-21+1556C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589112 | |||||||
chr11:44589117 | A | G | 3 | a0001c0001t0001g0065 a0002c0003t0001g0093 a0002c0015t0007g0246 |
3 | HG02109.hp1 HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+1561A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589117 | |||||||
chr11:44589227 | G | C | 23 | a0001c0001t0001g0034 a0001c0001t0003g0110 a0001c0001t0005g0213 others(20): Show |
23 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21+1671G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589227 | |||||||
chr11:44589241 | G | A | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(271): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.-21+1685G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589241 | |||||||
chr11:44589277 | CA | C | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0004g0248 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+1722delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589277 | |||||||
chr11:44589449 | A | C | 1 | a0001c0001t0014g0212 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-21+1893A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589449 | |||||||
chr11:44589517 | C | T | 1 | a0001c0001t0049g0342 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-21+1961C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589517 | |||||||
chr11:44589629 | G | A | 1 | a0002c0015t0007g0246 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-21+2073G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589629 | |||||||
chr11:44589697 | G | A | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0004g0248 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+2141G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589697 | |||||||
chr11:44589818 | G | C | 3 | a0001c0001t0004g0332 a0001c0001t0012g0084 a0002c0007t0004g0346 |
3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-21+2262G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589818 | |||||||
chr11:44589887 | G | A | 2 | a0001c0016t0017g0031 a0001c0016t0048g0032 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-21+2331G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589887 | |||||||
chr11:44589896 | C | T | 1 | a0001c0001t0003g0303 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-21+2340C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589896 | |||||||
chr11:44589942 | T | C | 9 | a0001c0001t0004g0096 a0001c0010t0004g0095 a0001c0010t0007g0097 others(6): Show |
9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+2386T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589942 | |||||||
chr11:44589994 | T | C | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(280): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-21+2438T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44589994 | |||||||
chr11:44590034 | C | T | 9 | a0001c0001t0004g0096 a0001c0010t0004g0095 a0001c0010t0007g0097 others(6): Show |
9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+2478C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590034 | |||||||
chr11:44590063 | C | G | 26 | a0001c0001t0001g0034 a0001c0001t0003g0110 a0001c0001t0004g0332 others(23): Show |
26 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-21+2507C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590063 | |||||||
chr11:44590119 | C | T | 346 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(343): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.-21+2563C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590119 | |||||||
chr11:44590183 | C | T | 1 | a0001c0010t0008g0247 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-21+2627C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590183 | |||||||
chr11:44590191 | G | A | 3 | a0001c0001t0004g0332 a0001c0001t0012g0084 a0002c0007t0004g0346 |
3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-21+2635G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590191 | |||||||
chr11:44590230 | A | AG | 323 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(320): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-21+2676dupG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590230 | ||||||
chr11:44590475 | G | C | 3 | a0001c0001t0001g0065 a0002c0003t0001g0093 a0002c0015t0007g0246 |
3 | HG02109.hp1 HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+2919G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590475 | |||||||
chr11:44590543 | G | A | 2 | a0001c0012t0004g0256 a0001c0012t0004g0257 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-21+2987G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590543 | |||||||
chr11:44590610 | C | CAAAAA | 14 | a0001c0001t0003g0175 a0001c0001t0004g0176 a0001c0001t0004g0177 others(11): Show |
14 | HG00639.hp2 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.-21+3070_-21+3074d others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAA | 12 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0004g0253 others(9): Show |
12 | HG01884.hp1 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-21+3069_-21+3074d others(8): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA | 60 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0061 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-21+3068_-21+3074d others(9): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(1): Show |
17 | a0001c0001t0001g0008 a0001c0001t0001g0314 a0001c0001t0001g0318 others(14): Show |
17 | HG00735.hp1 HG01243.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21+3067_-21+3074d others(10): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(2): Show |
12 | a0001c0001t0002g0172 a0001c0001t0004g0096 a0001c0005t0037g0083 others(9): Show |
12 | HG02132.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21+3066_-21+3074d others(11): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(3): Show |
52 | a0001c0001t0002g0200 a0001c0001t0013g0072 a0001c0005t0001g0203 others(49): Show |
53 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-21+3065_-21+3074d others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(4): Show |
97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(94): Show |
98 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-21+3064_-21+3074d others(13): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(5): Show |
32 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0307 others(29): Show |
32 | HG00099.hp1 HG00544.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-21+3063_-21+3074d others(14): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(6): Show |
13 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0002c0002t0003g0089 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-21+3062_-21+3074d others(15): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(7): Show |
4 | a0001c0009t0004g0238 a0002c0004t0002g0225 a0002c0004t0002g0226 others(1): Show |
4 | HG00609.hp2 HG01891.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+3061_-21+3074d others(16): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(8): Show |
2 | a0001c0005t0002g0182 a0001c0010t0003g0237 |
2 | HG00558.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.-21+3060_-21+3074d others(17): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(13): Show |
7 | a0001c0001t0001g0065 a0001c0001t0013g0215 a0001c0001t0013g0221 others(4): Show |
7 | HG00621.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+3055_-21+3074d others(22): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(14): Show |
10 | a0001c0001t0006g0214 a0001c0010t0001g0211 a0001c0010t0002g0015 others(7): Show |
10 | HG00639.hp1 HG01192.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+3074_-21+3075i others(23): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0034 a0001c0010t0001g0210 a0001c0011t0001g0333 |
3 | HG01106.hp2 NA18970.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-21+3074_-21+3075i others(24): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(16): Show |
2 | a0002c0007t0002g0013 a0002c0007t0002g0014 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-21+3074_-21+3075i others(25): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(17): Show |
3 | a0001c0001t0005g0213 a0001c0001t0006g0016 a0002c0003t0001g0012 |
3 | HG01175.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-21+3074_-21+3075i others(26): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590610 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0003g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-21+3074_-21+3075i others(27): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590610 | ||||||
chr11:44590642 | T | TTCTTAGC others(139): Show |
3 | a0001c0005t0002g0182 a0001c0009t0004g0238 a0001c0010t0003g0237 |
3 | HG00558.hp1 HG00609.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-21+3087_-21+3232d others(148): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44590642 | ||||||
chr11:44590732 | T | C | 1 | a0001c0016t0004g0350 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-21+3176T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590732 | |||||||
chr11:44590803 | C | G | 47 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0061 others(44): Show |
48 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+3247C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590803 | |||||||
chr11:44590909 | G | A | 1 | a0001c0001t0014g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-21+3353G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590909 | |||||||
chr11:44590957 | C | T | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-21+3401C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590957 | |||||||
chr11:44590984 | C | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0059 others(70): Show |
74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-21+3428C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44590984 | |||||||
chr11:44591098 | C | T | 1 | a0002c0003t0005g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-21+3542C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591098 | |||||||
chr11:44591125 | T | A | 3 | a0001c0006t0002g0162 a0001c0006t0003g0201 a0001c0014t0002g0199 |
3 | NA18959.hp1 NA19012.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-20-3518T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591125 | |||||||
chr11:44591164 | C | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(168): Show |
173 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-20-3479C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591164 | |||||||
chr11:44591186 | G | A | 3 | a0001c0001t0006g0011 a0002c0003t0045g0066 a0002c0015t0003g0338 |
4 | HG01257.hp2 HG01258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-3457G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591186 | |||||||
chr11:44591243 | G | A | 9 | a0001c0001t0004g0096 a0001c0010t0004g0095 a0001c0010t0007g0097 others(6): Show |
9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20-3400G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591243 | |||||||
chr11:44591260 | C | T | 2 | a0002c0004t0001g0009 a0002c0004t0002g0009 |
2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.-20-3383C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591260 | |||||||
chr11:44591425 | C | A | 1 | a0001c0005t0002g0049 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-20-3218C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591425 | |||||||
chr11:44591833 | A | AT | 306 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(303): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-20-2802dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44591833 | ||||||
chr11:44591842 | G | C | 2 | a0001c0012t0004g0256 a0001c0012t0004g0257 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-20-2801G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591842 | |||||||
chr11:44591850 | G | T | 1 | a0002c0002t0001g0171 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-20-2793G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591850 | |||||||
chr11:44591893 | C | T | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0004g0248 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2750C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44591893 | |||||||
chr11:44592121 | T | C | 60 | a0001c0001t0001g0034 a0001c0001t0001g0241 a0001c0001t0001g0242 others(57): Show |
60 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.-20-2522T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592121 | |||||||
chr11:44592170 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0140 others(102): Show |
105 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-20-2473G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592170 | |||||||
chr11:44592239 | C | T | 1 | a0001c0005t0002g0189 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-20-2404C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592239 | |||||||
chr11:44592430 | C | T | 2 | a0001c0001t0008g0265 a0001c0001t0015g0351 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-20-2213C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592430 | |||||||
chr11:44592455 | G | C | 1 | a0002c0002t0003g0166 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-20-2188G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592455 | |||||||
chr11:44592480 | G | T | 3 | a0001c0001t0004g0332 a0001c0001t0012g0084 a0002c0007t0004g0346 |
3 | HG02451.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-20-2163G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592480 | |||||||
chr11:44592607 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-20-2036G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592607 | |||||||
chr11:44592908 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0331 others(69): Show |
74 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-20-1735G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44592908 | |||||||
chr11:44593033 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0045 others(212): Show |
216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.-20-1610T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593033 | |||||||
chr11:44593259 | G | A | 7 | a0001c0001t0004g0038 a0001c0001t0004g0322 a0001c0010t0008g0247 others(4): Show |
7 | HG02818.hp2 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20-1384G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593259 | |||||||
chr11:44593343 | G | A | 2 | a0001c0001t0027g0321 a0001c0010t0004g0188 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-20-1300G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593343 | |||||||
chr11:44593354 | C | A | 1 | a0002c0002t0001g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-20-1289C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593354 | |||||||
chr11:44593357 | C | G | 2 | a0001c0016t0017g0031 a0001c0016t0048g0032 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-20-1286C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593357 | |||||||
chr11:44593363 | C | T | 1 | a0001c0016t0048g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-1280C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593363 | |||||||
chr11:44593546 | C | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0002g0172 others(58): Show |
63 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.-20-1097C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593546 | |||||||
chr11:44593547 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(224): Show |
229 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-20-1096A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593547 | |||||||
chr11:44593628 | G | A | 33 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0286 others(30): Show |
33 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.-20-1015G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593628 | |||||||
chr11:44593639 | G | GAA | 19 | a0001c0001t0001g0034 a0001c0001t0005g0213 a0001c0001t0006g0214 others(16): Show |
19 | HG00621.hp2 HG00639.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-20-1001_-20-1000d others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44593639 | ||||||
chr11:44593718 | T | G | 4 | a0002c0002t0002g0137 a0002c0002t0032g0138 a0002c0008t0001g0024 others(1): Show |
4 | NA18939.hp2 NA18967.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-925T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593718 | |||||||
chr11:44593742 | G | C | 35 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0286 others(32): Show |
35 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-20-901G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593742 | |||||||
chr11:44593880 | G | A | 82 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0059 others(79): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-20-763G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593880 | |||||||
chr11:44593977 | A | T | 349 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(346): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-20-666A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44593977 | |||||||
chr11:44593994 | TAC | T | 20 | a0001c0001t0001g0034 a0001c0001t0005g0213 a0001c0001t0006g0214 others(17): Show |
20 | HG00621.hp2 HG00639.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-20-628_-20-627del others(2): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44593994 | ||||||
chr11:44593994 | TACAC | T | 328 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(325): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.-20-630_-20-627del others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44593994 | ||||||
chr11:44594009 | A | G | 2 | a0001c0001t0004g0038 a0001c0001t0007g0326 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-20-634A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594009 | |||||||
chr11:44594149 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0249 others(93): Show |
98 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-20-494C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594149 | |||||||
chr11:44594159 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0045 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.-20-484A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594159 | |||||||
chr11:44594265 | G | T | 41 | a0001c0001t0001g0065 a0001c0001t0001g0241 a0001c0001t0001g0242 others(38): Show |
41 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20-378G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594265 | |||||||
chr11:44594295 | C | A | 1 | a0002c0003t0029g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-20-348C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594295 | |||||||
chr11:44594303 | C | G | 2 | a0001c0005t0002g0290 a0001c0005t0002g0291 |
2 | NA18939.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-20-340C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594303 | |||||||
chr11:44594388 | A | ACCAGCC | 111 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0059 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-20-232_-20-227dup others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44594388 | ||||||
chr11:44594388 | A | ACCAGCCC others(5): Show |
2 | a0001c0016t0004g0350 a0002c0025t0004g0348 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-20-238_-20-227dup others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 44594388 | ||||||
chr11:44594490 | T | A | 34 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0286 others(31): Show |
34 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.-20-153T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 2/9 | chr11 | 44594490 | |||||||
chr11:44594775 | C | T | 1 | a0002c0003t0001g0093 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.63+50C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594775 | |||||||
chr11:44594813 | G | A | 1 | a0002c0003t0044g0267 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+88G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594813 | |||||||
chr11:44594859 | A | C | 2 | a0001c0001t0001g0318 a0002c0003t0003g0319 |
2 | HG01074.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.63+134A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594859 | |||||||
chr11:44594984 | C | T | 85 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0059 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.63+259C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594984 | |||||||
chr11:44594992 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0249 others(102): Show |
107 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.63+267A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44594992 | |||||||
chr11:44595070 | C | A | 2 | a0001c0001t0004g0038 a0001c0001t0007g0326 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.63+345C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595070 | |||||||
chr11:44595091 | C | A | 1 | a0002c0002t0001g0071 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.63+366C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595091 | |||||||
chr11:44595108 | G | A | 3 | a0002c0007t0002g0128 a0002c0007t0002g0131 a0002c0007t0002g0132 |
3 | HG01167.hp2 HG01169.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.63+383G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595108 | |||||||
chr11:44595118 | G | A | 1 | a0002c0004t0001g0057 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.63+393G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595118 | |||||||
chr11:44595242 | C | T | 1 | a0001c0005t0004g0105 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.63+517C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595242 | |||||||
chr11:44595279 | G | A | 329 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(326): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.63+554G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595279 | |||||||
chr11:44595362 | C | T | 2 | a0001c0012t0004g0256 a0001c0012t0004g0257 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.63+637C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595362 | |||||||
chr11:44595489 | TA | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(222): Show |
227 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.63+766delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595489 | ||||||
chr11:44595523 | C | T | 30 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0286 others(27): Show |
30 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.63+798C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595523 | |||||||
chr11:44595530 | A | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(306): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.63+805A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595530 | |||||||
chr11:44595562 | G | A | 22 | a0001c0001t0001g0034 a0001c0001t0001g0140 a0001c0001t0005g0213 others(19): Show |
22 | HG00621.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.63+837G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595562 | |||||||
chr11:44595592 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0140 others(97): Show |
100 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.63+867G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44595592 | |||||||
chr11:44595908 | C | CA | 73 | a0001c0001t0001g0045 a0001c0001t0001g0065 a0001c0001t0001g0249 others(70): Show |
73 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.63+1206dupA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | ||||||
chr11:44595908 | C | CAA | 23 | a0001c0001t0001g0034 a0001c0001t0005g0213 a0001c0001t0013g0072 others(20): Show |
23 | HG00639.hp1 HG01106.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.63+1205_63+1206dup others(2): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | ||||||
chr11:44595908 | C | CAAAAA | 8 | a0001c0001t0001g0314 a0001c0006t0003g0343 a0001c0016t0017g0031 others(5): Show |
8 | HG00639.hp2 HG00741.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+1202_63+1206dup others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | ||||||
chr11:44595908 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0002g0316 a0001c0001t0004g0280 a0001c0001t0004g0320 |
3 | HG02572.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+1197_63+1206dup others(10): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | ||||||
chr11:44595908 | CAAAAA | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0005t0001g0088 others(47): Show |
52 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.63+1202_63+1206del others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44595908 | ||||||
chr11:44596014 | T | G | 46 | a0001c0001t0001g0034 a0001c0001t0002g0172 a0001c0001t0008g0265 others(43): Show |
46 | HG00639.hp1 HG00673.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.63+1289T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596014 | |||||||
chr11:44596118 | C | T | 1 | a0002c0007t0002g0115 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.63+1393C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596118 | |||||||
chr11:44596199 | G | A | 91 | a0001c0001t0001g0153 a0001c0001t0001g0241 a0001c0001t0001g0242 others(88): Show |
91 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.63+1474G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596199 | |||||||
chr11:44596377 | G | A | 1 | a0002c0003t0005g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.63+1652G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596377 | |||||||
chr11:44596453 | A | T | 2 | a0001c0001t0002g0172 a0001c0001t0002g0200 |
2 | NA18962.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.63+1728A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596453 | |||||||
chr11:44596619 | G | A | 2 | a0001c0009t0001g0087 a0002c0003t0014g0327 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.63+1894G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596619 | |||||||
chr11:44596641 | C | T | 6 | a0001c0010t0004g0095 a0001c0010t0007g0097 a0002c0003t0002g0323 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+1916C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596641 | |||||||
chr11:44596685 | G | C | 131 | a0001c0001t0001g0140 a0001c0001t0001g0318 a0001c0001t0002g0157 others(128): Show |
132 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.63+1960G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596685 | |||||||
chr11:44596685 | G | T | 3 | a0001c0009t0004g0085 a0002c0003t0004g0270 a0002c0015t0007g0079 |
3 | HG02630.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.63+1960G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596685 | |||||||
chr11:44596800 | G | A | 1 | a0002c0003t0003g0295 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.63+2075G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596800 | |||||||
chr11:44596816 | C | T | 1 | a0002c0002t0001g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.63+2091C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596816 | |||||||
chr11:44596935 | G | A | 3 | a0002c0003t0001g0005 a0002c0003t0001g0288 a0002c0003t0003g0005 |
3 | HG01168.hp1 HG01169.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.63+2210G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596935 | |||||||
chr11:44596951 | T | A | 1 | a0001c0001t0001g0355 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.63+2226T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44596951 | |||||||
chr11:44597148 | G | A | 6 | a0001c0010t0004g0095 a0001c0010t0007g0097 a0002c0003t0002g0323 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2423G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597148 | |||||||
chr11:44597169 | G | A | 10 | a0001c0001t0002g0157 a0001c0001t0004g0176 a0001c0001t0004g0177 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+2444G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597169 | |||||||
chr11:44597213 | T | C | 266 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0140 others(263): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.63+2488T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597213 | |||||||
chr11:44597214 | G | A | 1 | a0001c0001t0008g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+2489G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597214 | |||||||
chr11:44597232 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.63+2507C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597232 | |||||||
chr11:44597361 | TG | T | 120 | a0001c0001t0001g0140 a0001c0001t0001g0318 a0001c0001t0002g0157 others(117): Show |
121 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.63+2641delG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44597361 | ||||||
chr11:44597397 | C | G | 1 | a0001c0005t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+2672C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597397 | |||||||
chr11:44597490 | G | A | 99 | a0001c0001t0001g0153 a0001c0001t0001g0241 a0001c0001t0001g0242 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.64-2668G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597490 | |||||||
chr11:44597702 | T | C | 1 | a0001c0009t0011g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-2456T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597702 | |||||||
chr11:44597727 | T | C | 137 | a0001c0001t0001g0140 a0001c0001t0001g0249 a0001c0001t0001g0250 others(134): Show |
138 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.64-2431T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597727 | |||||||
chr11:44597733 | G | A | 5 | a0001c0001t0001g0331 a0001c0001t0008g0271 a0001c0001t0008g0329 others(2): Show |
5 | HG03041.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-2425G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597733 | |||||||
chr11:44597809 | C | A | 8 | a0001c0005t0001g0088 a0001c0005t0002g0080 a0001c0005t0037g0083 others(5): Show |
8 | NA18942.hp1 NA18948.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-2349C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44597809 | |||||||
chr11:44598142 | G | A | 1 | a0001c0001t0011g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64-2016G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598142 | |||||||
chr11:44598400 | A | ATTTT | 33 | a0001c0001t0001g0241 a0001c0001t0001g0331 a0001c0001t0002g0172 others(30): Show |
33 | HG00140.hp2 HG00408.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-1732_64-1729dup others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTT | 42 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0001t0001g0242 others(39): Show |
42 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.64-1733_64-1729dup others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTTT | 40 | a0001c0001t0001g0065 a0001c0001t0001g0250 a0001c0001t0002g0123 others(37): Show |
40 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.64-1734_64-1729dup others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTTTT | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.64-1735_64-1729dup others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTTTT others(1): Show |
29 | a0001c0001t0001g0048 a0001c0001t0001g0228 a0001c0001t0001g0286 others(26): Show |
30 | HG00423.hp2 HG00642.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1736_64-1729dup others(8): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTTTT others(2): Show |
14 | a0001c0001t0001g0307 a0001c0001t0002g0354 a0001c0001t0003g0018 others(11): Show |
14 | HG00673.hp1 HG00735.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-1737_64-1729dup others(9): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTTTT others(3): Show |
5 | a0001c0001t0003g0106 a0001c0009t0001g0033 a0002c0003t0002g0324 others(2): Show |
5 | HG00099.hp1 HG01109.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-1738_64-1729dup others(10): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTTTT others(4): Show |
3 | a0001c0010t0007g0097 a0002c0003t0014g0327 a0002c0003t0028g0261 |
3 | HG01884.hp2 HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.64-1739_64-1729dup others(11): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTTTT others(5): Show |
1 | a0001c0009t0011g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-1740_64-1729dup others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTTTT others(6): Show |
1 | a0001c0010t0004g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-1741_64-1729dup others(13): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | A | ATTTTTTT others(12): Show |
1 | a0001c0009t0001g0087 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-1747_64-1729dup others(19): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | ATT | A | 11 | a0001c0005t0001g0264 a0001c0011t0001g0333 a0001c0011t0001g0335 others(8): Show |
11 | HG03041.hp1 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-1730_64-1729del others(2): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | ATTT | A | 15 | a0001c0001t0005g0213 a0001c0001t0006g0214 a0001c0001t0013g0025 others(12): Show |
15 | HG00621.hp2 HG00741.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-1731_64-1729del others(3): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | ATTTT | A | 55 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(52): Show |
55 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.64-1732_64-1729del others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | ATTTTT | A | 5 | a0001c0001t0004g0176 a0001c0005t0002g0080 a0001c0005t0002g0290 others(2): Show |
6 | HG01515.hp2 HG01517.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1733_64-1729del others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | ATTTTTTT others(5): Show |
A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(11): Show |
20 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-1740_64-1729del others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0004g0253 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1741_64-1729del others(13): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598400 | ATTTTTTT others(8): Show |
A | 1 | a0002c0003t0007g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64-1743_64-1729del others(15): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 44598400 | ||||||
chr11:44598449 | G | C | 30 | a0001c0001t0001g0318 a0001c0001t0002g0316 a0001c0001t0003g0110 others(27): Show |
30 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1709G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598449 | |||||||
chr11:44598496 | G | A | 9 | a0001c0001t0002g0316 a0001c0001t0003g0110 a0001c0001t0004g0269 others(6): Show |
9 | HG01109.hp2 HG01168.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-1662G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598496 | |||||||
chr11:44598553 | C | T | 2 | a0001c0001t0002g0266 a0001c0001t0006g0011 |
3 | HG00099.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.64-1605C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598553 | |||||||
chr11:44598657 | G | A | 1 | a0001c0005t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-1501G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598657 | |||||||
chr11:44598706 | C | T | 26 | a0001c0001t0004g0322 a0001c0001t0004g0332 a0001c0001t0008g0265 others(23): Show |
26 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.64-1452C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598706 | |||||||
chr11:44598775 | C | T | 1 | a0001c0001t0012g0341 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-1383C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598775 | |||||||
chr11:44598792 | C | T | 1 | a0002c0003t0006g0216 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.64-1366C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598792 | |||||||
chr11:44598793 | G | A | 7 | a0001c0010t0004g0095 a0001c0010t0004g0188 a0001c0010t0007g0097 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1365G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598793 | |||||||
chr11:44598852 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0059 others(5): Show |
9 | HG00741.hp1 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1306G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598852 | |||||||
chr11:44598889 | G | A | 1 | a0001c0005t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-1269G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598889 | |||||||
chr11:44598992 | C | A | 1 | a0002c0003t0006g0139 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64-1166C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44598992 | |||||||
chr11:44599069 | G | A | 7 | a0001c0010t0004g0095 a0001c0010t0004g0188 a0001c0010t0007g0097 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1089G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599069 | |||||||
chr11:44599407 | G | A | 99 | a0001c0001t0001g0153 a0001c0001t0001g0241 a0001c0001t0001g0242 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.64-751G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599407 | |||||||
chr11:44599565 | G | A | 1 | a0001c0010t0001g0122 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.64-593G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599565 | |||||||
chr11:44599567 | C | A | 1 | a0001c0009t0001g0087 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-591C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599567 | |||||||
chr11:44599592 | G | C | 1 | a0002c0025t0004g0348 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-566G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599592 | |||||||
chr11:44599622 | G | A | 87 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(84): Show |
88 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.64-536G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599622 | |||||||
chr11:44599646 | A | G | 1 | a0002c0003t0014g0327 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.64-512A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599646 | |||||||
chr11:44599732 | C | T | 2 | a0002c0002t0001g0232 a0002c0002t0022g0272 |
2 | HG00323.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.64-426C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44599732 | |||||||
chr11:44600114 | T | C | 4 | a0002c0003t0029g0274 a0002c0003t0043g0275 a0002c0003t0045g0066 others(1): Show |
4 | HG01243.hp1 HG01496.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-44T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 3/9 | chr11 | 44600114 | |||||||
chr11:44600357 | G | T | 1 | a0001c0001t0002g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.136+127G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600357 | |||||||
chr11:44600495 | T | C | 2 | a0002c0003t0041g0311 a0002c0003t0042g0310 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.136+265T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600495 | |||||||
chr11:44600607 | G | A | 62 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(59): Show |
63 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.136+377G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600607 | |||||||
chr11:44600676 | C | G | 88 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(85): Show |
89 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.136+446C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600676 | |||||||
chr11:44600762 | G | A | 53 | a0001c0001t0001g0140 a0001c0001t0003g0175 a0001c0005t0001g0088 others(50): Show |
54 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.136+532G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600762 | |||||||
chr11:44600859 | C | T | 1 | a0002c0003t0011g0325 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136+629C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600859 | |||||||
chr11:44600898 | GACTCGA | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0052 |
3 | HG01256.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.136+673_136+678del others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 44600898 | ||||||
chr11:44600994 | G | T | 1 | a0002c0002t0001g0046 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.136+764G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44600994 | |||||||
chr11:44601031 | C | T | 1 | a0002c0003t0014g0258 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.136+801C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601031 | |||||||
chr11:44601032 | G | A | 6 | a0001c0005t0001g0088 a0001c0005t0002g0080 a0001c0005t0037g0083 others(3): Show |
6 | NA18942.hp1 NA18948.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+802G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601032 | |||||||
chr11:44601039 | C | T | 8 | a0001c0001t0001g0140 a0001c0005t0001g0203 a0001c0005t0002g0189 others(5): Show |
8 | HG00673.hp2 HG02083.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+809C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601039 | |||||||
chr11:44601161 | T | C | 258 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0140 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.136+931T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601161 | |||||||
chr11:44601179 | C | T | 62 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(59): Show |
63 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.136+949C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601179 | |||||||
chr11:44601183 | G | A | 28 | a0001c0001t0001g0318 a0001c0001t0002g0316 a0001c0001t0003g0110 others(25): Show |
28 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.136+953G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601183 | |||||||
chr11:44601489 | C | G | 9 | a0001c0001t0004g0322 a0001c0012t0016g0312 a0002c0003t0002g0039 others(6): Show |
9 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+1259C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601489 | |||||||
chr11:44601585 | C | T | 8 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0355 others(5): Show |
8 | HG00558.hp1 HG00558.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+1355C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601585 | |||||||
chr11:44601637 | C | T | 1 | a0001c0001t0007g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.136+1407C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601637 | |||||||
chr11:44601707 | T | G | 1 | a0001c0001t0051g0222 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136+1477T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601707 | |||||||
chr11:44601750 | G | A | 31 | a0001c0001t0001g0318 a0001c0001t0002g0316 a0001c0001t0003g0110 others(28): Show |
31 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.136+1520G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601750 | |||||||
chr11:44601780 | G | A | 7 | a0001c0010t0004g0095 a0001c0010t0004g0188 a0001c0010t0007g0097 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+1550G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601780 | |||||||
chr11:44601963 | C | T | 2 | a0001c0001t0002g0157 a0002c0003t0044g0267 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.136+1733C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44601963 | |||||||
chr11:44602029 | T | A | 1 | a0001c0001t0004g0332 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.136+1799T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602029 | |||||||
chr11:44602108 | G | T | 52 | a0001c0001t0001g0140 a0001c0001t0003g0175 a0001c0005t0001g0088 others(49): Show |
53 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.136+1878G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602108 | |||||||
chr11:44602122 | T | C | 88 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(85): Show |
89 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.136+1892T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602122 | |||||||
chr11:44602145 | C | T | 1 | a0002c0019t0011g0344 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136+1915C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602145 | |||||||
chr11:44602270 | G | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0003g0098 others(6): Show |
9 | HG00642.hp1 HG01192.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+2040G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602270 | |||||||
chr11:44602347 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(41): Show |
45 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+2117G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602347 | |||||||
chr11:44602599 | T | C | 14 | a0001c0001t0005g0213 a0001c0001t0006g0214 a0001c0001t0013g0025 others(11): Show |
14 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.136+2369T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602599 | |||||||
chr11:44602605 | A | G | 1 | a0001c0009t0004g0238 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.136+2375A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602605 | |||||||
chr11:44602627 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.136+2397G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602627 | |||||||
chr11:44602630 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.136+2400C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602630 | |||||||
chr11:44602672 | GA | G | 62 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(59): Show |
63 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.137-2377delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 44602672 | ||||||
chr11:44602681 | A | T | 89 | a0001c0001t0001g0065 a0001c0001t0001g0249 a0001c0001t0001g0250 others(86): Show |
89 | HG00140.hp2 HG00621.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.137-2377A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602681 | |||||||
chr11:44602734 | C | T | 1 | a0002c0003t0001g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.137-2324C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602734 | |||||||
chr11:44602891 | C | T | 1 | a0001c0012t0016g0312 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.137-2167C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602891 | |||||||
chr11:44602901 | C | G | 89 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(86): Show |
90 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.137-2157C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602901 | |||||||
chr11:44602901 | C | T | 1 | a0001c0010t0001g0122 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.137-2157C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602901 | |||||||
chr11:44602930 | C | T | 31 | a0001c0001t0001g0318 a0001c0001t0002g0316 a0001c0001t0003g0110 others(28): Show |
31 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-2128C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602930 | |||||||
chr11:44602960 | G | A | 31 | a0001c0001t0001g0318 a0001c0001t0002g0316 a0001c0001t0003g0110 others(28): Show |
31 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-2098G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44602960 | |||||||
chr11:44603255 | T | C | 89 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(86): Show |
90 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.137-1803T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603255 | |||||||
chr11:44603264 | G | A | 1 | a0002c0002t0001g0035 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.137-1794G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603264 | |||||||
chr11:44603373 | C | G | 1 | a0001c0005t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.137-1685C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603373 | |||||||
chr11:44603408 | C | T | 4 | a0001c0016t0004g0350 a0001c0016t0017g0031 a0001c0016t0048g0032 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-1650C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603408 | |||||||
chr11:44603449 | C | G | 1 | a0002c0008t0004g0090 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.137-1609C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603449 | |||||||
chr11:44603516 | G | A | 2 | a0001c0009t0001g0087 a0002c0003t0014g0327 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.137-1542G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603516 | |||||||
chr11:44603551 | C | T | 2 | a0002c0003t0002g0039 a0002c0003t0011g0260 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.137-1507C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603551 | |||||||
chr11:44603592 | C | T | 1 | a0001c0005t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.137-1466C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603592 | |||||||
chr11:44603629 | C | T | 5 | a0001c0001t0001g0065 a0001c0001t0008g0197 a0002c0003t0001g0093 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-1429C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603629 | |||||||
chr11:44603632 | G | A | 1 | a0001c0016t0004g0350 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137-1426G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603632 | |||||||
chr11:44603762 | T | C | 1 | a0001c0001t0004g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.137-1296T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603762 | |||||||
chr11:44603792 | T | A | 1 | a0002c0008t0002g0111 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.137-1266T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603792 | |||||||
chr11:44603799 | G | A | 1 | a0002c0002t0002g0150 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.137-1259G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603799 | |||||||
chr11:44603810 | G | A | 17 | a0001c0001t0004g0322 a0001c0001t0008g0265 a0001c0010t0004g0095 others(14): Show |
17 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.137-1248G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603810 | |||||||
chr11:44603842 | T | C | 90 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(87): Show |
91 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.137-1216T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603842 | |||||||
chr11:44603898 | C | T | 2 | a0001c0001t0051g0222 a0002c0003t0004g0345 |
2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.137-1160C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603898 | |||||||
chr11:44603899 | G | A | 1 | a0002c0004t0003g0202 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.137-1159G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603899 | |||||||
chr11:44603943 | T | C | 91 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(88): Show |
92 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.137-1115T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603943 | |||||||
chr11:44603961 | C | A | 3 | a0002c0002t0001g0232 a0002c0002t0003g0053 a0002c0002t0022g0272 |
3 | HG00323.hp2 HG02055.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.137-1097C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44603961 | |||||||
chr11:44604062 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.137-996C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604062 | |||||||
chr11:44604065 | C | T | 1 | a0001c0006t0001g0164 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.137-993C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604065 | |||||||
chr11:44604321 | C | T | 3 | a0001c0009t0015g0223 a0001c0012t0004g0256 a0001c0012t0004g0257 |
3 | HG02451.hp1 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.137-737C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604321 | |||||||
chr11:44604350 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0043 a0002c0002t0001g0046 others(1): Show |
4 | HG01255.hp1 HG01928.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-708G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604350 | |||||||
chr11:44604430 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0003g0008 a0001c0001t0046g0094 |
3 | HG02970.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.137-628G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604430 | |||||||
chr11:44604529 | GTTA | G | 10 | a0001c0011t0001g0333 a0001c0011t0001g0335 a0001c0011t0001g0336 others(7): Show |
10 | NA18942.hp2 NA18950.hp2 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-524_137-522del others(3): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 44604529 | ||||||
chr11:44604706 | C | T | 1 | a0001c0001t0002g0316 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.137-352C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604706 | |||||||
chr11:44604732 | TTGG | T | 10 | a0001c0011t0001g0333 a0001c0011t0001g0335 a0001c0011t0001g0336 others(7): Show |
10 | NA18942.hp2 NA18950.hp2 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-322_137-320del others(3): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 44604732 | ||||||
chr11:44604826 | G | A | 1 | a0001c0016t0004g0350 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137-232G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604826 | |||||||
chr11:44604834 | G | A | 1 | a0001c0009t0011g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137-224G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604834 | |||||||
chr11:44604847 | G | A | 98 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0249 others(95): Show |
99 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.137-211G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604847 | |||||||
chr11:44604911 | C | G | 99 | a0001c0001t0001g0153 a0001c0001t0001g0241 a0001c0001t0001g0242 others(96): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.137-147C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604911 | |||||||
chr11:44604930 | C | A | 7 | a0001c0006t0003g0192 a0001c0006t0003g0343 a0001c0006t0005g0273 others(4): Show |
7 | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-128C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44604930 | |||||||
chr11:44605043 | T | A | 3 | a0002c0003t0001g0005 a0002c0003t0001g0288 a0002c0003t0003g0005 |
3 | HG01168.hp1 HG01169.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.137-15T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 4/9 | chr11 | 44605043 | |||||||
chr11:44605562 | G | A | 1 | a0002c0007t0002g0115 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.336+133G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605562 | |||||||
chr11:44605618 | G | A | 88 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(85): Show |
89 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.336+189G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605618 | |||||||
chr11:44605720 | T | C | 1 | a0001c0009t0011g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.336+291T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605720 | |||||||
chr11:44605842 | A | G | 63 | a0001c0001t0001g0140 a0001c0001t0002g0157 a0001c0001t0003g0175 others(60): Show |
64 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.336+413A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605842 | |||||||
chr11:44605857 | C | T | 1 | a0002c0008t0002g0111 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.336+428C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44605857 | |||||||
chr11:44606162 | T | G | 87 | a0001c0001t0002g0157 a0001c0001t0003g0175 a0001c0001t0004g0176 others(84): Show |
88 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.336+733T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606162 | |||||||
chr11:44606234 | G | A | 1 | a0001c0005t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.336+805G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606234 | |||||||
chr11:44606298 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.336+869G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606298 | |||||||
chr11:44606467 | C | CA | 187 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0140 others(184): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.336+1058dupA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44606467 | ||||||
chr11:44606467 | C | CAA | 78 | a0001c0001t0002g0157 a0001c0001t0002g0316 a0001c0001t0003g0175 others(75): Show |
79 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.336+1057_336+1058d others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44606467 | ||||||
chr11:44606467 | C | CAAA | 15 | a0001c0001t0013g0072 a0001c0005t0002g0290 a0001c0009t0011g0263 others(12): Show |
15 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.336+1056_336+1058d others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44606467 | ||||||
chr11:44606543 | A | G | 1 | a0002c0007t0003g0330 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.336+1114A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606543 | |||||||
chr11:44606680 | G | T | 1 | a0001c0001t0003g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.336+1251G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606680 | |||||||
chr11:44606817 | A | G | 6 | a0001c0001t0001g0065 a0001c0001t0008g0197 a0002c0003t0001g0093 others(3): Show |
6 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.336+1388A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606817 | |||||||
chr11:44606852 | C | T | 13 | a0001c0001t0004g0322 a0001c0001t0008g0265 a0001c0009t0015g0223 others(10): Show |
13 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+1423C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606852 | |||||||
chr11:44606871 | C | T | 1 | a0002c0003t0038g0278 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.336+1442C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606871 | |||||||
chr11:44606917 | C | T | 1 | a0002c0003t0003g0295 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.336+1488C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606917 | |||||||
chr11:44606929 | C | T | 137 | a0001c0001t0001g0140 a0001c0001t0001g0249 a0001c0001t0001g0250 others(134): Show |
138 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.336+1500C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44606929 | |||||||
chr11:44607525 | C | G | 11 | a0001c0001t0013g0072 a0001c0011t0001g0333 a0001c0011t0001g0335 others(8): Show |
11 | HG01255.hp2 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.336+2096C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44607525 | |||||||
chr11:44607681 | T | C | 1 | a0002c0003t0003g0295 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.336+2252T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44607681 | |||||||
chr11:44607793 | T | C | 1 | a0001c0005t0004g0105 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.336+2364T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44607793 | |||||||
chr11:44607914 | G | A | 86 | a0001c0001t0002g0157 a0001c0001t0003g0175 a0001c0001t0004g0176 others(83): Show |
87 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.336+2485G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44607914 | |||||||
chr11:44608084 | C | T | 1 | a0002c0002t0003g0168 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.336+2655C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608084 | |||||||
chr11:44608252 | G | A | 5 | a0001c0001t0001g0331 a0001c0001t0008g0271 a0001c0001t0008g0329 others(2): Show |
5 | HG03041.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+2823G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608252 | |||||||
chr11:44608303 | C | T | 7 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0355 others(4): Show |
7 | HG00558.hp1 HG00558.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.336+2874C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608303 | |||||||
chr11:44608361 | G | A | 1 | a0002c0008t0001g0024 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.336+2932G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608361 | |||||||
chr11:44608405 | C | T | 1 | a0002c0015t0003g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.336+2976C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608405 | |||||||
chr11:44608434 | C | A | 1 | a0002c0002t0002g0196 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.336+3005C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608434 | |||||||
chr11:44608499 | A | G | 257 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0140 others(254): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.336+3070A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608499 | |||||||
chr11:44608509 | A | G | 87 | a0001c0001t0002g0157 a0001c0001t0003g0175 a0001c0001t0004g0176 others(84): Show |
88 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.336+3080A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608509 | |||||||
chr11:44608515 | T | C | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0004g0248 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.336+3086T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608515 | |||||||
chr11:44608642 | A | G | 36 | a0001c0005t0001g0088 a0001c0005t0001g0203 a0001c0005t0001g0204 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.336+3213A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608642 | |||||||
chr11:44608755 | A | G | 246 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0153 others(243): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.336+3326A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608755 | |||||||
chr11:44608770 | A | G | 3 | a0001c0009t0015g0223 a0001c0012t0004g0256 a0001c0012t0004g0257 |
3 | HG02451.hp1 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.336+3341A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608770 | |||||||
chr11:44608847 | C | A | 1 | a0002c0003t0001g0012 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.336+3418C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608847 | |||||||
chr11:44608854 | C | T | 13 | a0001c0001t0013g0072 a0001c0009t0001g0087 a0001c0011t0001g0333 others(10): Show |
13 | HG01255.hp2 HG01884.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+3425C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608854 | |||||||
chr11:44608860 | G | A | 5 | a0001c0001t0001g0331 a0001c0001t0008g0271 a0001c0001t0008g0329 others(2): Show |
5 | HG03041.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+3431G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608860 | |||||||
chr11:44608913 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.336+3484C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608913 | |||||||
chr11:44608914 | G | T | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0004g0248 others(2): Show |
5 | HG02486.hp2 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.336+3485G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44608914 | |||||||
chr11:44609003 | A | G | 11 | a0001c0001t0013g0072 a0001c0011t0001g0333 a0001c0011t0001g0335 others(8): Show |
11 | HG01255.hp2 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.336+3574A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609003 | |||||||
chr11:44609095 | C | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0043 a0002c0002t0001g0046 others(1): Show |
4 | HG01255.hp1 HG01928.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.336+3666C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609095 | |||||||
chr11:44609120 | T | C | 1 | a0001c0001t0013g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.336+3691T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609120 | |||||||
chr11:44609129 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0003g0008 |
2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.336+3700C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609129 | |||||||
chr11:44609137 | G | A | 9 | a0001c0001t0004g0322 a0001c0012t0016g0312 a0002c0003t0002g0039 others(6): Show |
9 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.336+3708G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609137 | |||||||
chr11:44609191 | C | T | 3 | a0002c0003t0001g0005 a0002c0003t0001g0288 a0002c0003t0003g0005 |
3 | HG01168.hp1 HG01169.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.336+3762C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609191 | |||||||
chr11:44609535 | C | A | 2 | a0002c0004t0009g0063 a0002c0004t0019g0058 |
2 | HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.336+4106C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609535 | |||||||
chr11:44609652 | G | A | 118 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0318 others(115): Show |
119 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.336+4223G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609652 | |||||||
chr11:44609809 | G | A | 1 | a0002c0003t0001g0217 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.336+4380G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609809 | |||||||
chr11:44609983 | G | A | 1 | a0002c0025t0004g0348 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.336+4554G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609983 | |||||||
chr11:44609995 | G | A | 1 | a0001c0001t0008g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.336+4566G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44609995 | |||||||
chr11:44610105 | T | C | 142 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0249 others(139): Show |
143 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.336+4676T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610105 | |||||||
chr11:44610295 | A | G | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(349): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.336+4866A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610295 | |||||||
chr11:44610319 | T | C | 1 | a0001c0009t0011g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.336+4890T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610319 | |||||||
chr11:44610415 | G | A | 7 | a0001c0010t0004g0095 a0001c0010t0004g0188 a0001c0010t0007g0097 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-4857G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610415 | |||||||
chr11:44610611 | C | T | 4 | a0001c0001t0001g0065 a0001c0001t0008g0197 a0002c0003t0001g0093 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-4661C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610611 | |||||||
chr11:44610635 | G | C | 1 | a0002c0003t0001g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.337-4637G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610635 | |||||||
chr11:44610792 | C | T | 4 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0004g0248 others(1): Show |
4 | HG02486.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-4480C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610792 | |||||||
chr11:44610831 | C | CT | 7 | a0001c0001t0001g0065 a0001c0001t0008g0197 a0001c0009t0011g0263 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-4431dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44610831 | ||||||
chr11:44610904 | G | A | 1 | a0001c0001t0002g0200 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.337-4368G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44610904 | |||||||
chr11:44611055 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.337-4217G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611055 | |||||||
chr11:44611301 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0003g0008 a0001c0001t0004g0038 others(5): Show |
8 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-3971G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611301 | |||||||
chr11:44611348 | C | T | 52 | a0001c0001t0003g0175 a0001c0005t0001g0088 a0001c0005t0001g0203 others(49): Show |
53 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.337-3924C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611348 | |||||||
chr11:44611404 | T | C | 103 | a0001c0001t0001g0153 a0001c0001t0001g0241 a0001c0001t0001g0242 others(100): Show |
103 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.337-3868T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611404 | |||||||
chr11:44611510 | G | A | 33 | a0001c0001t0001g0140 a0001c0001t0001g0318 a0001c0001t0002g0157 others(30): Show |
33 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.337-3762G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611510 | |||||||
chr11:44611518 | C | T | 33 | a0001c0001t0001g0140 a0001c0001t0001g0318 a0001c0001t0002g0157 others(30): Show |
33 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.337-3754C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611518 | |||||||
chr11:44611618 | C | T | 46 | a0001c0001t0001g0140 a0001c0001t0001g0249 a0001c0001t0001g0250 others(43): Show |
46 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.337-3654C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611618 | |||||||
chr11:44611636 | A | G | 1 | a0001c0009t0011g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.337-3636A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611636 | |||||||
chr11:44611842 | ATGGAAAC others(12): Show |
A | 24 | a0001c0001t0005g0213 a0001c0001t0006g0214 a0001c0001t0013g0025 others(21): Show |
24 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.337-3416_337-3398d others(21): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44611842 | ||||||
chr11:44611845 | G | C | 2 | a0001c0001t0008g0271 a0001c0001t0008g0329 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-3427G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611845 | |||||||
chr11:44611881 | A | G | 1 | a0002c0002t0001g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.337-3391A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44611881 | |||||||
chr11:44612092 | G | C | 1 | a0001c0001t0008g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.337-3180G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612092 | |||||||
chr11:44612175 | C | T | 1 | a0001c0010t0004g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.337-3097C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612175 | |||||||
chr11:44612197 | G | A | 1 | a0002c0008t0002g0154 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.337-3075G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612197 | |||||||
chr11:44612510 | T | C | 2 | a0002c0004t0002g0225 a0002c0004t0002g0226 |
2 | NA18954.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.337-2762T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612510 | |||||||
chr11:44612535 | C | CT | 32 | a0001c0001t0004g0322 a0001c0001t0008g0265 a0001c0009t0004g0238 others(29): Show |
32 | HG00099.hp1 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.337-2720dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612535 | ||||||
chr11:44612535 | CT | C | 113 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0065 others(110): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.337-2720delT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612535 | ||||||
chr11:44612595 | G | A | 24 | a0001c0001t0005g0213 a0001c0001t0006g0214 a0001c0001t0013g0025 others(21): Show |
24 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.337-2677G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612595 | |||||||
chr11:44612623 | A | AT | 111 | a0001c0001t0001g0008 a0001c0001t0001g0153 a0001c0001t0001g0241 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.337-2622dupT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612623 | A | ATT | 35 | a0001c0001t0001g0065 a0001c0001t0003g0175 a0001c0001t0015g0351 others(32): Show |
35 | HG00140.hp1 HG00673.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.337-2623_337-2622d others(4): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612623 | A | ATTT | 47 | a0001c0001t0005g0213 a0001c0001t0006g0214 a0001c0001t0008g0197 others(44): Show |
48 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.337-2624_337-2622d others(5): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612623 | A | ATTTT | 18 | a0001c0001t0002g0200 a0001c0001t0003g0110 a0001c0001t0013g0025 others(15): Show |
18 | HG00621.hp2 HG00741.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.337-2625_337-2622d others(6): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612623 | A | ATTTTT | 20 | a0001c0001t0001g0140 a0001c0001t0001g0318 a0001c0001t0002g0172 others(17): Show |
20 | HG01074.hp2 HG01109.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.337-2626_337-2622d others(7): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612623 | A | ATTTTTT | 8 | a0001c0001t0002g0316 a0001c0001t0008g0265 a0001c0009t0011g0263 others(5): Show |
8 | HG00140.hp2 HG01346.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-2627_337-2622d others(8): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612623 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0250 a0001c0001t0004g0248 |
2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.337-2631_337-2622d others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612623 | A | ATTTTTTT others(4): Show |
1 | a0002c0003t0011g0260 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.337-2632_337-2622d others(13): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612623 | AT | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0052 others(8): Show |
11 | HG01168.hp1 HG01169.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.337-2622delT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612623 | ATTTTTTT others(3): Show |
A | 3 | a0001c0009t0015g0223 a0001c0012t0004g0256 a0001c0012t0004g0257 |
3 | HG02451.hp1 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.337-2631_337-2622d others(12): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44612623 | ||||||
chr11:44612779 | C | G | 1 | a0001c0009t0002g0186 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.337-2493C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612779 | |||||||
chr11:44612907 | A | G | 1 | a0001c0010t0040g0030 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.337-2365A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44612907 | |||||||
chr11:44613017 | A | G | 3 | a0001c0001t0004g0038 a0001c0001t0007g0326 a0001c0010t0008g0247 |
3 | HG02818.hp2 HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.337-2255A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613017 | |||||||
chr11:44613171 | C | T | 1 | a0002c0003t0004g0345 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.337-2101C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613171 | |||||||
chr11:44613176 | T | C | 10 | a0001c0010t0004g0095 a0001c0010t0004g0188 a0001c0010t0007g0097 others(7): Show |
10 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.337-2096T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613176 | |||||||
chr11:44613215 | T | A | 286 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0140 others(283): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.337-2057T>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613215 | |||||||
chr11:44613233 | CATTTGCC others(9): Show |
C | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-2038_337-2023d others(18): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613233 | |||||||
chr11:44613308 | G | A | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1964G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613308 | |||||||
chr11:44613324 | A | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1948A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613324 | |||||||
chr11:44613331 | C | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1941C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613331 | |||||||
chr11:44613332 | T | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1940T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613332 | |||||||
chr11:44613360 | C | T | 29 | a0001c0001t0001g0065 a0001c0001t0001g0318 a0001c0001t0002g0316 others(26): Show |
29 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.337-1912C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613360 | |||||||
chr11:44613403 | A | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1869A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613403 | |||||||
chr11:44613406 | C | A | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1866C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613406 | |||||||
chr11:44613415 | T | C | 10 | a0001c0001t0001g0008 a0001c0001t0003g0008 a0001c0001t0046g0094 others(7): Show |
10 | HG02451.hp1 HG02622.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.337-1857T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613415 | |||||||
chr11:44613445 | T | C | 34 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0318 others(31): Show |
34 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.337-1827T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613445 | |||||||
chr11:44613448 | G | A | 1 | a0002c0008t0002g0154 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.337-1824G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613448 | |||||||
chr11:44613465 | T | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1807T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613465 | |||||||
chr11:44613468 | T | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1804T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613468 | |||||||
chr11:44613469 | G | T | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1803G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613469 | |||||||
chr11:44613470 | C | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1802C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613470 | |||||||
chr11:44613471 | T | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1801T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613471 | |||||||
chr11:44613475 | C | T | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1797C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613475 | |||||||
chr11:44613477 | C | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1795C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613477 | |||||||
chr11:44613535 | G | A | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1737G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613535 | |||||||
chr11:44613536 | A | T | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1736A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613536 | |||||||
chr11:44613537 | T | C | 34 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0318 others(31): Show |
34 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.337-1735T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613537 | |||||||
chr11:44613539 | T | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1733T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613539 | |||||||
chr11:44613545 | A | T | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1727A>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613545 | |||||||
chr11:44613553 | T | C | 1 | a0002c0008t0001g0207 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.337-1719T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613553 | |||||||
chr11:44613555 | T | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1717T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613555 | |||||||
chr11:44613561 | G | T | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-1711G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613561 | |||||||
chr11:44613658 | G | A | 182 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0318 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.337-1614G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613658 | |||||||
chr11:44613695 | T | C | 1 | a0001c0001t0013g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.337-1577T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613695 | |||||||
chr11:44613715 | T | C | 17 | a0001c0001t0004g0322 a0001c0001t0008g0265 a0001c0010t0004g0095 others(14): Show |
17 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.337-1557T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613715 | |||||||
chr11:44613812 | C | T | 2 | a0001c0016t0017g0031 a0001c0016t0048g0032 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.337-1460C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44613812 | |||||||
chr11:44613843 | CA | C | 227 | a0001c0001t0001g0008 a0001c0001t0003g0008 a0001c0001t0003g0110 others(224): Show |
228 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.337-1417delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44613843 | ||||||
chr11:44613990 | GTTGTTGT others(5): Show |
G | 98 | a0001c0006t0001g0037 a0001c0006t0001g0120 a0001c0006t0001g0164 others(95): Show |
99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.337-1264_337-1253d others(14): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 44613990 | ||||||
chr11:44614010 | TG | T | 15 | a0001c0001t0003g0110 a0001c0001t0005g0213 a0001c0001t0006g0016 others(12): Show |
15 | HG00621.hp2 HG00741.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.337-1261delG | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614010 | |||||||
chr11:44614020 | T | C | 211 | a0001c0001t0001g0008 a0001c0001t0003g0008 a0001c0001t0003g0110 others(208): Show |
212 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.337-1252T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614020 | |||||||
chr11:44614076 | G | A | 9 | a0001c0001t0004g0322 a0001c0012t0016g0312 a0002c0003t0002g0039 others(6): Show |
9 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-1196G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614076 | |||||||
chr11:44614272 | G | T | 2 | a0001c0018t0012g0268 a0001c0018t0012g0340 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.337-1000G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614272 | |||||||
chr11:44614420 | A | G | 1 | a0001c0001t0004g0253 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.337-852A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614420 | |||||||
chr11:44614525 | T | G | 1 | a0002c0008t0002g0297 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.337-747T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614525 | |||||||
chr11:44614598 | A | G | 9 | a0001c0001t0004g0322 a0001c0012t0016g0312 a0002c0003t0002g0039 others(6): Show |
9 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-674A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614598 | |||||||
chr11:44614641 | G | A | 1 | a0001c0001t0006g0011 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.337-631G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614641 | |||||||
chr11:44614693 | G | A | 1 | a0002c0008t0001g0129 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.337-579G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614693 | |||||||
chr11:44614982 | G | A | 1 | a0002c0008t0002g0154 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.337-290G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614982 | |||||||
chr11:44614997 | G | A | 100 | a0001c0006t0001g0037 a0001c0006t0001g0120 a0001c0006t0001g0164 others(97): Show |
101 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.337-275G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44614997 | |||||||
chr11:44615088 | T | G | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-184T>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615088 | |||||||
chr11:44615121 | G | C | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-151G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615121 | |||||||
chr11:44615122 | C | A | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-150C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615122 | |||||||
chr11:44615123 | A | C | 1 | a0001c0006t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.337-149A>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615123 | |||||||
chr11:44615130 | G | C | 1 | a0002c0008t0004g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.337-142G>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615130 | |||||||
chr11:44615134 | G | T | 71 | a0001c0005t0001g0088 a0001c0005t0001g0203 a0001c0005t0001g0204 others(68): Show |
71 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.337-138G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615134 | |||||||
chr11:44615203 | G | A | 1 | a0001c0001t0017g0091 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.337-69G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 6/9 | chr11 | 44615203 | |||||||
chr11:44615764 | T | C | 1 | a0001c0001t0008g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.438+391T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615764 | |||||||
chr11:44615810 | T | C | 1 | a0002c0003t0045g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.438+437T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615810 | |||||||
chr11:44615834 | A | G | 10 | a0001c0001t0004g0322 a0001c0001t0008g0265 a0001c0012t0016g0312 others(7): Show |
10 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+461A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615834 | |||||||
chr11:44615890 | T | C | 15 | a0001c0011t0001g0333 a0001c0011t0001g0335 a0001c0011t0001g0336 others(12): Show |
15 | HG00673.hp2 NA18949.hp1 NA18950.hp2 others(12): Show |
intron_variant | MODIFIER | c.438+517T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615890 | |||||||
chr11:44615929 | C | T | 6 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0004g0248 others(3): Show |
6 | HG02451.hp1 HG02486.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+556C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615929 | |||||||
chr11:44615930 | A | G | 351 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(348): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.438+557A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44615930 | |||||||
chr11:44616021 | C | T | 10 | a0001c0001t0004g0322 a0001c0001t0008g0265 a0001c0012t0016g0312 others(7): Show |
10 | HG02280.hp2 HG02717.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+648C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616021 | |||||||
chr11:44616096 | C | T | 1 | a0002c0002t0003g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.438+723C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616096 | |||||||
chr11:44616507 | A | G | 1 | a0002c0004t0001g0057 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.438+1134A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616507 | |||||||
chr11:44616558 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0003g0008 a0001c0001t0004g0038 others(5): Show |
8 | HG02818.hp2 HG02896.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.438+1185C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616558 | |||||||
chr11:44616666 | G | A | 1 | a0001c0001t0004g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438+1293G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616666 | |||||||
chr11:44616849 | A | G | 3 | a0001c0001t0008g0265 a0002c0003t0002g0039 a0002c0003t0011g0260 |
3 | HG02818.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.439-1313A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616849 | |||||||
chr11:44616850 | C | T | 1 | a0002c0025t0004g0348 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.439-1312C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44616850 | |||||||
chr11:44617019 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0003g0008 a0001c0001t0046g0094 |
3 | HG02970.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.439-1143C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617019 | |||||||
chr11:44617034 | T | C | 5 | a0001c0001t0001g0318 a0002c0003t0002g0305 a0002c0003t0003g0295 others(2): Show |
5 | HG00140.hp2 HG01074.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-1128T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617034 | |||||||
chr11:44617105 | G | A | 45 | a0001c0001t0001g0065 a0001c0001t0001g0318 a0001c0001t0003g0175 others(42): Show |
45 | HG00140.hp2 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.439-1057G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617105 | |||||||
chr11:44617222 | G | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.439-940G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617222 | |||||||
chr11:44617354 | G | T | 4 | a0001c0001t0008g0265 a0002c0003t0002g0039 a0002c0003t0011g0260 others(1): Show |
4 | HG02818.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-808G>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617354 | |||||||
chr11:44617508 | A | G | 1 | a0001c0009t0015g0223 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.439-654A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617508 | |||||||
chr11:44617560 | G | GA | 14 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0286 others(11): Show |
14 | HG01952.hp1 HG02015.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.439-580dupA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 44617560 | ||||||
chr11:44617560 | GA | G | 199 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0249 others(196): Show |
200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.439-580delA | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 44617560 | ||||||
chr11:44617560 | GAA | G | 35 | a0001c0001t0003g0110 a0001c0001t0006g0016 a0001c0001t0013g0072 others(32): Show |
35 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.439-581_439-580del others(2): Show |
CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 44617560 | ||||||
chr11:44617618 | CT | C | 11 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0331 others(8): Show |
11 | HG02451.hp1 HG02486.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.439-537delT | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 44617618 | ||||||
chr11:44617635 | C | G | 21 | a0001c0001t0001g0065 a0001c0001t0001g0318 a0001c0001t0004g0269 others(18): Show |
21 | HG00140.hp2 HG01074.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.439-527C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617635 | |||||||
chr11:44617706 | C | A | 1 | a0001c0011t0001g0335 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.439-456C>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617706 | |||||||
chr11:44617836 | C | G | 2 | a0001c0001t0015g0351 a0002c0025t0004g0348 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.439-326C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44617836 | |||||||
chr11:44618001 | T | C | 65 | a0001c0001t0001g0065 a0001c0001t0001g0318 a0001c0001t0003g0175 others(62): Show |
65 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.439-161T>C | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44618001 | |||||||
chr11:44618048 | G | A | 1 | a0002c0002t0002g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.439-114G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 7/9 | chr11 | 44618048 | |||||||
chr11:44618371 | C | G | 1 | a0001c0011t0005g0317 | 1 | NA19000.hp1 | splice_region_variant&intron_variant | LOW | c.642+6C>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618371 | |||||||
chr11:44618371 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
179 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(176): Show |
splice_region_variant&intron_variant | LOW | c.642+6C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618371 | |||||||
chr11:44618382 | G | A | 81 | a0001c0001t0003g0309 a0001c0006t0001g0037 a0001c0006t0001g0120 others(78): Show |
81 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.642+17G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618382 | |||||||
chr11:44618466 | A | G | 281 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0065 others(278): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.642+101A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618466 | |||||||
chr11:44618494 | A | G | 9 | a0001c0001t0004g0308 a0001c0001t0015g0262 a0001c0009t0001g0087 others(6): Show |
9 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.642+129A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618494 | |||||||
chr11:44618550 | C | T | 28 | a0001c0001t0001g0045 a0001c0001t0001g0249 a0001c0001t0001g0250 others(25): Show |
28 | HG00621.hp2 HG00639.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.643-90C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 8/9 | chr11 | 44618550 | |||||||
chr11:44618909 | C | T | 1 | a0001c0001t0015g0262 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.727-140C>T | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/9 | chr11 | 44618909 | |||||||
chr11:44618927 | A | G | 20 | a0001c0001t0001g0045 a0001c0001t0002g0316 a0001c0001t0003g0110 others(17): Show |
20 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.727-122A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/9 | chr11 | 44618927 | |||||||
chr11:44618969 | A | G | 4 | a0001c0001t0001g0331 a0001c0001t0008g0271 a0001c0001t0008g0329 others(1): Show |
4 | HG03471.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-80A>G | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/9 | chr11 | 44618969 | |||||||
chr11:44619035 | G | A | 1 | a0001c0006t0002g0151 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.727-14G>A | CD82 | ENSG00000085117.12 | transcript | ENST00000227155.9 | protein_coding | 9/9 | chr11 | 44619035 |