Item | Value |
---|---|
geneid | 10077 |
ensemblid | ENSG00000064201.16 |
hgncid | 13410 |
symbol | TSPAN32 |
name | tetraspanin 32 |
refseq_nuc | NM_139022.3 |
refseq_prot | NP_620591.3 |
ensembl_nuc | ENST00000182290.9 |
ensembl_prot | ENSP00000182290.5 |
mane_status | MANE Select |
chr | chr11 |
start | 2302013 |
end | 2318204 |
strand | + |
ver | v1.2 |
region | chr11:2302013-2318204 |
region5000 | chr11:2297013-2323204 |
regionname0 | TSPAN32_chr11_2302013_2318204 |
regionname5000 | TSPAN32_chr11_2297013_2323204 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 320 | 386 | 93 | 75 | 159 | 13 | 44 | 109 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | MGPWS others(315): Show |
chr11 | 2297013 | 2323204 |
a0002 | 0/0 | 320 | 14 | 0 | 0 | 14 | 0 | 0 | 14 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | MGPWS others(315): Show |
chr11 | 2297013 | 2323204 |
a0003 | 0/0 | 320 | 5 | 0 | 2 | 0 | 1 | 2 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | MGPWS others(315): Show |
chr11 | 2297013 | 2323204 |
a0004 | 0/0 | 320 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | MGPWS others(315): Show |
chr11 | 2297013 | 2323204 |
a0005 | 0/0 | 320 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | MGPWS others(315): Show |
chr11 | 2297013 | 2323204 |
a0006 | 0/0 | 320 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | MGPWS others(315): Show |
chr11 | 2297013 | 2323204 |
a0007 | 0/0 | 5 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | MGPWS | chr11 | 2297013 | 2323204 |
a0008 | 0/0 | 320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | MGPWS others(315): Show |
chr11 | 2297013 | 2323204 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 960 | 212 | 41 | 30 | 125 | 2 | 13 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0001c0002 | 0/1 | 960 | 170 | 51 | 45 | 32 | 11 | 30 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0001c0007 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0001c0008 | 0/0 | 960 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0001c0010 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0001c0012 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0002c0003 | 0/0 | 960 | 14 | 0 | 0 | 14 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0003c0004 | 0/0 | 960 | 5 | 0 | 2 | 0 | 1 | 2 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0004c0005 | 0/0 | 960 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0005c0006 | 0/0 | 960 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0006c0011 | 0/0 | 960 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0007c0013 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 | ||
a0008c0009 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | ATGGG others(955): Show |
chr11 | 2297013 | 2323204 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1380 | 210 | 40 | 30 | 125 | 2 | 12 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0001c0001t0002 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0001c0001t0004 | 0/0 | 1380 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0001c0002t0001 | 0/1 | 1380 | 167 | 48 | 45 | 32 | 11 | 30 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0001c0002t0002 | 0/0 | 1380 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0001c0007t0001 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0001c0008t0001 | 0/0 | 1380 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0001c0010t0001 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0001c0012t0003 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0002c0003t0001 | 0/0 | 1380 | 14 | 0 | 0 | 14 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0003c0004t0001 | 0/0 | 1380 | 5 | 0 | 2 | 0 | 1 | 2 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0004c0005t0001 | 0/0 | 1380 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0005c0006t0001 | 0/0 | 1380 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0006c0011t0001 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0007c0013t0001 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
a0008c0009t0001 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | AGGGC others(1375): Show |
chr11 | 2297013 | 2323204 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 24 | 0 | 3 | 21 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0004 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0005 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0035 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0002 | 0/0 | 12 | 0 | 3 | 5 | 2 | 2 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0007 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0008t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0010t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0001c0012t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0002c0003t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0002c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0003c0004t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0003c0004t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0003c0004t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0003c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0004c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0004c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0005c0006t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0005c0006t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0006c0011t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0007c0013t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
a0008c0009t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0002 | t0001 | g0009 | EUR | FIN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0130 | EUR | FIN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0192 | EUR | FIN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | FIN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00741 | hp1 | a0006 | c0011 | t0001 | g0179 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01256 | hp2 | a0003 | c0004 | t0001 | g0212 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01258 | hp2 | a0003 | c0004 | t0001 | g0211 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0023 | EUR | IBS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01516 | hp1 | a0003 | c0004 | t0001 | g0034 | EUR | IBS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02074 | hp1 | a0001 | c0007 | t0001 | g0001 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02132 | hp1 | a0001 | c0012 | t0003 | g0117 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02145 | hp2 | a0004 | c0005 | t0001 | g0050 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CDX | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CDX | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | KHV | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02602 | hp2 | a0001 | c0008 | t0001 | g0156 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0167 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0030 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0279 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0266 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02723 | hp2 | a0001 | c0010 | t0001 | g0165 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0178 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02965 | hp1 | a0004 | c0005 | t0001 | g0049 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02965 | hp2 | a0007 | c0013 | t0001 | g0294 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0189 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03491 | hp2 | a0003 | c0004 | t0001 | g0213 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03492 | hp2 | a0003 | c0004 | t0001 | g0034 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0176 | SAS | STU | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0118 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0120 | SAS | BEB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0199 | SAS | BEB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | BEB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0185 | SAS | BEB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | STU | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | STU | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | STU | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | STU | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | STU | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | YRI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | YRI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | CHB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | YRI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18939 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18943 | hp2 | a0005 | c0006 | t0001 | g0012 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18946 | hp1 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18974 | hp1 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18983 | hp2 | a0002 | c0003 | t0001 | g0121 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18984 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18994 | hp1 | a0008 | c0009 | t0001 | g0219 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18998 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19005 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19009 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19010 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19011 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19012 | hp1 | a0005 | c0006 | t0001 | g0137 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | LWK | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19060 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19074 | hp2 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19090 | hp1 | a0002 | c0003 | t0001 | g0113 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | YRI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | ASW | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | ASW | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0278 | EUR | TSI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | TSI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0010 | EUR | TSI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | GIH | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | GIH | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ACB | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | USA | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | USA | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | LWK | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | LWK | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0208 | REF | REF | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0035 | REF | REF | TSPAN32_chr11_2297013_2323204 | TSPAN32 | chr11 | 2297013 | 2323204 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:2302165 | C | T | 1 | a0007 | 1 | HG02965.hp2 | stop_gained | HIGH | c.16C>T | p.Arg6* | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/10 | 153/1380 | 16/963 | 6/320 | chr11 | 2302165 | |||
chr11:2304154 | G | A | 1 | a0004 | 2 | HG02145.hp2 HG02965.hp1 |
missense_variant | MODERATE | c.229G>A | p.Val77Met | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/10 | 366/1380 | 229/963 | 77/320 | chr11 | 2304154 | |||
chr11:2304194 | T | G | 1 | a0008 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.269T>G | p.Leu90Arg | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/10 | 406/1380 | 269/963 | 90/320 | chr11 | 2304194 | |||
chr11:2313663 | G | A | 1 | a0002 | 14 | NA18939.hp1 NA18946.hp1 NA18967.hp2 others(11): Show |
missense_variant | MODERATE | c.364G>A | p.Ala122Thr | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/10 | 501/1380 | 364/963 | 122/320 | chr11 | 2313663 | |||
chr11:2314518 | C | T | 1 | a0003 | 5 | HG01256.hp2 HG01258.hp2 HG01516.hp1 others(2): Show |
missense_variant | MODERATE | c.490C>T | p.Arg164Cys | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/10 | 627/1380 | 490/963 | 164/320 | chr11 | 2314518 | |||
chr11:2316304 | G | T | 1 | a0005 | 2 | NA18943.hp2 NA19012.hp1 |
missense_variant | MODERATE | c.619G>T | p.Ala207Ser | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 7/10 | 756/1380 | 619/963 | 207/320 | chr11 | 2316304 | |||
chr11:2317881 | G | A | 1 | a0006 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.920G>A | p.Arg307His | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 10/10 | 1057/1380 | 920/963 | 307/320 | chr11 | 2317881 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:2302858 | T | G | 1 | a0001c0007 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.81T>G | p.Ser27Ser | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/10 | 218/1380 | 81/963 | 27/320 | chr11 | 2302858 | |||
chr11:2302918 | G | A | 1 | a0001c0008 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.141G>A | p.Ala47Ala | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/10 | 278/1380 | 141/963 | 47/320 | chr11 | 2302918 | |||
chr11:2308765 | C | T | 7 | a0001c0002 a0001c0012 a0002c0003 others(4): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
synonymous_variant | LOW | c.309C>T | p.Cys103Cys | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/10 | 446/1380 | 309/963 | 103/320 | chr11 | 2308765 | |||
chr11:2317882 | C | A | 1 | a0001c0010 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.921C>A | p.Arg307Arg | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 10/10 | 1058/1380 | 921/963 | 307/320 | chr11 | 2317882 | |||
chr11:2317888 | G | A | 1 | a0001c0012 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.927G>A | p.Gly309Gly | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 10/10 | 1064/1380 | 927/963 | 309/320 | chr11 | 2317888 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:2317965 | G | A | 2 | a0001c0001t0002 a0001c0002t0002 |
4 | HG01891.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*41G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 10/10 | 41 | chr11 | 2317965 | ||||||
chr11:2318006 | G | A | 1 | a0001c0012t0003 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*82G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 10/10 | 82 | chr11 | 2318006 | ||||||
chr11:2318113 | A | G | 1 | a0001c0001t0004 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 10/10 | 189 | chr11 | 2318113 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:2302298 | T | C | 197 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0027 others(194): Show |
249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.66+83T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302298 | |||||||
chr11:2302358 | C | T | 7 | a0001c0001t0001g0295 a0001c0002t0001g0289 a0001c0002t0001g0290 others(4): Show |
7 | HG02280.hp2 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+143C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302358 | |||||||
chr11:2302372 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.66+157C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302372 | |||||||
chr11:2302389 | G | T | 89 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0139 others(86): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.66+174G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302389 | |||||||
chr11:2302398 | T | C | 6 | a0001c0001t0001g0139 a0001c0002t0001g0140 a0001c0002t0001g0141 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+183T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302398 | |||||||
chr11:2302409 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+194G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302409 | |||||||
chr11:2302450 | T | C | 2 | a0004c0005t0001g0049 a0004c0005t0001g0050 |
2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.66+235T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302450 | |||||||
chr11:2302471 | G | A | 2 | a0001c0002t0001g0051 a0001c0002t0001g0052 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.66+256G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302471 | |||||||
chr11:2302552 | G | GTGGGGCT others(10): Show |
1 | a0001c0001t0001g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.67-291_67-275dupTG others(15): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 2302552 | ||||||
chr11:2302659 | G | T | 1 | a0001c0002t0001g0138 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.67-185G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302659 | |||||||
chr11:2302666 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.67-178C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302666 | |||||||
chr11:2302740 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.67-104G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302740 | |||||||
chr11:2302811 | A | G | 227 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(224): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.67-33A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 1/9 | chr11 | 2302811 | |||||||
chr11:2303078 | G | C | 1 | a0001c0002t0001g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.181+120G>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303078 | |||||||
chr11:2303092 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.181+134G>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303092 | |||||||
chr11:2303101 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0264 a0001c0001t0001g0265 |
5 | NA18942.hp2 NA18966.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+143G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303101 | |||||||
chr11:2303117 | T | C | 54 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0027 others(51): Show |
64 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.181+159T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303117 | |||||||
chr11:2303172 | G | A | 2 | a0004c0005t0001g0049 a0004c0005t0001g0050 |
2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.181+214G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303172 | |||||||
chr11:2303210 | C | T | 76 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0084 others(73): Show |
106 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.181+252C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303210 | |||||||
chr11:2303373 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.181+415G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303373 | |||||||
chr11:2303377 | T | G | 1 | a0001c0001t0001g0217 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.181+419T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303377 | |||||||
chr11:2303462 | C | T | 48 | a0001c0001t0001g0031 a0001c0001t0001g0181 a0001c0001t0001g0182 others(45): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.181+504C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303462 | |||||||
chr11:2303531 | G | A | 10 | a0001c0001t0001g0015 a0001c0001t0001g0267 a0001c0001t0001g0295 others(7): Show |
12 | HG01884.hp1 HG02280.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.181+573G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303531 | |||||||
chr11:2303576 | A | C | 4 | a0001c0002t0001g0012 a0001c0002t0001g0136 a0005c0006t0001g0012 others(1): Show |
5 | NA18943.hp2 NA18999.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-531A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303576 | |||||||
chr11:2303580 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0056 others(11): Show |
18 | HG00642.hp2 HG01109.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.182-527C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303580 | |||||||
chr11:2303586 | G | A | 2 | a0004c0005t0001g0049 a0004c0005t0001g0050 |
2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.182-521G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303586 | |||||||
chr11:2303622 | A | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
407 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(404): Show |
intron_variant | MODIFIER | c.182-485A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303622 | |||||||
chr11:2303773 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.182-334G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303773 | |||||||
chr11:2303878 | T | G | 208 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(205): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.182-229T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303878 | |||||||
chr11:2303962 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.182-145G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2303962 | |||||||
chr11:2304009 | C | T | 6 | a0001c0001t0001g0079 a0001c0002t0001g0016 a0001c0002t0001g0077 others(3): Show |
7 | HG01516.hp2 HG01517.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.182-98C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 2/9 | chr11 | 2304009 | |||||||
chr11:2304206 | T | A | 1 | a0008c0009t0001g0219 | 1 | NA18994.hp1 | splice_donor_variant&intron_variant | HIGH | c.279+2T>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304206 | |||||||
chr11:2304211 | T | G | 1 | a0008c0009t0001g0219 | 1 | NA18994.hp1 | splice_region_variant&intron_variant | LOW | c.279+7T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304211 | |||||||
chr11:2304214 | T | G | 1 | a0008c0009t0001g0219 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.279+10T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304214 | |||||||
chr11:2304215 | T | G | 1 | a0008c0009t0001g0219 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.279+11T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304215 | |||||||
chr11:2304217 | T | G | 1 | a0008c0009t0001g0219 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.279+13T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304217 | |||||||
chr11:2304223 | C | A | 1 | a0008c0009t0001g0219 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.279+19C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304223 | |||||||
chr11:2304224 | A | G | 1 | a0008c0009t0001g0219 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.279+20A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304224 | |||||||
chr11:2304238 | C | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.279+34C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304238 | |||||||
chr11:2304288 | C | T | 4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(1): Show |
4 | NA18969.hp2 NA18977.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+84C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304288 | |||||||
chr11:2304351 | C | T | 77 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0084 others(74): Show |
107 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.279+147C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304351 | |||||||
chr11:2304478 | C | T | 4 | a0003c0004t0001g0034 a0003c0004t0001g0211 a0003c0004t0001g0212 others(1): Show |
5 | HG01256.hp2 HG01258.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+274C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304478 | |||||||
chr11:2304499 | C | A | 5 | a0001c0002t0001g0028 a0001c0002t0001g0172 a0001c0002t0001g0173 others(2): Show |
6 | HG01070.hp1 HG02257.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+295C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304499 | |||||||
chr11:2304567 | CTA | C | 203 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(200): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.279+365_279+366del others(2): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2304567 | ||||||
chr11:2304570 | T | A | 203 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(200): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.279+366T>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304570 | |||||||
chr11:2304638 | T | A | 203 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(200): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.279+434T>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304638 | |||||||
chr11:2304671 | C | T | 203 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(200): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.279+467C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304671 | |||||||
chr11:2304753 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.279+549C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304753 | |||||||
chr11:2304767 | C | T | 30 | a0001c0001t0001g0027 a0001c0001t0001g0148 a0001c0001t0001g0149 others(27): Show |
36 | HG00639.hp1 HG00642.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.279+563C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304767 | |||||||
chr11:2304851 | C | A | 10 | a0001c0001t0001g0015 a0001c0001t0001g0267 a0001c0001t0001g0295 others(7): Show |
12 | HG01884.hp1 HG02280.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.279+647C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304851 | |||||||
chr11:2304899 | T | C | 206 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(203): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.279+695T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304899 | |||||||
chr11:2304907 | C | A | 1 | a0001c0002t0001g0176 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.279+703C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2304907 | |||||||
chr11:2305175 | C | T | 1 | a0001c0002t0001g0133 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.279+971C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305175 | |||||||
chr11:2305221 | T | G | 207 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(204): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.279+1017T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305221 | |||||||
chr11:2305370 | G | GC | 60 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0048 others(57): Show |
64 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.279+1177dupC | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2305370 | ||||||
chr11:2305370 | G | GCC | 18 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0056 others(15): Show |
23 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.279+1176_279+1177d others(4): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2305370 | ||||||
chr11:2305370 | G | GCCC | 43 | a0001c0001t0001g0031 a0001c0001t0001g0058 a0001c0001t0001g0139 others(40): Show |
53 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.279+1175_279+1177d others(5): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2305370 | ||||||
chr11:2305376 | C | CG | 6 | a0001c0002t0001g0008 a0001c0002t0001g0024 a0001c0002t0001g0131 others(3): Show |
10 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.279+1172_279+1173i others(3): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305376 | |||||||
chr11:2305378 | C | CA | 19 | a0001c0001t0001g0005 a0001c0001t0001g0268 a0001c0001t0001g0269 others(16): Show |
26 | HG00323.hp2 HG00558.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.279+1174_279+1175i others(3): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305378 | |||||||
chr11:2305382 | A | C | 42 | a0001c0001t0001g0027 a0001c0001t0001g0148 a0001c0001t0001g0149 others(39): Show |
50 | HG00639.hp1 HG00642.hp1 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.279+1178A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305382 | |||||||
chr11:2305384 | A | G | 42 | a0001c0001t0001g0027 a0001c0001t0001g0148 a0001c0001t0001g0149 others(39): Show |
50 | HG00639.hp1 HG00642.hp1 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.279+1180A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305384 | |||||||
chr11:2305427 | T | C | 207 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(204): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.279+1223T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305427 | |||||||
chr11:2305484 | A | G | 167 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(164): Show |
213 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.279+1280A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305484 | |||||||
chr11:2305504 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.279+1300G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305504 | |||||||
chr11:2305512 | G | A | 10 | a0001c0001t0001g0015 a0001c0001t0001g0267 a0001c0001t0001g0295 others(7): Show |
12 | HG01884.hp1 HG02280.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.279+1308G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305512 | |||||||
chr11:2305570 | G | A | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1366G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305570 | |||||||
chr11:2305675 | C | T | 2 | a0001c0002t0001g0051 a0001c0002t0001g0052 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.279+1471C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305675 | |||||||
chr11:2305690 | C | G | 89 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0061 others(86): Show |
118 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.279+1486C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305690 | |||||||
chr11:2305921 | T | C | 206 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(203): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.279+1717T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305921 | |||||||
chr11:2305958 | G | A | 206 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(203): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.279+1754G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305958 | |||||||
chr11:2305960 | C | T | 53 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0181 others(50): Show |
66 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.279+1756C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305960 | |||||||
chr11:2305972 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0123 |
2 | HG01346.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.279+1768G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2305972 | |||||||
chr11:2306007 | AGT | A | 43 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0148 others(40): Show |
53 | HG00639.hp1 HG00642.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.279+1813_279+1814d others(4): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306007 | ||||||
chr11:2306044 | C | CTGTGTGT others(9): Show |
2 | a0002c0003t0001g0121 a0002c0003t0001g0122 |
2 | NA18946.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.279+1841_279+1842i others(18): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306044 | ||||||
chr11:2306044 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0002g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.279+1841_279+1842i others(22): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306044 | ||||||
chr11:2306046 | C | CTG | 6 | a0001c0001t0001g0139 a0001c0001t0001g0255 a0001c0001t0001g0256 others(3): Show |
6 | HG02055.hp1 HG02738.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1866_279+1867d others(4): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTG | 6 | a0001c0001t0001g0054 a0001c0001t0001g0267 a0001c0002t0001g0087 others(3): Show |
6 | HG01069.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+1864_279+1867d others(6): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTG | 34 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0001t0001g0058 others(31): Show |
45 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.279+1862_279+1867d others(8): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTGT others(1): Show |
19 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0057 others(16): Show |
21 | HG00741.hp1 HG01081.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+1860_279+1867d others(10): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTGT others(3): Show |
32 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(29): Show |
41 | HG00639.hp1 HG00642.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.279+1858_279+1867d others(12): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTGT others(5): Show |
4 | a0001c0001t0001g0064 a0001c0002t0001g0053 a0001c0002t0001g0078 others(1): Show |
4 | HG01884.hp2 HG02615.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+1856_279+1867d others(14): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTGT others(7): Show |
12 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(9): Show |
12 | HG00738.hp1 HG01074.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.279+1854_279+1867d others(16): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTGT others(9): Show |
52 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0069 others(49): Show |
77 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.279+1852_279+1867d others(18): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTGT others(11): Show |
19 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0115 others(16): Show |
23 | HG00741.hp2 HG01071.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.279+1850_279+1867d others(20): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTGT others(13): Show |
15 | a0001c0001t0001g0031 a0001c0001t0001g0181 a0001c0001t0001g0182 others(12): Show |
18 | HG00423.hp1 HG00609.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.279+1848_279+1867d others(22): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTGT others(15): Show |
5 | a0001c0001t0001g0184 a0001c0002t0001g0185 a0001c0002t0001g0205 others(2): Show |
5 | HG00544.hp2 HG03654.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+1846_279+1867d others(24): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | CTGTGTGT others(17): Show |
1 | a0001c0002t0001g0209 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.279+1844_279+1867d others(26): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306046 | ||||||
chr11:2306046 | C | G | 3 | a0001c0001t0002g0210 a0002c0003t0001g0121 a0002c0003t0001g0122 |
3 | HG02976.hp2 NA18946.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.279+1842C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306046 | |||||||
chr11:2306047 | T | TGTGTGTG others(5): Show |
1 | a0001c0002t0001g0147 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.279+1854_279+1855i others(14): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306047 | ||||||
chr11:2306086 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0123 |
2 | HG01346.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.279+1882G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306086 | |||||||
chr11:2306108 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0123 |
2 | HG01346.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.279+1904C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306108 | |||||||
chr11:2306164 | G | A | 2 | a0001c0002t0001g0019 a0001c0002t0001g0091 |
3 | HG00544.hp1 NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.279+1960G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306164 | |||||||
chr11:2306281 | C | T | 2 | a0001c0002t0001g0154 a0001c0002t0001g0157 |
2 | HG01192.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.279+2077C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306281 | |||||||
chr11:2306306 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.279+2102G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306306 | |||||||
chr11:2306357 | C | T | 202 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0027 others(199): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.279+2153C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306357 | |||||||
chr11:2306371 | C | G | 48 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0001c0001t0001g0183 others(45): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.279+2167C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306371 | |||||||
chr11:2306476 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
5 | HG02015.hp2 NA18948.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-2260C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306476 | |||||||
chr11:2306501 | C | T | 2 | a0001c0002t0001g0051 a0001c0002t0001g0052 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.280-2235C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306501 | |||||||
chr11:2306544 | G | GGAGA | 5 | a0001c0002t0001g0028 a0001c0002t0001g0172 a0001c0002t0001g0173 others(2): Show |
6 | HG01070.hp1 HG02257.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-2185_280-2182d others(6): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306544 | ||||||
chr11:2306547 | GAGAGAGA others(1): Show |
G | 18 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.280-2165_280-2158d others(10): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306547 | ||||||
chr11:2306551 | GAGAA | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0083 others(70): Show |
99 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.280-2181_280-2178d others(6): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306551 | ||||||
chr11:2306555 | A | G | 1 | a0005c0006t0001g0137 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.280-2181A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306555 | |||||||
chr11:2306561 | G | A | 1 | a0002c0003t0001g0111 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.280-2175G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306561 | |||||||
chr11:2306563 | A | G | 1 | a0002c0003t0001g0111 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.280-2173A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306563 | |||||||
chr11:2306799 | A | AAGGAGGG others(201): Show |
1 | a0001c0001t0001g0045 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.280-1790_280-1789i others(210): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306799 | ||||||
chr11:2306824 | AGAGGGAG others(5): Show |
A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0258 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.280-1900_280-1889d others(14): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306824 | ||||||
chr11:2306836 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.280-1900G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306836 | |||||||
chr11:2306836 | GGAGGGA | G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(170): Show |
220 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.280-1892_280-1887d others(8): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306836 | ||||||
chr11:2306839 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.280-1897G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306839 | |||||||
chr11:2306842 | A | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0250 a0001c0001t0001g0258 |
3 | HG03139.hp2 NA19000.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.280-1894A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306842 | |||||||
chr11:2306844 | A | G | 40 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0054 others(37): Show |
48 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.280-1892A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306844 | |||||||
chr11:2306863 | A | C | 1 | a0001c0001t0001g0280 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.280-1873A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306863 | |||||||
chr11:2306875 | G | A | 78 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0083 others(75): Show |
107 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.280-1861G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306875 | |||||||
chr11:2306916 | GAGGAGGA others(15): Show |
G | 2 | a0001c0001t0001g0216 a0001c0002t0001g0290 |
2 | HG02895.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.280-1810_280-1789d others(24): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306916 | ||||||
chr11:2306926 | T | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0039 others(122): Show |
164 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.280-1810T>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306926 | |||||||
chr11:2306935 | GGGAAGGA others(16): Show |
G | 1 | a0001c0002t0001g0112 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.280-1799_280-1777d others(25): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306935 | ||||||
chr11:2306947 | A | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0044 others(110): Show |
147 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.280-1789A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306947 | |||||||
chr11:2306948 | AGGAGGAG others(20): Show |
A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0044 others(110): Show |
147 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.280-1787_280-1761d others(29): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306948 | |||||||
chr11:2306958 | A | G | 114 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0027 others(111): Show |
134 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.280-1778A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306958 | |||||||
chr11:2306963 | G | A | 9 | a0001c0001t0001g0139 a0001c0002t0001g0141 a0001c0002t0001g0142 others(6): Show |
9 | HG02055.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.280-1773G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306963 | |||||||
chr11:2306967 | A | AGAAGGAG others(5): Show |
1 | a0001c0001t0001g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-1768_280-1767i others(14): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306967 | ||||||
chr11:2306970 | AAAGAG | A | 103 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0031 others(100): Show |
129 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.280-1763_280-1759d others(7): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2306970 | ||||||
chr11:2306972 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-1764A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2306972 | |||||||
chr11:2307134 | A | C | 206 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0027 others(203): Show |
264 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.280-1602A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307134 | |||||||
chr11:2307135 | G | A | 5 | a0001c0002t0001g0140 a0001c0002t0001g0141 a0001c0002t0001g0142 others(2): Show |
5 | HG02615.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-1601G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307135 | |||||||
chr11:2307182 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-1554C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307182 | |||||||
chr11:2307225 | G | A | 1 | a0001c0002t0001g0094 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.280-1511G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307225 | |||||||
chr11:2307345 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280-1391C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307345 | |||||||
chr11:2307398 | G | A | 1 | a0001c0002t0001g0291 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.280-1338G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307398 | |||||||
chr11:2307425 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.280-1311C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307425 | |||||||
chr11:2307426 | G | A | 4 | a0001c0002t0001g0012 a0001c0002t0001g0136 a0005c0006t0001g0012 others(1): Show |
5 | NA18943.hp2 NA18999.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-1310G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307426 | |||||||
chr11:2307437 | G | A | 4 | a0001c0001t0001g0183 a0001c0001t0001g0202 a0001c0001t0001g0254 others(1): Show |
4 | HG00423.hp1 HG02135.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-1299G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307437 | |||||||
chr11:2307463 | C | T | 216 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(213): Show |
275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.280-1273C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307463 | |||||||
chr11:2307477 | A | G | 207 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(204): Show |
266 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.280-1259A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307477 | |||||||
chr11:2307529 | G | A | 5 | a0001c0002t0001g0140 a0001c0002t0001g0141 a0001c0002t0001g0142 others(2): Show |
5 | HG02615.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-1207G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307529 | |||||||
chr11:2307533 | GC | G | 16 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0083 others(13): Show |
17 | HG00544.hp2 HG02109.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.280-1200delC | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2307533 | ||||||
chr11:2307565 | G | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(46): Show |
60 | HG00323.hp2 HG00558.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.280-1171G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307565 | |||||||
chr11:2307631 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.280-1105G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307631 | |||||||
chr11:2307718 | C | T | 144 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(141): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.280-1018C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307718 | |||||||
chr11:2307779 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.280-957G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307779 | |||||||
chr11:2307848 | T | G | 211 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(208): Show |
270 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.280-888T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307848 | |||||||
chr11:2307889 | C | T | 210 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(207): Show |
269 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.280-847C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2307889 | |||||||
chr11:2308004 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.280-732G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308004 | |||||||
chr11:2308193 | A | C | 210 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(207): Show |
269 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.280-543A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308193 | |||||||
chr11:2308200 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.280-536G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308200 | |||||||
chr11:2308227 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.280-509C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308227 | |||||||
chr11:2308235 | G | T | 1 | a0001c0002t0001g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.280-501G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308235 | |||||||
chr11:2308246 | C | G | 1 | a0007c0013t0001g0294 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.280-490C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308246 | |||||||
chr11:2308388 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.280-348C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308388 | |||||||
chr11:2308409 | CCCCCCAC others(128): Show |
C | 1 | a0001c0001t0001g0275 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280-321_280-187del | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308409 | ||||||
chr11:2308416 | C | CAGTGACC others(336): Show |
1 | a0001c0001t0001g0282 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.280-305_280-304ins others(343): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308416 | ||||||
chr11:2308416 | C | CAGTGACC others(129): Show |
1 | a0001c0001t0001g0220 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.280-228_280-93dupC others(135): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308416 | ||||||
chr11:2308416 | CAGTGACC others(129): Show |
C | 186 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(183): Show |
243 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.280-228_280-93del | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308416 | ||||||
chr11:2308426 | CCCCCCGC others(128): Show |
C | 1 | a0001c0002t0002g0167 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.280-304_280-170del | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308426 | ||||||
chr11:2308428 | CCCCGCAG others(126): Show |
C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0084 others(8): Show |
12 | HG02622.hp2 HG02897.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.280-304_280-172del | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308428 | ||||||
chr11:2308429 | CCCGCAGT others(125): Show |
C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0184 |
2 | HG00544.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.280-304_280-173del | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308429 | ||||||
chr11:2308432 | GCAGTGAC others(61): Show |
G | 1 | a0001c0001t0001g0240 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.280-236_280-169del others(68): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308432 | ||||||
chr11:2308463 | CCAACAGT others(235): Show |
C | 1 | a0001c0001t0001g0149 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280-255_280-14del | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308463 | ||||||
chr11:2308464 | C | G | 7 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0001g0123 others(4): Show |
7 | HG02056.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-272C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308464 | |||||||
chr11:2308494 | CCCCCCAC others(128): Show |
C | 3 | a0001c0001t0001g0074 a0001c0002t0001g0120 a0005c0006t0001g0137 |
3 | HG02809.hp1 HG03831.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.280-236_280-102del | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308494 | ||||||
chr11:2308500 | A | ACAGTGAC others(61): Show |
1 | a0001c0001t0001g0237 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.280-168_280-101dup others(68): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308500 | ||||||
chr11:2308500 | A | ACAGTGAC others(61): Show |
1 | a0001c0002t0001g0002 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.280-205_280-204ins others(68): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308500 | ||||||
chr11:2308500 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.280-236A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308500 | |||||||
chr11:2308508 | C | T | 3 | a0001c0001t0001g0060 a0001c0002t0001g0101 a0001c0002t0001g0112 |
3 | HG02056.hp1 HG03486.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.280-228C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308508 | |||||||
chr11:2308508 | CAGCCCCC others(129): Show |
C | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280-227_280-92del | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308508 | |||||||
chr11:2308509 | A | G | 3 | a0001c0001t0001g0060 a0001c0002t0001g0101 a0001c0002t0001g0112 |
3 | HG02056.hp1 HG03486.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.280-227A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308509 | |||||||
chr11:2308511 | CCCCCCGC others(26): Show |
C | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-219_280-187del others(33): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308511 | ||||||
chr11:2308515 | CCGCAATG others(128): Show |
C | 2 | a0001c0002t0001g0101 a0001c0002t0001g0112 |
2 | HG02056.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.280-219_280-85del | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308515 | ||||||
chr11:2308547 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-189C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308547 | |||||||
chr11:2308552 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0275 |
2 | HG01978.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.280-184T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308552 | |||||||
chr11:2308567 | C | A | 13 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
14 | HG00544.hp2 HG02622.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.280-169C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308567 | |||||||
chr11:2308572 | T | C | 14 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0083 others(11): Show |
15 | HG00544.hp2 HG02622.hp2 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-164T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308572 | |||||||
chr11:2308592 | C | A | 1 | a0001c0002t0001g0154 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.280-144C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308592 | |||||||
chr11:2308600 | C | A | 5 | a0001c0002t0001g0140 a0001c0002t0001g0141 a0001c0002t0001g0142 others(2): Show |
5 | HG02615.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-136C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308600 | |||||||
chr11:2308600 | C | G | 183 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(180): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.280-136C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308600 | |||||||
chr11:2308611 | A | G | 2 | a0001c0001t0001g0241 a0001c0002t0001g0106 |
2 | HG02148.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.280-125A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308611 | |||||||
chr11:2308617 | C | T | 2 | a0001c0002t0001g0055 a0001c0002t0001g0169 |
2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.280-119C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308617 | |||||||
chr11:2308627 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.280-109C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308627 | |||||||
chr11:2308650 | G | C | 207 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(204): Show |
266 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.280-86G>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308650 | |||||||
chr11:2308664 | GC | G | 203 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(200): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.280-64delC | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 2308664 | ||||||
chr11:2308672 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.280-64C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308672 | |||||||
chr11:2308679 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0139 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.280-57G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308679 | |||||||
chr11:2308690 | C | G | 1 | a0001c0002t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.280-46C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308690 | |||||||
chr11:2308706 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280-30C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 3/9 | chr11 | 2308706 | |||||||
chr11:2308842 | A | C | 1 | a0001c0002t0001g0114 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.354+32A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2308842 | |||||||
chr11:2308847 | C | G | 141 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(138): Show |
188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.354+37C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2308847 | |||||||
chr11:2309170 | G | A | 209 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(206): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.354+360G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309170 | |||||||
chr11:2309249 | G | A | 209 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(206): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.354+439G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309249 | |||||||
chr11:2309288 | G | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0048 others(37): Show |
49 | HG00323.hp2 HG00558.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.354+478G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309288 | |||||||
chr11:2309333 | C | A | 1 | a0001c0002t0001g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.354+523C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309333 | |||||||
chr11:2309333 | C | T | 139 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(136): Show |
186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.354+523C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309333 | |||||||
chr11:2309334 | G | T | 1 | a0001c0002t0001g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.354+524G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309334 | |||||||
chr11:2309335 | T | G | 1 | a0001c0002t0001g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.354+525T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309335 | |||||||
chr11:2309347 | A | T | 1 | a0001c0002t0001g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.354+537A>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309347 | |||||||
chr11:2309366 | C | T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(42): Show |
56 | HG00323.hp2 HG00558.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.354+556C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309366 | |||||||
chr11:2309380 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0139 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.354+570G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309380 | |||||||
chr11:2309404 | C | A | 1 | a0001c0002t0001g0016 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.354+594C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309404 | |||||||
chr11:2309417 | G | T | 1 | a0001c0001t0001g0248 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.354+607G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309417 | |||||||
chr11:2309424 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354+614G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309424 | |||||||
chr11:2309536 | G | A | 2 | a0001c0001t0001g0267 a0004c0005t0001g0050 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.354+726G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309536 | |||||||
chr11:2309571 | G | A | 1 | a0001c0002t0001g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.354+761G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309571 | |||||||
chr11:2309652 | G | T | 1 | a0001c0002t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.354+842G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309652 | |||||||
chr11:2309689 | A | C | 16 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0083 others(13): Show |
17 | HG00544.hp2 HG02109.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.354+879A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309689 | |||||||
chr11:2309700 | C | T | 209 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(206): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.354+890C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309700 | |||||||
chr11:2309745 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.354+935C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309745 | |||||||
chr11:2309747 | T | C | 209 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(206): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.354+937T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309747 | |||||||
chr11:2309820 | C | A | 209 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(206): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.354+1010C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309820 | |||||||
chr11:2309823 | A | G | 209 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(206): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.354+1013A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309823 | |||||||
chr11:2309838 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.354+1028G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309838 | |||||||
chr11:2309866 | G | A | 209 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(206): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.354+1056G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309866 | |||||||
chr11:2309984 | A | C | 209 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(206): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.354+1174A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2309984 | |||||||
chr11:2310001 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.354+1191C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310001 | |||||||
chr11:2310077 | G | C | 207 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(204): Show |
265 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.354+1267G>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310077 | |||||||
chr11:2310186 | G | A | 18 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0083 others(15): Show |
19 | HG00544.hp2 HG02109.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.354+1376G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310186 | |||||||
chr11:2310214 | G | T | 145 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(142): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.354+1404G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310214 | |||||||
chr11:2310317 | G | A | 107 | a0001c0001t0001g0241 a0001c0002t0001g0002 a0001c0002t0001g0003 others(104): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.354+1507G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310317 | |||||||
chr11:2310334 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.354+1524G>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310334 | |||||||
chr11:2310367 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0037 others(35): Show |
52 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.354+1557G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310367 | |||||||
chr11:2310432 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.354+1622C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310432 | |||||||
chr11:2310599 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.354+1789G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310599 | |||||||
chr11:2310635 | C | T | 2 | a0001c0001t0001g0267 a0004c0005t0001g0050 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.354+1825C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310635 | |||||||
chr11:2310643 | G | T | 1 | a0001c0002t0001g0199 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.354+1833G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310643 | |||||||
chr11:2310807 | G | A | 157 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0083 others(154): Show |
205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.354+1997G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310807 | |||||||
chr11:2310826 | G | T | 1 | a0001c0001t0001g0232 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.354+2016G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310826 | |||||||
chr11:2310884 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.354+2074C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310884 | |||||||
chr11:2310885 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0148 |
4 | HG01884.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+2075G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2310885 | |||||||
chr11:2311192 | C | A | 2 | a0001c0001t0001g0267 a0004c0005t0001g0050 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.354+2382C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311192 | |||||||
chr11:2311202 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.354+2392C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311202 | |||||||
chr11:2311232 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0102 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.354+2422G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311232 | |||||||
chr11:2311436 | G | T | 3 | a0001c0002t0001g0016 a0001c0002t0001g0077 a0001c0002t0001g0078 |
4 | HG01516.hp2 HG01517.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-2218G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311436 | |||||||
chr11:2311440 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.355-2214C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311440 | |||||||
chr11:2311464 | A | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(50): Show |
64 | HG00323.hp2 HG00558.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.355-2190A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311464 | |||||||
chr11:2311479 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.355-2175G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311479 | |||||||
chr11:2311496 | G | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0048 others(37): Show |
49 | HG00323.hp2 HG00558.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.355-2158G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311496 | |||||||
chr11:2311693 | G | A | 2 | a0001c0002t0001g0029 a0001c0002t0001g0196 |
3 | HG03490.hp2 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.355-1961G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311693 | |||||||
chr11:2311894 | G | A | 156 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0083 others(153): Show |
204 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.355-1760G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311894 | |||||||
chr11:2311908 | C | T | 1 | a0001c0002t0001g0204 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.355-1746C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311908 | |||||||
chr11:2311939 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.355-1715C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2311939 | |||||||
chr11:2312005 | C | CAGAGCCA others(12): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0148 |
4 | HG01884.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-1630_355-1612d others(21): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 2312005 | ||||||
chr11:2312035 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.355-1619A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312035 | |||||||
chr11:2312047 | G | GCAGGCAG others(12): Show |
15 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0083 others(12): Show |
16 | HG00544.hp2 HG02135.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-1587_355-1569d others(21): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 2312047 | ||||||
chr11:2312135 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.355-1519A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312135 | |||||||
chr11:2312196 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.355-1458G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312196 | |||||||
chr11:2312261 | C | A | 3 | a0001c0002t0001g0168 a0001c0002t0001g0187 a0001c0002t0001g0191 |
3 | HG02451.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.355-1393C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312261 | |||||||
chr11:2312371 | C | A | 1 | a0001c0002t0001g0290 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.355-1283C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312371 | |||||||
chr11:2312435 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.355-1219C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312435 | |||||||
chr11:2312445 | A | G | 120 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0038 others(117): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.355-1209A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312445 | |||||||
chr11:2312616 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0238 |
6 | NA18978.hp2 NA18982.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-1038C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312616 | |||||||
chr11:2312630 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(62): Show |
113 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.355-1024G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312630 | |||||||
chr11:2312680 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0148 |
4 | HG01884.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-974G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312680 | |||||||
chr11:2312757 | T | C | 6 | a0001c0001t0001g0076 a0001c0001t0001g0139 a0001c0002t0001g0072 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-897T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312757 | |||||||
chr11:2312760 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.355-894G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312760 | |||||||
chr11:2312809 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0031 others(52): Show |
66 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.355-845T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312809 | |||||||
chr11:2312879 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.355-775C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312879 | |||||||
chr11:2312880 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.355-774G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312880 | |||||||
chr11:2312898 | A | G | 2 | a0001c0001t0001g0054 a0001c0002t0001g0266 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.355-756A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312898 | |||||||
chr11:2312905 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.355-749C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312905 | |||||||
chr11:2312972 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.355-682G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2312972 | |||||||
chr11:2313057 | C | G | 1 | a0001c0002t0001g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.355-597C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313057 | |||||||
chr11:2313080 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.355-574C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313080 | |||||||
chr11:2313085 | C | T | 8 | a0001c0001t0001g0149 a0001c0002t0001g0026 a0001c0002t0001g0289 others(5): Show |
9 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.355-569C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313085 | |||||||
chr11:2313106 | C | T | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(5): Show |
8 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-548C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313106 | |||||||
chr11:2313174 | G | A | 2 | a0001c0001t0001g0039 a0008c0009t0001g0219 |
3 | NA18945.hp1 NA18965.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.355-480G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313174 | |||||||
chr11:2313175 | C | A | 2 | a0001c0001t0001g0039 a0008c0009t0001g0219 |
3 | NA18945.hp1 NA18965.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.355-479C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313175 | |||||||
chr11:2313177 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0002g0210 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.355-477C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313177 | |||||||
chr11:2313208 | GGGAAAGA others(12): Show |
G | 1 | a0001c0001t0001g0092 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.355-445_355-427del others(19): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313208 | |||||||
chr11:2313437 | T | C | 1 | a0001c0002t0001g0157 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.355-217T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313437 | |||||||
chr11:2313501 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.355-153C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313501 | |||||||
chr11:2313503 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.355-151G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313503 | |||||||
chr11:2313510 | G | A | 121 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0057 others(118): Show |
160 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.355-144G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313510 | |||||||
chr11:2313573 | C | T | 1 | a0001c0002t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.355-81C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 4/9 | chr11 | 2313573 | |||||||
chr11:2313765 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.456+10G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2313765 | |||||||
chr11:2313785 | C | T | 6 | a0001c0002t0001g0008 a0001c0002t0001g0024 a0001c0002t0001g0028 others(3): Show |
11 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.456+30C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2313785 | |||||||
chr11:2313807 | C | A | 1 | a0001c0001t0001g0234 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.456+52C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2313807 | |||||||
chr11:2313957 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.456+202C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2313957 | |||||||
chr11:2313965 | A | C | 10 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0139 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.456+210A>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2313965 | |||||||
chr11:2313975 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.456+220G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2313975 | |||||||
chr11:2314036 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.456+281G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314036 | |||||||
chr11:2314049 | G | A | 6 | a0001c0001t0001g0149 a0001c0002t0001g0051 a0001c0002t0001g0140 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.456+294G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314049 | |||||||
chr11:2314113 | A | G | 2 | a0001c0001t0001g0056 a0001c0002t0001g0266 |
2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.456+358A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314113 | |||||||
chr11:2314162 | T | TA | 161 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(158): Show |
220 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.457-307dupA | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 2314162 | ||||||
chr11:2314162 | T | TAA | 9 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0166 others(6): Show |
9 | HG01255.hp1 HG02559.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.457-308_457-307dup others(2): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 2314162 | ||||||
chr11:2314162 | TA | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0061 others(11): Show |
17 | HG00558.hp2 HG01256.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.457-307delA | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 2314162 | ||||||
chr11:2314179 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.457-306G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314179 | |||||||
chr11:2314184 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.457-301G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314184 | |||||||
chr11:2314186 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.457-299A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314186 | |||||||
chr11:2314206 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0220 a0001c0001t0001g0258 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.457-279C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314206 | |||||||
chr11:2314214 | C | G | 125 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0064 others(122): Show |
169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.457-271C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314214 | |||||||
chr11:2314259 | T | C | 1 | a0001c0002t0001g0192 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.457-226T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314259 | |||||||
chr11:2314311 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0201 |
3 | NA18945.hp2 NA18971.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.457-174C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314311 | |||||||
chr11:2314330 | G | A | 3 | a0001c0001t0002g0210 a0001c0002t0002g0017 a0001c0002t0002g0167 |
4 | HG01891.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.457-155G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 5/9 | chr11 | 2314330 | |||||||
chr11:2314578 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.543+7G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2314578 | |||||||
chr11:2314610 | C | T | 3 | a0001c0001t0002g0210 a0001c0002t0002g0017 a0001c0002t0002g0167 |
4 | HG01891.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+39C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2314610 | |||||||
chr11:2314702 | T | C | 1 | a0001c0002t0001g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+131T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2314702 | |||||||
chr11:2314750 | CATGGTAC others(11): Show |
C | 1 | a0001c0001t0001g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.543+180_543+197del others(18): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2314750 | |||||||
chr11:2314812 | G | C | 6 | a0001c0002t0001g0008 a0001c0002t0001g0024 a0001c0002t0001g0028 others(3): Show |
11 | HG01243.hp2 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+241G>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2314812 | |||||||
chr11:2314894 | C | T | 2 | a0001c0001t0001g0056 a0001c0002t0001g0266 |
2 | HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.543+323C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2314894 | |||||||
chr11:2314978 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.543+407G>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2314978 | |||||||
chr11:2315034 | A | AGCCAGGC others(12): Show |
122 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0064 others(119): Show |
165 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.543+464_543+465ins others(19): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 2315034 | ||||||
chr11:2315034 | A | AGCGAGGC others(12): Show |
93 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(90): Show |
111 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.543+464_543+465ins others(19): Show |
TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 2315034 | ||||||
chr11:2315152 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.543+581G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315152 | |||||||
chr11:2315202 | C | T | 1 | a0001c0002t0001g0104 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.543+631C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315202 | |||||||
chr11:2315235 | C | G | 1 | a0001c0001t0001g0237 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.543+664C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315235 | |||||||
chr11:2315388 | T | C | 1 | a0001c0001t0001g0040 | 2 | HG00438.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.543+817T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315388 | |||||||
chr11:2315447 | C | T | 2 | a0001c0001t0001g0150 a0001c0008t0001g0156 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.544-782C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315447 | |||||||
chr11:2315605 | C | A | 2 | a0001c0002t0001g0172 a0001c0002t0001g0174 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.544-624C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315605 | |||||||
chr11:2315645 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-584C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315645 | |||||||
chr11:2315782 | G | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
407 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(404): Show |
intron_variant | MODIFIER | c.544-447G>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315782 | |||||||
chr11:2315792 | T | C | 4 | a0001c0001t0002g0210 a0001c0002t0001g0073 a0001c0002t0002g0017 others(1): Show |
5 | HG01891.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-437T>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315792 | |||||||
chr11:2315988 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(30): Show |
67 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.544-241G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315988 | |||||||
chr11:2315991 | C | T | 5 | a0001c0002t0001g0077 a0001c0002t0001g0078 a0001c0002t0001g0080 others(2): Show |
5 | HG02004.hp1 HG02602.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-238C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2315991 | |||||||
chr11:2316042 | G | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0054 others(18): Show |
26 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-187G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2316042 | |||||||
chr11:2316097 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.544-132T>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2316097 | |||||||
chr11:2316104 | C | T | 2 | a0001c0002t0001g0172 a0001c0002t0001g0174 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.544-125C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 6/9 | chr11 | 2316104 | |||||||
chr11:2316420 | C | T | 1 | a0001c0002t0001g0193 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.627+108C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 7/9 | chr11 | 2316420 | |||||||
chr11:2316463 | G | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(64): Show |
83 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.628-113G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 7/9 | chr11 | 2316463 | |||||||
chr11:2316528 | C | T | 6 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0139 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-48C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 7/9 | chr11 | 2316528 | |||||||
chr11:2316533 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.628-43G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 7/9 | chr11 | 2316533 | |||||||
chr11:2316556 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.628-20C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 7/9 | chr11 | 2316556 | |||||||
chr11:2316808 | G | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0054 others(18): Show |
26 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.719+141G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2316808 | |||||||
chr11:2316813 | G | A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0139 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.719+146G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2316813 | |||||||
chr11:2316861 | C | T | 2 | a0001c0002t0001g0172 a0001c0002t0001g0174 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.719+194C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2316861 | |||||||
chr11:2316879 | T | A | 1 | a0001c0002t0001g0278 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.719+212T>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2316879 | |||||||
chr11:2316885 | C | A | 1 | a0001c0001t0001g0257 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.719+218C>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2316885 | |||||||
chr11:2316904 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.719+237A>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2316904 | |||||||
chr11:2317010 | A | T | 119 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0068 others(116): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.720-334A>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2317010 | |||||||
chr11:2317026 | A | G | 208 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0015 others(205): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.720-318A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2317026 | |||||||
chr11:2317055 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.720-289G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2317055 | |||||||
chr11:2317151 | A | G | 6 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0139 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.720-193A>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2317151 | |||||||
chr11:2317156 | C | T | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.720-188C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2317156 | |||||||
chr11:2317167 | G | A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0139 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.720-177G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2317167 | |||||||
chr11:2317239 | A | T | 5 | a0001c0002t0001g0077 a0001c0002t0001g0078 a0001c0002t0001g0080 others(2): Show |
5 | HG02004.hp1 HG02602.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.720-105A>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2317239 | |||||||
chr11:2317286 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.720-58C>T | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2317286 | |||||||
chr11:2317299 | C | G | 2 | a0001c0001t0001g0064 a0001c0002t0001g0096 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.720-45C>G | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 8/9 | chr11 | 2317299 | |||||||
chr11:2317747 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.902-116G>A | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 9/9 | chr11 | 2317747 | |||||||
chr11:2317811 | G | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0054 others(18): Show |
26 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.902-52G>C | TSPAN32 | ENSG00000064201.16 | transcript | ENST00000182290.9 | protein_coding | 9/9 | chr11 | 2317811 |