Item | Value |
---|---|
geneid | 928 |
ensemblid | ENSG00000010278.15 |
hgncid | 1709 |
symbol | CD9 |
name | CD9 molecule |
refseq_nuc | NM_001769.4 |
refseq_prot | NP_001760.1 |
ensembl_nuc | ENST00000009180.10 |
ensembl_prot | ENSP00000009180.4 |
mane_status | MANE Select |
chr | chr12 |
start | 6200400 |
end | 6238266 |
strand | + |
ver | v1.2 |
region | chr12:6200400-6238266 |
region5000 | chr12:6195400-6243266 |
regionname0 | CD9_chr12_6200400_6238266 |
regionname5000 | CD9_chr12_6195400_6243266 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 228 | 375 | 92 | 62 | 171 | 8 | 40 | 135 | CD9_chr12_6195400_6243266 | CD9 | MPVKG others(223): Show |
chr12 | 6195400 | 6243266 |
a0002 | 0/0 | 228 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | MPVKG others(223): Show |
chr12 | 6195400 | 6243266 |
a0003 | 0/0 | 110 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | MPVKG others(105): Show |
chr12 | 6195400 | 6243266 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 684 | 370 | 90 | 62 | 169 | 8 | 39 | CD9_chr12_6195400_6243266 | CD9 | ATGCC others(679): Show |
chr12 | 6195400 | 6243266 | ||
a0001c0002 | 0/0 | 684 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | ATGCC others(679): Show |
chr12 | 6195400 | 6243266 | ||
a0001c0005 | 0/0 | 684 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | ATGCC others(679): Show |
chr12 | 6195400 | 6243266 | ||
a0001c0006 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | ATGCC others(679): Show |
chr12 | 6195400 | 6243266 | ||
a0001c0007 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | ATGCC others(679): Show |
chr12 | 6195400 | 6243266 | ||
a0002c0003 | 0/0 | 684 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | ATGCC others(679): Show |
chr12 | 6195400 | 6243266 | ||
a0003c0004 | 0/0 | 709 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | ATGCC others(704): Show |
chr12 | 6195400 | 6243266 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1225 | 321 | 54 | 57 | 165 | 7 | 36 | CD9_chr12_6195400_6243266 | CD9 | AGCCG others(1220): Show |
chr12 | 6195400 | 6243266 |
a0001c0001t0002 | 0/0 | 1225 | 48 | 35 | 5 | 4 | 1 | 3 | CD9_chr12_6195400_6243266 | CD9 | AGCCG others(1220): Show |
chr12 | 6195400 | 6243266 |
a0001c0001t0003 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | AGCCG others(1220): Show |
chr12 | 6195400 | 6243266 |
a0001c0002t0001 | 0/0 | 1225 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | AGCCG others(1220): Show |
chr12 | 6195400 | 6243266 |
a0001c0005t0001 | 0/0 | 1225 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | AGCCG others(1220): Show |
chr12 | 6195400 | 6243266 |
a0001c0006t0001 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | AGCCG others(1220): Show |
chr12 | 6195400 | 6243266 |
a0001c0007t0001 | 0/0 | 1225 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | AGCCG others(1220): Show |
chr12 | 6195400 | 6243266 |
a0002c0003t0001 | 0/0 | 1225 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | AGCCG others(1220): Show |
chr12 | 6195400 | 6243266 |
a0003c0004t0001 | 0/0 | 1250 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | AGCCG others(1245): Show |
chr12 | 6195400 | 6243266 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 2 | 2 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0004 | 1/0 | 7 | 0 | 2 | 1 | 0 | 3 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0005 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0006t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0001c0007t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0002c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0299 | EUR | IBS | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CDX | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02735 | hp2 | a0001 | c0005 | t0001 | g0228 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02976 | hp2 | a0001 | c0007 | t0001 | g0162 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03225 | hp1 | a0001 | c0006 | t0001 | g0189 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | BEB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18951 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18986 | hp1 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19075 | hp2 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ASW | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | TSI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | GIH | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | USA | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | USA | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | USA | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | LWK | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0155 | REF | REF | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | CD9_chr12_6195400_6243266 | CD9 | chr12 | 6195400 | 6243266 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6233438 | C | CGCCATTG others(18): Show |
1 | a0003 | 1 | NA19075.hp2 | frameshift_variant&stop_gained | HIGH | c.302_326dupCCATTGAA others(17): Show |
p.Trp109fs | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/8 | 427/1225 | 327/687 | 109/228 | INFO_REALIGN_3_PRIME | chr12 | 6233438 | ||
chr12:6237784 | A | G | 1 | a0002 | 2 | NA18951.hp1 NA18986.hp1 |
missense_variant | MODERATE | c.643A>G | p.Met215Val | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 8/8 | 743/1225 | 643/687 | 215/228 | chr12 | 6237784 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6232684 | G | A | 1 | a0001c0002 | 2 | NA18612.hp2 NA18974.hp2 |
synonymous_variant | LOW | c.228G>A | p.Leu76Leu | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/8 | 328/1225 | 228/687 | 76/228 | chr12 | 6232684 | |||
chr12:6235306 | G | A | 1 | a0001c0005 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.426G>A | p.Thr142Thr | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/8 | 526/1225 | 426/687 | 142/228 | chr12 | 6235306 | |||
chr12:6235559 | C | T | 1 | a0001c0007 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.531C>T | p.Thr177Thr | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/8 | 631/1225 | 531/687 | 177/228 | chr12 | 6235559 | |||
chr12:6236206 | C | T | 1 | a0001c0006 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.552C>T | p.Ala184Ala | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/8 | 652/1225 | 552/687 | 184/228 | chr12 | 6236206 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6200432 | C | T | 1 | a0001c0001t0002 | 48 | HG00733.hp1 HG01346.hp1 HG01358.hp2 others(45): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/8 | chr12 | 6200432 | |||||||
chr12:6238039 | T | G | 1 | a0001c0001t0003 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211T>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 8/8 | 211 | chr12 | 6238039 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6200615 | G | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
5 | HG03017.hp2 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+50G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200615 | |||||||
chr12:6200630 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02055.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.66+65G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200630 | |||||||
chr12:6200729 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
138 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.66+164G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200729 | |||||||
chr12:6200729 | G | C | 9 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
9 | HG02129.hp1 HG02165.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.66+164G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200729 | |||||||
chr12:6200885 | G | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | NA18962.hp1 NA18969.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.66+320G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6200885 | |||||||
chr12:6201007 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.66+442C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201007 | |||||||
chr12:6201044 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0052 others(2): Show |
6 | HG00609.hp2 NA18951.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+479G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201044 | |||||||
chr12:6201091 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0002g0005 a0001c0001t0002g0040 others(12): Show |
21 | HG00733.hp1 HG01516.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.66+526C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201091 | |||||||
chr12:6201103 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
5 | HG02109.hp1 HG02559.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+538C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201103 | |||||||
chr12:6201275 | A | T | 1 | a0001c0001t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.66+710A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201275 | |||||||
chr12:6201306 | C | CA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
143 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.66+742dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6201306 | ||||||
chr12:6201377 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0293 |
3 | HG02559.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.66+812C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201377 | |||||||
chr12:6201455 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.66+890C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201455 | |||||||
chr12:6201477 | G | A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.66+912G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201477 | |||||||
chr12:6201555 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0286 a0001c0001t0001g0288 others(2): Show |
6 | HG02258.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+990C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201555 | |||||||
chr12:6201684 | A | G | 35 | a0001c0001t0001g0005 a0001c0001t0002g0005 a0001c0001t0002g0012 others(32): Show |
46 | HG00733.hp1 HG01346.hp1 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.66+1119A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201684 | |||||||
chr12:6201898 | C | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0283 a0001c0001t0002g0284 others(1): Show |
6 | HG01891.hp1 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+1333C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201898 | |||||||
chr12:6201939 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.66+1374G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201939 | |||||||
chr12:6201994 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
142 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.66+1429C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6201994 | |||||||
chr12:6202066 | A | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0268 a0001c0001t0001g0290 |
5 | HG01192.hp2 HG02055.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+1501A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6202066 | |||||||
chr12:6202404 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.66+1839G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6202404 | |||||||
chr12:6202595 | C | G | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG02717.hp2 HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.66+2030C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6202595 | |||||||
chr12:6202856 | C | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | NA18950.hp1 NA19060.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.66+2291C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6202856 | |||||||
chr12:6203149 | T | C | 35 | a0001c0001t0001g0005 a0001c0001t0002g0005 a0001c0001t0002g0012 others(32): Show |
46 | HG00733.hp1 HG01346.hp1 HG01516.hp2 others(43): Show |
intron_variant | MODIFIER | c.66+2584T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203149 | |||||||
chr12:6203191 | T | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.66+2626T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203191 | |||||||
chr12:6203341 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA18946.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.66+2776G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203341 | |||||||
chr12:6203474 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0159 |
4 | NA18945.hp1 NA18946.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+2909G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203474 | |||||||
chr12:6203497 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
144 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.66+2932G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203497 | |||||||
chr12:6203529 | T | C | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+2964T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203529 | |||||||
chr12:6203945 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.66+3380T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6203945 | |||||||
chr12:6204095 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(57): Show |
76 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.66+3530C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204095 | |||||||
chr12:6204193 | G | T | 14 | a0001c0001t0002g0012 a0001c0001t0002g0036 a0001c0001t0002g0037 others(11): Show |
18 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.66+3628G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204193 | |||||||
chr12:6204233 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0255 others(6): Show |
12 | HG02155.hp2 NA18944.hp1 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+3668A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204233 | |||||||
chr12:6204245 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
222 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.66+3680A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204245 | |||||||
chr12:6204282 | A | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0248 others(6): Show |
11 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.66+3717A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204282 | |||||||
chr12:6204299 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
149 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.66+3734A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204299 | |||||||
chr12:6204407 | A | C | 1 | a0001c0001t0001g0093 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.66+3842A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204407 | |||||||
chr12:6204518 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0149 a0001c0001t0001g0268 |
5 | HG02055.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+3953T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204518 | |||||||
chr12:6204765 | G | A | 26 | a0001c0001t0001g0032 a0001c0001t0001g0094 a0001c0001t0001g0095 others(23): Show |
32 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.66+4200G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204765 | |||||||
chr12:6204879 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
224 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.66+4314C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204879 | |||||||
chr12:6204988 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+4423T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6204988 | |||||||
chr12:6205022 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+4457C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205022 | |||||||
chr12:6205023 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0253 a0001c0001t0001g0254 |
4 | HG02572.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+4458G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205023 | |||||||
chr12:6205077 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
224 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.66+4512T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205077 | |||||||
chr12:6205144 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.66+4579C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205144 | |||||||
chr12:6205160 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+4595T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205160 | |||||||
chr12:6205174 | C | G | 1 | a0001c0001t0002g0281 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.66+4609C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205174 | |||||||
chr12:6205354 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+4789C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205354 | |||||||
chr12:6205501 | G | T | 6 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0163 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+4936G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205501 | |||||||
chr12:6205753 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.66+5188A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205753 | |||||||
chr12:6205788 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.66+5223C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205788 | |||||||
chr12:6205971 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.66+5406G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6205971 | |||||||
chr12:6206013 | C | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0248 others(6): Show |
11 | HG01346.hp1 HG01952.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.66+5448C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206013 | |||||||
chr12:6206158 | C | CA | 18 | a0001c0001t0001g0038 a0001c0001t0001g0055 a0001c0001t0001g0137 others(15): Show |
19 | HG00673.hp2 HG01928.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.66+5608dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206158 | ||||||
chr12:6206158 | CA | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
174 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.66+5608delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206158 | ||||||
chr12:6206158 | CAA | C | 24 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0248 others(21): Show |
30 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.66+5607_66+5608del others(2): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206158 | ||||||
chr12:6206186 | G | C | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+5621G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206186 | |||||||
chr12:6206321 | C | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
147 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.66+5756C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206321 | |||||||
chr12:6206361 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.66+5796T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206361 | |||||||
chr12:6206454 | G | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | NA18969.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.66+5889G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206454 | |||||||
chr12:6206527 | A | C | 1 | a0001c0001t0001g0031 | 2 | HG01934.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.66+5962A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6206527 | |||||||
chr12:6206900 | A | AT | 16 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0134 others(13): Show |
16 | HG00673.hp2 HG01258.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.66+6349dupT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206900 | ||||||
chr12:6206900 | AT | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0176 others(5): Show |
10 | HG02258.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+6349delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6206900 | ||||||
chr12:6207059 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+6494T>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207059 | |||||||
chr12:6207165 | A | C | 6 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0035 others(3): Show |
7 | HG01346.hp1 HG01952.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+6600A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207165 | |||||||
chr12:6207172 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.66+6607A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207172 | |||||||
chr12:6207277 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.66+6712G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207277 | |||||||
chr12:6207295 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0286 a0001c0001t0001g0288 others(1): Show |
5 | HG02258.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+6730C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207295 | |||||||
chr12:6207432 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+6867G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207432 | |||||||
chr12:6207453 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+6888C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207453 | |||||||
chr12:6207494 | A | G | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+6929A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207494 | |||||||
chr12:6207596 | C | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0159 |
4 | NA18945.hp1 NA18946.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+7031C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207596 | |||||||
chr12:6207807 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+7242T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207807 | |||||||
chr12:6207825 | G | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0288 a0001c0001t0003g0287 |
4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+7260G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207825 | |||||||
chr12:6207842 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
157 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.66+7277C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207842 | |||||||
chr12:6207951 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.66+7386G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6207951 | |||||||
chr12:6208020 | T | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0290 a0001c0001t0001g0293 |
4 | HG01192.hp2 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+7455T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208020 | |||||||
chr12:6208148 | T | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0032 others(48): Show |
67 | HG00733.hp1 HG01192.hp2 HG01346.hp1 others(64): Show |
intron_variant | MODIFIER | c.66+7583T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208148 | |||||||
chr12:6208178 | C | G | 9 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+7613C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208178 | |||||||
chr12:6208202 | C | G | 6 | a0001c0001t0001g0251 a0001c0001t0001g0265 a0001c0001t0001g0267 others(3): Show |
6 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+7637C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208202 | |||||||
chr12:6208236 | A | AG | 9 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+7671_66+7672ins others(1): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208236 | |||||||
chr12:6208264 | G | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01074.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.66+7699G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208264 | |||||||
chr12:6208306 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0268 a0001c0001t0001g0286 |
5 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+7741C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208306 | |||||||
chr12:6208419 | A | T | 1 | a0001c0005t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.66+7854A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208419 | |||||||
chr12:6208557 | G | T | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+7992G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208557 | |||||||
chr12:6208575 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+8010G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208575 | |||||||
chr12:6208686 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+8121C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208686 | |||||||
chr12:6208692 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+8127C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208692 | |||||||
chr12:6208730 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.66+8165C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208730 | |||||||
chr12:6208974 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+8409T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6208974 | |||||||
chr12:6209078 | C | G | 1 | a0001c0001t0002g0273 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.66+8513C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209078 | |||||||
chr12:6209374 | A | G | 1 | a0001c0001t0002g0040 | 2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.66+8809A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209374 | |||||||
chr12:6209463 | A | G | 1 | a0001c0001t0002g0273 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.66+8898A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209463 | |||||||
chr12:6209497 | A | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+8932A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209497 | |||||||
chr12:6209599 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.66+9034C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209599 | |||||||
chr12:6209604 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.66+9039C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209604 | |||||||
chr12:6209679 | CT | C | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0045 others(12): Show |
17 | HG01074.hp2 HG01934.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.66+9135delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6209679 | ||||||
chr12:6209679 | CTTTTTTT | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
157 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.66+9129_66+9135del others(7): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6209679 | ||||||
chr12:6209977 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.66+9412G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6209977 | |||||||
chr12:6210022 | T | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+9457T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210022 | |||||||
chr12:6210144 | G | A | 17 | a0001c0001t0001g0250 a0001c0001t0001g0252 a0001c0001t0002g0012 others(14): Show |
21 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.66+9579G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210144 | |||||||
chr12:6210152 | G | GTTC | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
169 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.66+9589_66+9591dup others(3): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6210152 | ||||||
chr12:6210199 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.66+9634C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210199 | |||||||
chr12:6210333 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.66+9768G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210333 | |||||||
chr12:6210361 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.66+9796G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210361 | |||||||
chr12:6210467 | C | G | 21 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0248 others(18): Show |
26 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.66+9902C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210467 | |||||||
chr12:6210473 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66+9908G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210473 | |||||||
chr12:6210578 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0268 a0001c0001t0001g0286 |
5 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+10013C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210578 | |||||||
chr12:6210671 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
158 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.66+10106G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210671 | |||||||
chr12:6210722 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.66+10157A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210722 | |||||||
chr12:6210835 | CT | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0091 a0001c0001t0001g0099 others(15): Show |
19 | HG01074.hp1 HG01255.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.66+10290delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6210835 | ||||||
chr12:6210835 | CTT | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
151 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.66+10289_66+10290d others(4): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6210835 | ||||||
chr12:6210897 | C | T | 5 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | HG00544.hp2 HG00673.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+10332C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210897 | |||||||
chr12:6210917 | A | G | 9 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+10352A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210917 | |||||||
chr12:6210925 | C | A | 10 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0156 others(7): Show |
12 | HG00621.hp1 HG03490.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+10360C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6210925 | |||||||
chr12:6211037 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+10472C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211037 | |||||||
chr12:6211038 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+10473A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211038 | |||||||
chr12:6211043 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+10478G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211043 | |||||||
chr12:6211050 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+10485C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211050 | |||||||
chr12:6211087 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.66+10522T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211087 | |||||||
chr12:6211125 | C | T | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.66+10560C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211125 | |||||||
chr12:6211220 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
171 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.66+10655C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211220 | |||||||
chr12:6211226 | A | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+10661A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211226 | |||||||
chr12:6211232 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0290 a0001c0001t0001g0293 |
4 | HG01192.hp2 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+10667G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211232 | |||||||
chr12:6211558 | G | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02109.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.66+10993G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211558 | |||||||
chr12:6211588 | C | T | 4 | a0001c0001t0001g0251 a0001c0001t0001g0265 a0001c0001t0001g0267 others(1): Show |
4 | HG02615.hp1 HG02723.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+11023C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211588 | |||||||
chr12:6211663 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | NA18962.hp2 NA18992.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+11098C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211663 | |||||||
chr12:6211703 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.66+11138C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211703 | |||||||
chr12:6211895 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.66+11330A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211895 | |||||||
chr12:6211910 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.66+11345C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6211910 | |||||||
chr12:6212415 | A | G | 3 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02109.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.66+11850A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212415 | |||||||
chr12:6212696 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
159 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.66+12131C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212696 | |||||||
chr12:6212826 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.66+12261A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212826 | |||||||
chr12:6212838 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.66+12273A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212838 | |||||||
chr12:6212864 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+12299G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212864 | |||||||
chr12:6212909 | A | G | 7 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0163 others(4): Show |
7 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+12344A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212909 | |||||||
chr12:6212958 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.66+12393G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212958 | |||||||
chr12:6212987 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66+12422G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6212987 | |||||||
chr12:6213028 | C | A | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-12398C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213028 | |||||||
chr12:6213091 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-12335G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213091 | |||||||
chr12:6213119 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.67-12307A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213119 | |||||||
chr12:6213149 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0288 a0001c0001t0003g0287 |
4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-12277T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213149 | |||||||
chr12:6213335 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-12091A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213335 | |||||||
chr12:6213540 | T | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG00408.hp2 HG02132.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.67-11886T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213540 | |||||||
chr12:6213584 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67-11842A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213584 | |||||||
chr12:6213618 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.67-11808C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213618 | |||||||
chr12:6213651 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
240 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.67-11775T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213651 | |||||||
chr12:6213692 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.67-11734T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213692 | |||||||
chr12:6213706 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.67-11720G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213706 | |||||||
chr12:6213788 | A | G | 1 | a0001c0001t0002g0274 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.67-11638A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213788 | |||||||
chr12:6213826 | C | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0229 others(8): Show |
13 | HG03098.hp1 HG03130.hp2 HG03516.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-11600C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213826 | |||||||
chr12:6213828 | A | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0229 others(8): Show |
13 | HG03098.hp1 HG03130.hp2 HG03516.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-11598A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213828 | |||||||
chr12:6213864 | G | T | 1 | a0001c0001t0002g0281 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67-11562G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213864 | |||||||
chr12:6213882 | A | C | 1 | a0001c0001t0001g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.67-11544A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213882 | |||||||
chr12:6213974 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.67-11452G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213974 | |||||||
chr12:6213998 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-11428A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6213998 | |||||||
chr12:6214003 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67-11423A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214003 | |||||||
chr12:6214015 | A | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | NA19085.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.67-11411A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214015 | |||||||
chr12:6214035 | C | A | 21 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0244 others(18): Show |
26 | HG01346.hp1 HG01891.hp1 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.67-11391C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214035 | |||||||
chr12:6214058 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-11368C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214058 | |||||||
chr12:6214134 | T | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
23 | HG00733.hp1 HG01192.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-11292T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214134 | |||||||
chr12:6214227 | C | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(46): Show |
57 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.67-11199C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214227 | |||||||
chr12:6214344 | C | CT | 37 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0039 others(34): Show |
47 | HG00733.hp1 HG01192.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.67-11058dupT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | ||||||
chr12:6214344 | C | CTT | 10 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0229 others(7): Show |
12 | HG02451.hp1 HG03130.hp2 HG03516.hp2 others(9): Show |
intron_variant | MODIFIER | c.67-11059_67-11058d others(4): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | ||||||
chr12:6214344 | C | CTTT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0234 a0001c0001t0001g0254 others(3): Show |
8 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-11060_67-11058d others(5): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | ||||||
chr12:6214344 | C | CTTTT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0103 others(4): Show |
9 | HG02257.hp2 HG02922.hp1 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-11061_67-11058d others(6): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | ||||||
chr12:6214344 | C | CTTTTT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
113 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.67-11062_67-11058d others(7): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | ||||||
chr12:6214344 | C | CTTTTTT | 34 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(31): Show |
37 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.67-11063_67-11058d others(8): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | ||||||
chr12:6214344 | C | CTTTTTTT | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | HG02486.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-11064_67-11058d others(9): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | ||||||
chr12:6214344 | CT | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0186 a0001c0001t0001g0257 others(3): Show |
6 | HG00408.hp2 HG02735.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-11058delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | ||||||
chr12:6214344 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0251 a0001c0001t0001g0265 others(3): Show |
6 | HG02615.hp1 HG02723.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-11066_67-11058d others(11): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6214344 | ||||||
chr12:6214361 | T | C | 3 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02109.hp1 HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67-11065T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214361 | |||||||
chr12:6214439 | T | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | NA18612.hp1 NA18960.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.67-10987T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214439 | |||||||
chr12:6214524 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18968.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.67-10902T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214524 | |||||||
chr12:6214639 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0222 |
2 | HG01081.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.67-10787C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214639 | |||||||
chr12:6214766 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.67-10660G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214766 | |||||||
chr12:6214766 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.67-10660G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6214766 | |||||||
chr12:6215236 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67-10190C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215236 | |||||||
chr12:6215272 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.67-10154A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215272 | |||||||
chr12:6215435 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-9991C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215435 | |||||||
chr12:6215539 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67-9887A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215539 | |||||||
chr12:6215597 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18968.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.67-9829G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215597 | |||||||
chr12:6215709 | A | G | 9 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-9717A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215709 | |||||||
chr12:6215757 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01934.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.67-9669G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215757 | |||||||
chr12:6215805 | C | T | 12 | a0001c0001t0001g0060 a0001c0001t0001g0085 a0001c0001t0001g0087 others(9): Show |
15 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.67-9621C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215805 | |||||||
chr12:6215806 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-9620G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215806 | |||||||
chr12:6215855 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.67-9571C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215855 | |||||||
chr12:6215862 | A | G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0054 others(19): Show |
29 | HG00733.hp1 HG01192.hp2 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.67-9564A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215862 | |||||||
chr12:6215957 | T | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0034 others(11): Show |
18 | HG00558.hp2 NA18944.hp1 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.67-9469T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6215957 | |||||||
chr12:6216256 | C | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-9170C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216256 | |||||||
chr12:6216416 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.67-9010C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216416 | |||||||
chr12:6216497 | C | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-8929C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216497 | |||||||
chr12:6216522 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
23 | HG00733.hp1 HG01192.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-8904T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216522 | |||||||
chr12:6216700 | A | G | 7 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
8 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-8726A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216700 | |||||||
chr12:6216701 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
8 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-8725G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216701 | |||||||
chr12:6216748 | C | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
218 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.67-8678C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216748 | |||||||
chr12:6216909 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67-8517T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216909 | |||||||
chr12:6216918 | A | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-8508A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6216918 | |||||||
chr12:6217078 | T | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-8348T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217078 | |||||||
chr12:6217167 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-8259A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217167 | |||||||
chr12:6217358 | C | CA | 4 | a0001c0001t0001g0038 a0001c0001t0001g0050 a0001c0001t0001g0288 others(1): Show |
5 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-8060dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6217358 | ||||||
chr12:6217461 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0288 a0001c0001t0003g0287 |
4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-7965G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217461 | |||||||
chr12:6217621 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.67-7805A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217621 | |||||||
chr12:6217638 | A | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0288 a0001c0001t0003g0287 |
4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-7788A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217638 | |||||||
chr12:6217734 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67-7692G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217734 | |||||||
chr12:6217842 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
215 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(212): Show |
intron_variant | MODIFIER | c.67-7584A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217842 | |||||||
chr12:6217872 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-7554C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217872 | |||||||
chr12:6217901 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.67-7525A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6217901 | |||||||
chr12:6218001 | G | T | 1 | a0001c0001t0002g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.67-7425G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218001 | |||||||
chr12:6218083 | T | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0290 others(4): Show |
8 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-7343T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218083 | |||||||
chr12:6218087 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.67-7339C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218087 | |||||||
chr12:6218227 | C | CA | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
163 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.67-7187dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6218227 | ||||||
chr12:6218227 | CA | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0159 a0001c0001t0001g0229 others(6): Show |
10 | NA18941.hp1 NA18946.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-7187delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6218227 | ||||||
chr12:6218271 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.67-7155A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218271 | |||||||
chr12:6218299 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67-7127G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218299 | |||||||
chr12:6218605 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.67-6821C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218605 | |||||||
chr12:6218651 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.67-6775A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218651 | |||||||
chr12:6218752 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0127 |
4 | NA18939.hp1 NA18990.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-6674G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218752 | |||||||
chr12:6218754 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.67-6672G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218754 | |||||||
chr12:6218823 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
216 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.67-6603T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218823 | |||||||
chr12:6218841 | G | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0290 a0001c0001t0001g0293 |
4 | HG01192.hp2 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-6585G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218841 | |||||||
chr12:6218892 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.67-6534C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218892 | |||||||
chr12:6218947 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0101 a0001c0001t0002g0005 others(5): Show |
14 | HG00733.hp1 HG01891.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-6479T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6218947 | |||||||
chr12:6219154 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
180 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.67-6272C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219154 | |||||||
chr12:6219163 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.67-6263G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219163 | |||||||
chr12:6219166 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0002g0294 |
2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.67-6260C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219166 | |||||||
chr12:6219524 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA18946.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.67-5902C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219524 | |||||||
chr12:6219540 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.67-5886C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219540 | |||||||
chr12:6219564 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | NA18956.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.67-5862C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219564 | |||||||
chr12:6219631 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.67-5795A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219631 | |||||||
chr12:6219635 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.67-5791G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219635 | |||||||
chr12:6219977 | A | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0047 others(12): Show |
22 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-5449A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6219977 | |||||||
chr12:6220082 | G | A | 12 | a0001c0001t0001g0060 a0001c0001t0001g0085 a0001c0001t0001g0087 others(9): Show |
15 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.67-5344G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220082 | |||||||
chr12:6220125 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.67-5301T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220125 | |||||||
chr12:6220446 | G | T | 1 | a0001c0001t0002g0152 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-4980G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220446 | |||||||
chr12:6220450 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-4976T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220450 | |||||||
chr12:6220466 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-4960G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220466 | |||||||
chr12:6220568 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.67-4858G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220568 | |||||||
chr12:6220629 | T | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0290 others(4): Show |
8 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-4797T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220629 | |||||||
chr12:6220758 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.67-4668A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220758 | |||||||
chr12:6220845 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.67-4581C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6220845 | |||||||
chr12:6221204 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG00438.hp1 HG00621.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.67-4222C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221204 | |||||||
chr12:6221306 | G | A | 21 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0034 others(18): Show |
25 | HG00558.hp2 HG03017.hp1 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.67-4120G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221306 | |||||||
chr12:6221434 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-3992G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221434 | |||||||
chr12:6221446 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-3980C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221446 | |||||||
chr12:6221526 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.67-3900A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221526 | |||||||
chr12:6221556 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG00408.hp2 HG02132.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.67-3870G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221556 | |||||||
chr12:6221813 | C | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0198 a0001c0001t0001g0214 others(1): Show |
7 | HG00733.hp2 HG01175.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-3613C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221813 | |||||||
chr12:6221813 | C | CA | 19 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0087 others(16): Show |
19 | HG00621.hp2 HG01358.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.67-3593dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6221813 | ||||||
chr12:6221813 | CA | C | 41 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(38): Show |
46 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.67-3593delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6221813 | ||||||
chr12:6221861 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-3565G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221861 | |||||||
chr12:6221878 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-3548C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221878 | |||||||
chr12:6221926 | C | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0197 a0001c0001t0001g0199 others(2): Show |
6 | HG00609.hp1 HG01255.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-3500C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6221926 | |||||||
chr12:6222042 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG00735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.67-3384C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222042 | |||||||
chr12:6222085 | T | G | 1 | a0001c0001t0002g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-3341T>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222085 | |||||||
chr12:6222103 | C | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0113 others(2): Show |
5 | NA18939.hp2 NA18982.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-3323C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222103 | |||||||
chr12:6222262 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.67-3164G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222262 | |||||||
chr12:6222321 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG01934.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.67-3105C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222321 | |||||||
chr12:6222323 | A | T | 1 | a0001c0001t0001g0029 | 2 | HG01934.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.67-3103A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222323 | |||||||
chr12:6222355 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.67-3071T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222355 | |||||||
chr12:6222415 | C | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-3011C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222415 | |||||||
chr12:6222428 | A | G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0163 others(5): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-2998A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222428 | |||||||
chr12:6222506 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67-2920G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222506 | |||||||
chr12:6222525 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-2901G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222525 | |||||||
chr12:6222584 | AAG | A | 8 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0163 others(5): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-2838_67-2837del others(2): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6222584 | ||||||
chr12:6222724 | A | C | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-2702A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222724 | |||||||
chr12:6222778 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67-2648T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6222778 | |||||||
chr12:6223017 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67-2409A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223017 | |||||||
chr12:6223032 | C | G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0163 others(5): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-2394C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223032 | |||||||
chr12:6223144 | G | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(127): Show |
157 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.67-2282G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223144 | |||||||
chr12:6223261 | CT | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(174): Show |
213 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(210): Show |
intron_variant | MODIFIER | c.67-2147delT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6223261 | ||||||
chr12:6223354 | C | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.67-2072C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223354 | |||||||
chr12:6223409 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0256 |
2 | HG02155.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67-2017C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223409 | |||||||
chr12:6223564 | C | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.67-1862C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223564 | |||||||
chr12:6223590 | TG | T | 18 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): Show |
21 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.67-1828delG | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 6223590 | ||||||
chr12:6223596 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0290 a0001c0001t0001g0293 |
4 | HG01192.hp2 HG02559.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-1830G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223596 | |||||||
chr12:6223597 | G | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0257 others(4): Show |
10 | NA18944.hp1 NA18959.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-1829G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223597 | |||||||
chr12:6223598 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0002g0035 a0001c0001t0002g0270 others(2): Show |
6 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-1828G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223598 | |||||||
chr12:6223660 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.67-1766C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223660 | |||||||
chr12:6223672 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
295 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(292): Show |
intron_variant | MODIFIER | c.67-1754A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223672 | |||||||
chr12:6223721 | G | A | 18 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): Show |
21 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.67-1705G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223721 | |||||||
chr12:6223744 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(137): Show |
169 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.67-1682A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223744 | |||||||
chr12:6223760 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.67-1666G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223760 | |||||||
chr12:6223778 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-1648C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223778 | |||||||
chr12:6223870 | C | G | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-1556C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6223870 | |||||||
chr12:6224014 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67-1412G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224014 | |||||||
chr12:6224039 | C | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0044 others(17): Show |
25 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.67-1387C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224039 | |||||||
chr12:6224353 | A | T | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67-1073A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224353 | |||||||
chr12:6224418 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67-1008A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224418 | |||||||
chr12:6224422 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67-1004C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224422 | |||||||
chr12:6224442 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.67-984A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224442 | |||||||
chr12:6224546 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0002g0301 a0001c0007t0001g0162 |
3 | HG02976.hp2 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.67-880G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224546 | |||||||
chr12:6224562 | G | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-864G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224562 | |||||||
chr12:6224705 | C | T | 8 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0163 others(5): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-721C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224705 | |||||||
chr12:6224724 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.67-702C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224724 | |||||||
chr12:6224729 | G | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.67-697G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224729 | |||||||
chr12:6224759 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.67-667T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224759 | |||||||
chr12:6224808 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.67-618A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6224808 | |||||||
chr12:6225019 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.67-407C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225019 | |||||||
chr12:6225208 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.67-218C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225208 | |||||||
chr12:6225247 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0254 |
3 | HG03098.hp1 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.67-179T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225247 | |||||||
chr12:6225322 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.67-104C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225322 | |||||||
chr12:6225363 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.67-63C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 1/7 | chr12 | 6225363 | |||||||
chr12:6225563 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.175+29C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6225563 | |||||||
chr12:6225563 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.175+29C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6225563 | |||||||
chr12:6225706 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.175+172G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6225706 | |||||||
chr12:6225719 | C | T | 3 | a0001c0001t0001g0267 a0001c0001t0002g0301 a0001c0007t0001g0162 |
3 | HG02976.hp2 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.175+185C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6225719 | |||||||
chr12:6226312 | G | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+778G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226312 | |||||||
chr12:6226384 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0001g0122 others(2): Show |
6 | NA18957.hp1 NA18968.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+850G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226384 | |||||||
chr12:6226581 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.175+1047G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226581 | |||||||
chr12:6226633 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+1099G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226633 | |||||||
chr12:6226733 | A | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0278 |
3 | HG02886.hp2 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.175+1199A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226733 | |||||||
chr12:6226741 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+1207A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226741 | |||||||
chr12:6226818 | A | G | 16 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+1284A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226818 | |||||||
chr12:6226872 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.175+1338G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226872 | |||||||
chr12:6226971 | C | G | 1 | a0001c0001t0002g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.175+1437C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226971 | |||||||
chr12:6226978 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.175+1444A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6226978 | |||||||
chr12:6227019 | T | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.175+1485T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227019 | |||||||
chr12:6227053 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0047 others(20): Show |
30 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.175+1519T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227053 | |||||||
chr12:6227138 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.175+1604A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227138 | |||||||
chr12:6227181 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.175+1647A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227181 | |||||||
chr12:6227195 | T | TTTTTTTT others(331): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1661_175+1662i others(340): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227195 | |||||||
chr12:6227196 | A | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1662A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227196 | |||||||
chr12:6227205 | A | AT | 16 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+1681dupT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6227205 | ||||||
chr12:6227377 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+1843T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227377 | |||||||
chr12:6227386 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.175+1852C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227386 | |||||||
chr12:6227639 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.175+2105C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227639 | |||||||
chr12:6227707 | G | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18963.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.175+2173G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227707 | |||||||
chr12:6227846 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.175+2312G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227846 | |||||||
chr12:6227875 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0198 a0001c0001t0001g0214 |
6 | HG00733.hp2 HG01175.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+2341C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227875 | |||||||
chr12:6227910 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0053 a0001c0001t0001g0116 others(1): Show |
5 | HG01346.hp2 HG02004.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+2376G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6227910 | |||||||
chr12:6228014 | G | C | 16 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+2480G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228014 | |||||||
chr12:6228017 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.175+2483G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228017 | |||||||
chr12:6228088 | G | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(128): Show |
159 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.175+2554G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228088 | |||||||
chr12:6228121 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0288 a0001c0001t0003g0287 |
4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+2587G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228121 | |||||||
chr12:6228132 | T | A | 1 | a0001c0001t0002g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.175+2598T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228132 | |||||||
chr12:6228163 | G | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+2629G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228163 | |||||||
chr12:6228183 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.175+2649C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228183 | |||||||
chr12:6228228 | A | G | 16 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+2694A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228228 | |||||||
chr12:6228265 | A | C | 16 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.175+2731A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228265 | |||||||
chr12:6228336 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0047 others(12): Show |
22 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.175+2802G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228336 | |||||||
chr12:6228558 | C | CA | 22 | a0001c0001t0001g0050 a0001c0001t0001g0077 a0001c0001t0001g0079 others(19): Show |
22 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.175+3047dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6228558 | ||||||
chr12:6228558 | CA | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
180 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.175+3047delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6228558 | ||||||
chr12:6228558 | CAA | C | 24 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0044 others(21): Show |
29 | HG01346.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.175+3046_175+3047d others(4): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6228558 | ||||||
chr12:6228558 | CAAA | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0286 a0001c0001t0001g0289 others(3): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+3045_175+3047d others(5): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6228558 | ||||||
chr12:6228576 | A | C | 3 | a0001c0001t0001g0267 a0001c0001t0002g0301 a0001c0007t0001g0162 |
3 | HG02976.hp2 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.175+3042A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228576 | |||||||
chr12:6228655 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.175+3121A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228655 | |||||||
chr12:6228690 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.175+3156G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228690 | |||||||
chr12:6228709 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0163 a0001c0001t0002g0294 |
3 | HG01884.hp1 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.175+3175C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228709 | |||||||
chr12:6228743 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+3209C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228743 | |||||||
chr12:6228758 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0288 a0001c0001t0003g0287 |
4 | HG02451.hp2 HG02615.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+3224C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228758 | |||||||
chr12:6228773 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.175+3239G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228773 | |||||||
chr12:6228808 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(168): Show |
207 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.175+3274A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6228808 | |||||||
chr12:6229252 | C | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
14 | HG01109.hp1 HG01358.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.176-3380C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229252 | |||||||
chr12:6229460 | A | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-3172A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229460 | |||||||
chr12:6229471 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(169): Show |
207 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.176-3161C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229471 | |||||||
chr12:6229492 | T | C | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.176-3140T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229492 | |||||||
chr12:6229500 | C | G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0054 a0001c0001t0001g0163 others(5): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-3132C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229500 | |||||||
chr12:6229546 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-3086C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229546 | |||||||
chr12:6229679 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-2953A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229679 | |||||||
chr12:6229711 | G | GTCC | 14 | a0001c0001t0001g0060 a0001c0001t0001g0085 a0001c0001t0001g0087 others(11): Show |
17 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.176-2918_176-2916d others(5): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6229711 | ||||||
chr12:6229724 | G | C | 16 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-2908G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229724 | |||||||
chr12:6229779 | A | G | 4 | a0001c0001t0001g0148 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | NA18962.hp2 NA18970.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-2853A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229779 | |||||||
chr12:6229820 | C | CT | 5 | a0001c0001t0001g0029 a0001c0001t0001g0050 a0001c0001t0001g0097 others(2): Show |
6 | HG01934.hp2 HG02698.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-2796dupT | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 6229820 | ||||||
chr12:6229963 | G | A | 16 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0054 others(13): Show |
18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.176-2669G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6229963 | |||||||
chr12:6230245 | G | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
7 | NA18967.hp2 NA18969.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-2387G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230245 | |||||||
chr12:6230282 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0176 |
3 | NA18747.hp2 NA19074.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.176-2350G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230282 | |||||||
chr12:6230420 | C | T | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-2212C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230420 | |||||||
chr12:6230422 | T | G | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-2210T>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230422 | |||||||
chr12:6230447 | C | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0229 |
3 | NA18999.hp1 NA19088.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.176-2185C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230447 | |||||||
chr12:6230491 | G | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-2141G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230491 | |||||||
chr12:6230555 | T | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-2077T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230555 | |||||||
chr12:6230690 | T | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(174): Show |
213 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(210): Show |
intron_variant | MODIFIER | c.176-1942T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230690 | |||||||
chr12:6230697 | A | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
335 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(332): Show |
intron_variant | MODIFIER | c.176-1935A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230697 | |||||||
chr12:6230743 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.176-1889G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230743 | |||||||
chr12:6230803 | C | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-1829C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230803 | |||||||
chr12:6230804 | A | G | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-1828A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230804 | |||||||
chr12:6230873 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.176-1759G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6230873 | |||||||
chr12:6231072 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-1560G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231072 | |||||||
chr12:6231073 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-1559T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231073 | |||||||
chr12:6231079 | TGTGTATT others(9): Show |
T | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-1552_176-1537d others(18): Show |
CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231079 | |||||||
chr12:6231121 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-1511C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231121 | |||||||
chr12:6231169 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.176-1463G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231169 | |||||||
chr12:6231222 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(125): Show |
155 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.176-1410T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231222 | |||||||
chr12:6231230 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.176-1402C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231230 | |||||||
chr12:6231276 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.176-1356A>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231276 | |||||||
chr12:6231345 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.176-1287C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231345 | |||||||
chr12:6231397 | A | T | 1 | a0001c0001t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.176-1235A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231397 | |||||||
chr12:6231901 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.176-731T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231901 | |||||||
chr12:6231966 | C | A | 1 | a0003c0004t0001g0146 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.176-666C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6231966 | |||||||
chr12:6232032 | C | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-600C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232032 | |||||||
chr12:6232050 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.176-582T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232050 | |||||||
chr12:6232327 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.176-305A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232327 | |||||||
chr12:6232333 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(158): Show |
194 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(191): Show |
intron_variant | MODIFIER | c.176-299G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232333 | |||||||
chr12:6232336 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.176-296G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232336 | |||||||
chr12:6232394 | G | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0210 |
2 | HG00621.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.176-238G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232394 | |||||||
chr12:6232602 | C | T | 5 | a0001c0001t0001g0137 a0001c0001t0001g0267 a0001c0001t0002g0152 others(2): Show |
5 | HG02976.hp2 HG03130.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-30C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 2/7 | chr12 | 6232602 | |||||||
chr12:6232899 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0209 |
2 | HG02132.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.273+170C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6232899 | |||||||
chr12:6232902 | T | C | 1 | a0001c0001t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+173T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6232902 | |||||||
chr12:6233075 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0163 a0001c0001t0002g0281 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-337G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6233075 | |||||||
chr12:6233111 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-301A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6233111 | |||||||
chr12:6233391 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.274-21C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 3/7 | chr12 | 6233391 | |||||||
chr12:6233614 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.348+128C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233614 | |||||||
chr12:6233755 | G | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(118): Show |
148 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.348+269G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233755 | |||||||
chr12:6233841 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.348+355C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233841 | |||||||
chr12:6233890 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.348+404C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233890 | |||||||
chr12:6233909 | C | G | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG02155.hp2 HG02165.hp2 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.348+423C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233909 | |||||||
chr12:6233957 | C | T | 26 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0044 others(23): Show |
30 | HG00609.hp1 HG01255.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.348+471C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233957 | |||||||
chr12:6233985 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0003g0287 |
2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.348+499A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6233985 | |||||||
chr12:6234258 | G | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0104 a0001c0001t0001g0113 |
3 | NA18952.hp1 NA18981.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.348+772G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234258 | |||||||
chr12:6234284 | G | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
2 | HG01358.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.348+798G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234284 | |||||||
chr12:6234414 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.349-815G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234414 | |||||||
chr12:6234470 | T | TA | 21 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0023 others(18): Show |
25 | HG00621.hp1 HG01358.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.349-743dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 6234470 | ||||||
chr12:6234470 | TA | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0050 others(27): Show |
36 | HG00423.hp2 HG00733.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.349-743delA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 6234470 | ||||||
chr12:6234489 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.349-740T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234489 | |||||||
chr12:6234648 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.349-581G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234648 | |||||||
chr12:6234684 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.349-545C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6234684 | |||||||
chr12:6235008 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
239 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(236): Show |
intron_variant | MODIFIER | c.349-221A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235008 | |||||||
chr12:6235013 | G | A | 9 | a0001c0001t0001g0039 a0001c0001t0001g0267 a0001c0001t0001g0290 others(6): Show |
11 | HG01192.hp2 HG01884.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-216G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235013 | |||||||
chr12:6235038 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.349-191G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235038 | |||||||
chr12:6235186 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349-43G>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235186 | |||||||
chr12:6235203 | G | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0001g0076 others(2): Show |
5 | HG00735.hp1 HG01928.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-26G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235203 | |||||||
chr12:6235209 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.349-20C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235209 | |||||||
chr12:6235220 | C | G | 2 | a0001c0001t0001g0288 a0001c0001t0003g0287 |
2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.349-9C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 4/7 | chr12 | 6235220 | |||||||
chr12:6235335 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0002g0272 |
4 | HG02451.hp1 NA18959.hp2 NA18983.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.447+8G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235335 | |||||||
chr12:6235361 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.447+34T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235361 | |||||||
chr12:6235434 | C | A | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(167): Show |
205 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(202): Show |
intron_variant | MODIFIER | c.448-42C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235434 | |||||||
chr12:6235437 | T | A | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.448-39T>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235437 | |||||||
chr12:6235454 | C | A | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.448-22C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235454 | |||||||
chr12:6235455 | A | T | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.448-21A>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235455 | |||||||
chr12:6235456 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.448-20T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 5/7 | chr12 | 6235456 | |||||||
chr12:6235659 | C | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0229 others(11): Show |
16 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.537+94C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/7 | chr12 | 6235659 | |||||||
chr12:6235914 | G | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
211 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.538-278G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/7 | chr12 | 6235914 | |||||||
chr12:6235977 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0286 a0001c0001t0001g0288 others(1): Show |
6 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-215A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/7 | chr12 | 6235977 | |||||||
chr12:6236033 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
176 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.538-159C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 6/7 | chr12 | 6236033 | |||||||
chr12:6236292 | C | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0205 a0001c0001t0001g0229 others(6): Show |
10 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+17C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236292 | |||||||
chr12:6236365 | C | G | 1 | a0001c0001t0002g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.621+90C>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236365 | |||||||
chr12:6236440 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.621+165C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236440 | |||||||
chr12:6236577 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.621+302A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236577 | |||||||
chr12:6236578 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+303T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236578 | |||||||
chr12:6236590 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+315C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236590 | |||||||
chr12:6236618 | C | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(126): Show |
159 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.621+343C>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236618 | |||||||
chr12:6236783 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.621+508C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236783 | |||||||
chr12:6236807 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0047 others(26): Show |
36 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.621+532G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236807 | |||||||
chr12:6236826 | TC | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+556delC | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 6236826 | ||||||
chr12:6236906 | C | T | 5 | a0001c0001t0001g0244 a0001c0001t0001g0288 a0001c0001t0002g0275 others(2): Show |
5 | HG02258.hp1 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+631C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236906 | |||||||
chr12:6236926 | A | G | 15 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
18 | HG01346.hp1 HG01952.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.621+651A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236926 | |||||||
chr12:6236949 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18941.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.621+674G>A | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6236949 | |||||||
chr12:6237221 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(168): Show |
208 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.622-542T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237221 | |||||||
chr12:6237263 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.622-500C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237263 | |||||||
chr12:6237289 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.622-474C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237289 | |||||||
chr12:6237312 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(171): Show |
211 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.622-451T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237312 | |||||||
chr12:6237314 | T | C | 9 | a0001c0001t0001g0039 a0001c0001t0001g0267 a0001c0001t0001g0290 others(6): Show |
11 | HG01192.hp2 HG01884.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.622-449T>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237314 | |||||||
chr12:6237387 | G | GA | 6 | a0001c0001t0001g0031 a0001c0001t0001g0197 a0001c0001t0001g0199 others(3): Show |
7 | HG00609.hp1 HG01255.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-366dupA | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 6237387 | ||||||
chr12:6237505 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622-258A>G | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237505 | |||||||
chr12:6237635 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | NA18941.hp1 NA18967.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-128C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237635 | |||||||
chr12:6237700 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0286 |
4 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-63C>T | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237700 | |||||||
chr12:6237721 | G | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0163 a0001c0001t0002g0294 |
3 | HG01884.hp1 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.622-42G>C | CD9 | ENSG00000010278.15 | transcript | ENST00000009180.10 | protein_coding | 7/7 | chr12 | 6237721 |