Item | Value |
---|---|
geneid | 1431 |
ensemblid | ENSG00000062485.19 |
hgncid | 2422 |
symbol | CS |
name | citrate synthase |
refseq_nuc | NM_004077.3 |
refseq_prot | NP_004068.2 |
ensembl_nuc | ENST00000351328.8 |
ensembl_prot | ENSP00000342056.3 |
mane_status | MANE Select |
chr | chr12 |
start | 56271699 |
end | 56300330 |
strand | - |
ver | v1.2 |
region | chr12:56271699-56300330 |
region5000 | chr12:56266699-56305330 |
regionname0 | CS_chr12_56271699_56300330 |
regionname5000 | CS_chr12_56266699_56305330 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 466 | 314 | 80 | 69 | 121 | 14 | 28 | 87 | CS_chr12_56266699_56305330 | CS | MALLT others(461): Show |
chr12 | 56266699 | 56305330 |
a0002 | 0/0 | 95 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | MALLT others(90): Show |
chr12 | 56266699 | 56305330 |
a0003 | 0/0 | 466 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | MALLT others(461): Show |
chr12 | 56266699 | 56305330 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1398 | 294 | 78 | 65 | 109 | 12 | 28 | CS_chr12_56266699_56305330 | CS | ATGGC others(1393): Show |
chr12 | 56266699 | 56305330 | ||
a0001c0002 | 0/0 | 1398 | 18 | 0 | 4 | 12 | 2 | 0 | CS_chr12_56266699_56305330 | CS | ATGGC others(1393): Show |
chr12 | 56266699 | 56305330 | ||
a0001c0003 | 0/0 | 1398 | 2 | 2 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | ATGGC others(1393): Show |
chr12 | 56266699 | 56305330 | ||
a0002c0004 | 0/0 | 1447 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | ATGGC others(1442): Show |
chr12 | 56266699 | 56305330 | ||
a0003c0005 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | ATGGC others(1393): Show |
chr12 | 56266699 | 56305330 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2915 | 273 | 66 | 61 | 105 | 12 | 27 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0003 | 0/0 | 2915 | 6 | 4 | 2 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0004 | 0/0 | 2915 | 4 | 0 | 0 | 4 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0005 | 0/0 | 2915 | 3 | 3 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0006 | 0/0 | 2915 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0007 | 0/0 | 2915 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0008 | 0/0 | 2915 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0009 | 0/0 | 2915 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0010 | 0/0 | 2915 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0011 | 0/0 | 2915 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0012 | 0/0 | 2915 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0001t0013 | 0/0 | 2915 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0001c0002t0002 | 0/0 | 2914 | 18 | 0 | 4 | 12 | 2 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2909): Show |
chr12 | 56266699 | 56305330 |
a0001c0003t0001 | 0/0 | 2915 | 2 | 2 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
a0002c0004t0001 | 0/0 | 2964 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2959): Show |
chr12 | 56266699 | 56305330 |
a0003c0005t0001 | 0/0 | 2915 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | CCTTC others(2910): Show |
chr12 | 56266699 | 56305330 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 2 | 4 | 5 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 2 | 4 | 1 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0010g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0011g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0012g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0001t0013g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0002c0004t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
a0003c0005t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | FIN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00741 | hp1 | a0001 | c0001 | t0013 | g0072 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0254 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01358 | hp2 | a0001 | c0001 | t0012 | g0227 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0022 | EUR | IBS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0260 | EUR | IBS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01928 | hp1 | a0002 | c0004 | t0001 | g0201 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0114 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0258 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0108 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03239 | hp1 | a0001 | c0001 | t0011 | g0042 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18982 | hp1 | a0003 | c0005 | t0001 | g0196 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19072 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0191 | AFR | ASW | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | GIH | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | MSL | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0173 | AFR | USA | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0143 | REF | REF | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0111 | REF | REF | CS_chr12_56266699_56305330 | CS | chr12 | 56266699 | 56305330 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:56282430 | T | G | 1 | a0003 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.578A>C | p.Lys193Thr | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/11 | 707/2915 | 578/1401 | 193/466 | chr12 | 56282430 | |||
chr12:56282972 | A | AAGCCTCG others(42): Show |
1 | a0002 | 1 | HG01928.hp1 | frameshift_variant&stop_gained | HIGH | c.268-30_286dupGAGTT others(44): Show |
p.Phe96fs | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 5/11 | 415/2915 | 286/1401 | 96/466 | chr12 | 56282972 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:56276015 | G | A | 1 | a0001c0003 | 2 | HG02280.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.769C>T | p.Leu257Leu | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 7/11 | 898/2915 | 769/1401 | 257/466 | chr12 | 56276015 | |||
chr12:56285967 | A | G | 1 | a0001c0002 | 18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
synonymous_variant | LOW | c.150T>C | p.Thr50Thr | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/11 | 279/2915 | 150/1401 | 50/466 | chr12 | 56285967 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:56271948 | T | G | 1 | a0001c0001t0009 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1136A>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 1136 | chr12 | 56271948 | ||||||
chr12:56271996 | G | A | 1 | a0001c0001t0010 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1088C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 1088 | chr12 | 56271996 | ||||||
chr12:56272076 | C | A | 1 | a0001c0001t0005 | 3 | HG02572.hp2 HG02647.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1008G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 1008 | chr12 | 56272076 | ||||||
chr12:56272363 | G | A | 1 | a0001c0001t0011 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*721C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 721 | chr12 | 56272363 | ||||||
chr12:56272439 | C | T | 1 | a0001c0001t0008 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*645G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 645 | chr12 | 56272439 | ||||||
chr12:56272477 | T | A | 1 | a0001c0001t0012 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607A>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 607 | chr12 | 56272477 | ||||||
chr12:56272477 | TA | T | 1 | a0001c0002t0002 | 18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*606delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 606 | chr12 | 56272477 | ||||||
chr12:56272730 | G | A | 1 | a0001c0001t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 354 | chr12 | 56272730 | ||||||
chr12:56272748 | C | T | 1 | a0001c0001t0007 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 336 | chr12 | 56272748 | ||||||
chr12:56272752 | C | T | 1 | a0001c0001t0006 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*332G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 332 | chr12 | 56272752 | ||||||
chr12:56272805 | G | T | 1 | a0001c0001t0004 | 4 | NA18948.hp1 NA19000.hp2 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*279C>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 11/11 | 279 | chr12 | 56272805 | ||||||
chr12:56300215 | C | T | 2 | a0001c0001t0003 a0001c0001t0006 |
7 | HG01167.hp1 HG01169.hp1 HG02630.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/11 | 14 | chr12 | 56300215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:56273316 | A | G | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1231-62T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 10/10 | chr12 | 56273316 | |||||||
chr12:56273475 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1230+112A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 10/10 | chr12 | 56273475 | |||||||
chr12:56273514 | T | C | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1230+73A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 10/10 | chr12 | 56273514 | |||||||
chr12:56273820 | T | C | 17 | a0001c0001t0001g0141 a0001c0001t0001g0183 a0001c0002t0002g0020 others(14): Show |
20 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.1021-24A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56273820 | |||||||
chr12:56273997 | C | CT | 58 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
74 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.1021-202dupA | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56273997 | |||||||
chr12:56273997 | CTT | C | 15 | a0001c0001t0001g0154 a0001c0002t0002g0020 a0001c0002t0002g0021 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1021-203_1021-202d others(4): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56273997 | |||||||
chr12:56274101 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1021-305C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56274101 | |||||||
chr12:56274110 | C | T | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1021-314G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56274110 | |||||||
chr12:56274211 | C | A | 1 | a0001c0001t0001g0213 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1021-415G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56274211 | |||||||
chr12:56274320 | T | TA | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
223 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1020+456dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56274320 | |||||||
chr12:56274320 | T | TAA | 10 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0055 others(7): Show |
10 | HG01175.hp2 HG02056.hp2 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+455_1020+456d others(4): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56274320 | |||||||
chr12:56274390 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
75 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.1020+387T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56274390 | |||||||
chr12:56274596 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0054 |
3 | NA18942.hp1 NA18982.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1020+181A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56274596 | |||||||
chr12:56274640 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1020+137A>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 9/10 | chr12 | 56274640 | |||||||
chr12:56275278 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.789-147T>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 7/10 | chr12 | 56275278 | |||||||
chr12:56275313 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.789-182C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 7/10 | chr12 | 56275313 | |||||||
chr12:56275402 | G | A | 1 | a0001c0001t0003g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.789-271C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 7/10 | chr12 | 56275402 | |||||||
chr12:56275569 | T | TA | 10 | a0001c0001t0001g0106 a0001c0001t0001g0122 a0001c0001t0001g0139 others(7): Show |
10 | HG01070.hp1 HG01175.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.788+426dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 7/10 | chr12 | 56275569 | |||||||
chr12:56275589 | A | AT | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.788+406_788+407ins others(1): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 7/10 | chr12 | 56275589 | |||||||
chr12:56275589 | A | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0049 others(6): Show |
9 | HG01168.hp2 HG01516.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.788+407T>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 7/10 | chr12 | 56275589 | |||||||
chr12:56275805 | C | G | 2 | a0001c0002t0002g0256 a0001c0002t0002g0258 |
2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.788+191G>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 7/10 | chr12 | 56275805 | |||||||
chr12:56276487 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.589-292T>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56276487 | |||||||
chr12:56276641 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.589-446T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56276641 | |||||||
chr12:56276834 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.589-639C>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56276834 | |||||||
chr12:56277202 | TA | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.589-1008delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56277202 | |||||||
chr12:56277363 | G | A | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.589-1168C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56277363 | |||||||
chr12:56277391 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.589-1196G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56277391 | |||||||
chr12:56277426 | C | G | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.589-1231G>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56277426 | |||||||
chr12:56277505 | TA | T | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.589-1311delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56277505 | |||||||
chr12:56277630 | C | CT | 6 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0145 others(3): Show |
6 | HG01255.hp1 HG01928.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-1436dupA | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56277630 | |||||||
chr12:56277684 | A | C | 1 | a0001c0001t0001g0040 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.589-1489T>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56277684 | |||||||
chr12:56277732 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0089 |
2 | NA18950.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.589-1537C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56277732 | |||||||
chr12:56277926 | G | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0217 |
2 | HG02071.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.589-1731C>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56277926 | |||||||
chr12:56278104 | G | T | 6 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-1909C>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278104 | |||||||
chr12:56278322 | T | A | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.589-2127A>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278322 | |||||||
chr12:56278408 | G | A | 1 | a0001c0001t0013g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.589-2213C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278408 | |||||||
chr12:56278505 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.589-2310C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278505 | |||||||
chr12:56278511 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.589-2316G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278511 | |||||||
chr12:56278514 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.589-2319C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278514 | |||||||
chr12:56278635 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0222 |
2 | NA18960.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.589-2440C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278635 | |||||||
chr12:56278734 | GA | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0141 a0001c0001t0001g0161 others(5): Show |
8 | HG00423.hp2 HG01069.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.589-2540delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278734 | |||||||
chr12:56278881 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589-2686G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278881 | |||||||
chr12:56278918 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.589-2723A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278918 | |||||||
chr12:56278964 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.589-2769C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278964 | |||||||
chr12:56278971 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0164 |
2 | HG01261.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.589-2776G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56278971 | |||||||
chr12:56279481 | A | G | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG02145.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2939T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279481 | |||||||
chr12:56279493 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.588+2927C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279493 | |||||||
chr12:56279548 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.588+2872G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279548 | |||||||
chr12:56279633 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.588+2787C>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279633 | |||||||
chr12:56279652 | A | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0125 a0001c0001t0001g0130 others(6): Show |
10 | HG01891.hp2 HG02145.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.588+2768T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279652 | |||||||
chr12:56279694 | A | C | 1 | a0001c0002t0002g0258 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.588+2726T>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279694 | |||||||
chr12:56279765 | C | CA | 9 | a0001c0001t0001g0039 a0001c0001t0001g0091 a0001c0001t0001g0095 others(6): Show |
9 | HG01433.hp1 HG01928.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+2654dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279765 | |||||||
chr12:56279777 | C | CA | 25 | a0001c0001t0001g0096 a0001c0001t0001g0128 a0001c0001t0001g0242 others(22): Show |
28 | HG00642.hp1 HG01106.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.588+2642dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279777 | |||||||
chr12:56279797 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.588+2623C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279797 | |||||||
chr12:56279850 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.588+2570G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279850 | |||||||
chr12:56279927 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.588+2493G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56279927 | |||||||
chr12:56280414 | C | CAA | 4 | a0001c0001t0001g0033 a0001c0001t0001g0068 a0001c0001t0001g0155 others(1): Show |
4 | HG02132.hp1 HG02280.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2005_588+2006i others(4): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280414 | |||||||
chr12:56280414 | C | CAAA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
113 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.588+2005_588+2006i others(5): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280414 | |||||||
chr12:56280414 | C | CAAAA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(26): Show |
31 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.588+2005_588+2006i others(6): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280414 | |||||||
chr12:56280414 | C | CAAAAA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(5): Show |
9 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.588+2005_588+2006i others(7): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280414 | |||||||
chr12:56280415 | C | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.588+2005G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280415 | |||||||
chr12:56280415 | C | CA | 8 | a0001c0001t0001g0019 a0001c0001t0001g0125 a0001c0001t0001g0128 others(5): Show |
9 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+2004_588+2005i others(3): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280415 | |||||||
chr12:56280415 | C | CAA | 3 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0165 |
3 | HG02145.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.588+2004_588+2005i others(4): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280415 | |||||||
chr12:56280416 | C | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.588+2004G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280416 | |||||||
chr12:56280416 | C | CA | 9 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0117 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.588+2003dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280416 | |||||||
chr12:56280423 | A | AAAAC | 5 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0240 others(2): Show |
5 | HG00280.hp1 HG02572.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+1996_588+1997i others(6): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280423 | |||||||
chr12:56280424 | A | AAAC | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
79 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.588+1995_588+1996i others(5): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280424 | |||||||
chr12:56280425 | C | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
311 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.588+1995G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280425 | |||||||
chr12:56280438 | C | A | 14 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(11): Show |
17 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.588+1982G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280438 | |||||||
chr12:56280440 | A | AAAAACCC | 7 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0254 others(4): Show |
7 | HG01106.hp2 HG01517.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+1979_588+1980i others(9): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280440 | |||||||
chr12:56280440 | A | AAAACCC | 7 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0253 others(4): Show |
9 | HG02040.hp2 HG02083.hp1 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.588+1979_588+1980i others(8): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280440 | |||||||
chr12:56280440 | A | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.588+1980T>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280440 | |||||||
chr12:56280982 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.588+1438C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56280982 | |||||||
chr12:56281206 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.588+1214T>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56281206 | |||||||
chr12:56281267 | T | G | 1 | a0001c0001t0001g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.588+1153A>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56281267 | |||||||
chr12:56281445 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0008g0191 |
2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.588+975G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56281445 | |||||||
chr12:56281527 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.588+893A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56281527 | |||||||
chr12:56281565 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.588+855G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56281565 | |||||||
chr12:56281830 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.588+590C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56281830 | |||||||
chr12:56281922 | G | A | 1 | a0001c0002t0002g0259 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.588+498C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56281922 | |||||||
chr12:56281981 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.588+439G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56281981 | |||||||
chr12:56282015 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0151 |
2 | NA18612.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.588+405G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 6/10 | chr12 | 56282015 | |||||||
chr12:56282697 | C | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.400-89G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 5/10 | chr12 | 56282697 | |||||||
chr12:56283033 | CT | C | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.268-43delA | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 4/10 | chr12 | 56283033 | |||||||
chr12:56283266 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(88): Show |
117 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.268-275G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 4/10 | chr12 | 56283266 | |||||||
chr12:56283477 | G | A | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.267+315C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 4/10 | chr12 | 56283477 | |||||||
chr12:56283614 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.267+178T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 4/10 | chr12 | 56283614 | |||||||
chr12:56284087 | G | A | 1 | a0001c0002t0002g0020 | 2 | HG02040.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.202-230C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284087 | |||||||
chr12:56284108 | G | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0177 |
2 | NA18960.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.202-251C>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284108 | |||||||
chr12:56284176 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0197 others(2): Show |
7 | NA18939.hp2 NA18950.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-319G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284176 | |||||||
chr12:56284195 | T | A | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.202-338A>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284195 | |||||||
chr12:56284273 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.202-416G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284273 | |||||||
chr12:56284319 | C | CAA | 6 | a0001c0002t0002g0021 a0001c0002t0002g0022 a0001c0002t0002g0253 others(3): Show |
8 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-464_202-463dup others(2): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284319 | |||||||
chr12:56284319 | C | CAAA | 6 | a0001c0002t0002g0251 a0001c0002t0002g0252 a0001c0002t0002g0255 others(3): Show |
6 | HG02148.hp1 NA18944.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-465_202-463dup others(3): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284319 | |||||||
chr12:56284319 | CA | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.202-463delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284319 | |||||||
chr12:56284337 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02129.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.202-480T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284337 | |||||||
chr12:56284338 | G | A | 17 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0002t0002g0020 others(14): Show |
20 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.202-481C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284338 | |||||||
chr12:56284551 | T | C | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.202-694A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284551 | |||||||
chr12:56284557 | C | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0240 |
3 | HG00280.hp1 HG01168.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.202-700G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284557 | |||||||
chr12:56284589 | C | CTT | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.202-734_202-733dup others(2): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284589 | |||||||
chr12:56284589 | CT | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0066 a0001c0001t0001g0136 others(4): Show |
7 | HG01256.hp2 HG01358.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-733delA | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284589 | |||||||
chr12:56284630 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.202-773T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284630 | |||||||
chr12:56284665 | G | C | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-808C>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284665 | |||||||
chr12:56284684 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-827C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284684 | |||||||
chr12:56284686 | C | G | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-829G>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284686 | |||||||
chr12:56284689 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-832G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284689 | |||||||
chr12:56284694 | T | G | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-837A>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284694 | |||||||
chr12:56284695 | A | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-838T>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284695 | |||||||
chr12:56284700 | G | GT | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-844_202-843ins others(1): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284700 | |||||||
chr12:56284701 | A | C | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-844T>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284701 | |||||||
chr12:56284704 | T | G | 7 | a0001c0001t0001g0136 a0001c0001t0001g0140 a0001c0001t0001g0167 others(4): Show |
7 | HG00323.hp1 HG01109.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-847A>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284704 | |||||||
chr12:56284709 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-852C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284709 | |||||||
chr12:56284857 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.202-1000A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284857 | |||||||
chr12:56284897 | CA | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.201+1018delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284897 | |||||||
chr12:56284897 | CAA | C | 15 | a0001c0001t0001g0236 a0001c0002t0002g0020 a0001c0002t0002g0021 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.201+1017_201+1018d others(4): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284897 | |||||||
chr12:56284908 | A | C | 1 | a0001c0001t0001g0245 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.201+1008T>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284908 | |||||||
chr12:56284991 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.201+925G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56284991 | |||||||
chr12:56285118 | T | C | 2 | a0001c0001t0005g0090 a0001c0001t0005g0092 |
2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.201+798A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56285118 | |||||||
chr12:56285287 | TTTTG | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0068 a0001c0001t0001g0211 |
4 | NA18946.hp1 NA19005.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+625_201+628del others(4): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56285287 | |||||||
chr12:56285425 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.201+491C>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56285425 | |||||||
chr12:56285543 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.201+373G>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56285543 | |||||||
chr12:56285563 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.201+353A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 3/10 | chr12 | 56285563 | |||||||
chr12:56286187 | A | G | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.94-164T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 2/10 | chr12 | 56286187 | |||||||
chr12:56286747 | T | C | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-102A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56286747 | |||||||
chr12:56286852 | A | G | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-207T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56286852 | |||||||
chr12:56286961 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0149 others(14): Show |
25 | HG00423.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.43-316G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56286961 | |||||||
chr12:56287209 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.43-564C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287209 | |||||||
chr12:56287340 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.43-695C>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287340 | |||||||
chr12:56287479 | C | CA | 12 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0080 others(9): Show |
12 | HG01358.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.43-835dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287479 | CA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
173 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.43-835delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287479 | CAA | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0101 others(11): Show |
14 | HG01169.hp1 HG01515.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-836_43-835delTT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287479 | CAAA | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0103 others(14): Show |
18 | HG00423.hp2 HG01243.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.43-837_43-835delTT others(1): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287479 | CAAAA | C | 8 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0115 others(5): Show |
8 | HG01167.hp1 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-838_43-835delTT others(2): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287479 | CAAAAA | C | 11 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(8): Show |
14 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-839_43-835delTT others(3): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287479 | CAAAAAAA others(3): Show |
C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0070 a0001c0001t0001g0124 others(11): Show |
15 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.43-844_43-835delTT others(8): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287479 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0224 |
2 | HG00738.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.43-845_43-835delTT others(9): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287479 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0183 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.43-847_43-835delTT others(11): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287479 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0075 |
2 | HG02056.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.43-848_43-835delTT others(12): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287479 | |||||||
chr12:56287707 | TGCAATGG others(17): Show |
T | 1 | a0001c0001t0001g0182 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.43-1086_43-1063del others(24): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287707 | |||||||
chr12:56287782 | GTAGCTGG others(3): Show |
G | 1 | a0001c0001t0001g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43-1147_43-1138del others(10): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287782 | |||||||
chr12:56287846 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43-1201G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287846 | |||||||
chr12:56287909 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0046 |
3 | HG00673.hp1 HG02027.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.43-1264G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56287909 | |||||||
chr12:56288018 | C | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0135 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.43-1373G>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288018 | |||||||
chr12:56288090 | C | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0181 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.43-1445G>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288090 | |||||||
chr12:56288196 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.43-1551G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288196 | |||||||
chr12:56288314 | T | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.43-1669A>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288314 | |||||||
chr12:56288346 | A | AT | 27 | a0001c0001t0001g0066 a0001c0001t0001g0074 a0001c0001t0001g0101 others(24): Show |
30 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.43-1702dupA | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288346 | |||||||
chr12:56288346 | AT | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0037 others(22): Show |
29 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.43-1702delA | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288346 | |||||||
chr12:56288360 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02129.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.43-1715A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288360 | |||||||
chr12:56288413 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.43-1768C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288413 | |||||||
chr12:56288587 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.43-1942G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288587 | |||||||
chr12:56288702 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0135 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.43-2057T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288702 | |||||||
chr12:56288817 | TA | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
242 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.43-2173delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288817 | |||||||
chr12:56288830 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.43-2185T>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288830 | |||||||
chr12:56288831 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.43-2186A>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56288831 | |||||||
chr12:56289032 | T | C | 5 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG01109.hp1 HG01256.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-2387A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289032 | |||||||
chr12:56289129 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43-2484A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289129 | |||||||
chr12:56289333 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.43-2688G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289333 | |||||||
chr12:56289423 | A | AT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
75 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.43-2779dupA | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289423 | |||||||
chr12:56289449 | AT | A | 16 | a0001c0001t0001g0019 a0001c0001t0001g0119 a0001c0001t0001g0124 others(13): Show |
17 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.43-2805delA | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289449 | |||||||
chr12:56289688 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.43-3043G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289688 | |||||||
chr12:56289777 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0135 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.43-3132G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289777 | |||||||
chr12:56289864 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.43-3219T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289864 | |||||||
chr12:56289893 | T | C | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG02145.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-3248A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289893 | |||||||
chr12:56289897 | T | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0233 |
2 | HG01243.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.43-3252A>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289897 | |||||||
chr12:56289979 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.43-3334G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289979 | |||||||
chr12:56289997 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.43-3352C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56289997 | |||||||
chr12:56290173 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0017 others(28): Show |
45 | HG00609.hp1 HG00673.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.43-3528C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290173 | |||||||
chr12:56290191 | C | T | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-3546G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290191 | |||||||
chr12:56290373 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.43-3728C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290373 | |||||||
chr12:56290462 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.43-3817C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290462 | |||||||
chr12:56290558 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.43-3913A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290558 | |||||||
chr12:56290628 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.43-3983A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290628 | |||||||
chr12:56290712 | TAGGAA | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.43-4072_43-4068del others(5): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290712 | |||||||
chr12:56290873 | CA | C | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-4229delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290873 | |||||||
chr12:56290903 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0121 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.43-4258C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290903 | |||||||
chr12:56290956 | CCAAA | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0007g0166 |
3 | HG01109.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.43-4315_43-4312del others(4): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56290956 | |||||||
chr12:56291014 | C | T | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-4369G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56291014 | |||||||
chr12:56291128 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
6 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-4483A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56291128 | |||||||
chr12:56291262 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.43-4617T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56291262 | |||||||
chr12:56291326 | G | C | 1 | a0001c0001t0001g0249 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.43-4681C>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56291326 | |||||||
chr12:56291668 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.43-5023G>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56291668 | |||||||
chr12:56292088 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-5443A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56292088 | |||||||
chr12:56292133 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.43-5488G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56292133 | |||||||
chr12:56292389 | T | TA | 8 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0163 others(5): Show |
8 | HG01978.hp1 HG02145.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-5745dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56292389 | |||||||
chr12:56292659 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.43-6014G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56292659 | |||||||
chr12:56292730 | C | CA | 38 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0050 others(35): Show |
41 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.43-6086dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56292730 | |||||||
chr12:56292730 | CA | C | 10 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0066 others(7): Show |
10 | HG01168.hp2 HG01169.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.43-6086delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56292730 | |||||||
chr12:56292730 | CAA | C | 5 | a0001c0002t0002g0020 a0001c0002t0002g0252 a0001c0002t0002g0256 others(2): Show |
6 | HG02040.hp2 HG02083.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-6087_43-6086del others(2): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56292730 | |||||||
chr12:56292730 | CAAA | C | 10 | a0001c0002t0002g0021 a0001c0002t0002g0022 a0001c0002t0002g0251 others(7): Show |
12 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-6088_43-6086del others(3): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56292730 | |||||||
chr12:56292859 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.43-6214C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56292859 | |||||||
chr12:56293093 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.43-6448C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56293093 | |||||||
chr12:56293213 | C | T | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-6568G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56293213 | |||||||
chr12:56293577 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.42+6583G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56293577 | |||||||
chr12:56293675 | T | C | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+6485A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56293675 | |||||||
chr12:56293788 | G | T | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+6372C>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56293788 | |||||||
chr12:56294021 | C | T | 49 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0101 others(46): Show |
51 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(48): Show |
intron_variant | MODIFIER | c.42+6139G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294021 | |||||||
chr12:56294025 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.42+6135C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294025 | |||||||
chr12:56294040 | C | T | 1 | a0001c0001t0013g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.42+6120G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294040 | |||||||
chr12:56294056 | G | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0125 others(11): Show |
15 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.42+6104C>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294056 | |||||||
chr12:56294285 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.42+5875G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294285 | |||||||
chr12:56294453 | G | A | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+5707C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294453 | |||||||
chr12:56294464 | ACT | A | 7 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0026 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.42+5694_42+5695del others(2): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294464 | |||||||
chr12:56294473 | C | CA | 36 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(33): Show |
37 | HG00639.hp2 HG01109.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.42+5686dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294473 | |||||||
chr12:56294473 | CA | C | 19 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0001g0071 others(16): Show |
22 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.42+5686delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294473 | |||||||
chr12:56294479 | A | G | 11 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0168 others(8): Show |
11 | HG01109.hp1 HG01256.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.42+5681T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294479 | |||||||
chr12:56294480 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.42+5680T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56294480 | |||||||
chr12:56295238 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.42+4922G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295238 | |||||||
chr12:56295680 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.42+4480G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295680 | |||||||
chr12:56295711 | G | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.42+4449C>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295711 | |||||||
chr12:56295713 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00639.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.42+4447C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295713 | |||||||
chr12:56295751 | G | A | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+4409C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295751 | |||||||
chr12:56295751 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42+4409C>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295751 | |||||||
chr12:56295771 | G | A | 1 | a0001c0003t0001g0123 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.42+4389C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295771 | |||||||
chr12:56295936 | A | T | 1 | a0001c0001t0001g0249 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.42+4224T>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295936 | |||||||
chr12:56295941 | G | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.42+4219C>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295941 | |||||||
chr12:56295951 | C | CA | 31 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0100 others(28): Show |
33 | HG00673.hp2 HG01243.hp1 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.42+4208dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295951 | |||||||
chr12:56295951 | C | CAA | 6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0121 others(3): Show |
6 | HG01243.hp2 HG01358.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+4207_42+4208dup others(2): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295951 | |||||||
chr12:56295951 | C | CAAAAAAA others(1): Show |
6 | a0001c0002t0002g0021 a0001c0002t0002g0022 a0001c0002t0002g0252 others(3): Show |
8 | HG00642.hp1 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+4201_42+4208dup others(8): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295951 | |||||||
chr12:56295951 | CA | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.42+4208delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295951 | |||||||
chr12:56295951 | CAA | C | 12 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0070 others(9): Show |
12 | HG00673.hp1 HG01109.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+4207_42+4208del others(2): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295951 | |||||||
chr12:56295951 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0101 |
2 | HG02257.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.42+4197_42+4208del others(12): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295951 | |||||||
chr12:56295951 | CAAAAAAA others(9): Show |
C | 1 | a0001c0003t0001g0123 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.42+4193_42+4208del others(16): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56295951 | |||||||
chr12:56296064 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.42+4096C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56296064 | |||||||
chr12:56296333 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | NA18971.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.42+3827G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56296333 | |||||||
chr12:56296536 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.42+3624G>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56296536 | |||||||
chr12:56296553 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.42+3607G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56296553 | |||||||
chr12:56296824 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.42+3336G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56296824 | |||||||
chr12:56296827 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.42+3333A>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56296827 | |||||||
chr12:56296878 | G | A | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+3282C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56296878 | |||||||
chr12:56297816 | T | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
86 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.42+2344A>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56297816 | |||||||
chr12:56297970 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42+2190G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56297970 | |||||||
chr12:56297980 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.42+2180C>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56297980 | |||||||
chr12:56297989 | AC | A | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+2170delG | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56297989 | |||||||
chr12:56298926 | C | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.42+1234G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56298926 | |||||||
chr12:56298976 | A | G | 2 | a0001c0002t0002g0251 a0001c0002t0002g0252 |
2 | NA18944.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.42+1184T>C | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56298976 | |||||||
chr12:56299041 | C | CA | 25 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0064 others(22): Show |
28 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.42+1118dupT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299041 | |||||||
chr12:56299041 | CA | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG01081.hp1 HG01943.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+1118delT | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299041 | |||||||
chr12:56299100 | TC | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0030 others(33): Show |
40 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.42+1059delG | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299100 | |||||||
chr12:56299214 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.42+946G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299214 | |||||||
chr12:56299736 | C | A | 15 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 others(12): Show |
18 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+424G>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299736 | |||||||
chr12:56299774 | CCCTCCAC others(16): Show |
C | 1 | a0001c0001t0001g0262 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.42+363_42+385delAG others(21): Show |
CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299774 | |||||||
chr12:56299852 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.42+308C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299852 | |||||||
chr12:56299877 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.42+283G>A | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299877 | |||||||
chr12:56299951 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.42+209C>T | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299951 | |||||||
chr12:56299951 | G | C | 1 | a0001c0002t0002g0264 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.42+209C>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56299951 | |||||||
chr12:56300123 | A | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01081.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.42+37T>G | CS | ENSG00000062485.19 | transcript | ENST00000351328.8 | protein_coding | 1/10 | chr12 | 56300123 |