Item | Value |
---|---|
geneid | 1643 |
ensemblid | ENSG00000134574.12 |
hgncid | 2718 |
symbol | DDB2 |
name | damage specific DNA binding protein 2 |
refseq_nuc | NM_000107.3 |
refseq_prot | NP_000098.1 |
ensembl_nuc | ENST00000256996.9 |
ensembl_prot | ENSP00000256996.4 |
mane_status | MANE Select |
chr | chr11 |
start | 47214974 |
end | 47239217 |
strand | + |
ver | v1.2 |
region | chr11:47214974-47239217 |
region5000 | chr11:47209974-47244217 |
regionname0 | DDB2_chr11_47214974_47239217 |
regionname5000 | DDB2_chr11_47209974_47244217 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 427 | 357 | 90 | 76 | 130 | 16 | 43 | 112 | DDB2_chr11_47209974_47244217 | DDB2 | MAPKK others(422): Show |
chr11 | 47209974 | 47244217 |
a0002 | 0/0 | 427 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | MAPKK others(422): Show |
chr11 | 47209974 | 47244217 |
a0003 | 0/0 | 427 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | MAPKK others(422): Show |
chr11 | 47209974 | 47244217 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1281 | 349 | 85 | 74 | 129 | 16 | 43 | DDB2_chr11_47209974_47244217 | DDB2 | ATGGC others(1276): Show |
chr11 | 47209974 | 47244217 | ||
a0001c0002 | 0/0 | 1281 | 4 | 4 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | ATGGC others(1276): Show |
chr11 | 47209974 | 47244217 | ||
a0001c0004 | 0/0 | 1281 | 2 | 0 | 2 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | ATGGC others(1276): Show |
chr11 | 47209974 | 47244217 | ||
a0001c0006 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | ATGGC others(1276): Show |
chr11 | 47209974 | 47244217 | ||
a0001c0007 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | ATGGC others(1276): Show |
chr11 | 47209974 | 47244217 | ||
a0002c0003 | 0/0 | 1281 | 2 | 2 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | ATGGC others(1276): Show |
chr11 | 47209974 | 47244217 | ||
a0003c0005 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | ATGGC others(1276): Show |
chr11 | 47209974 | 47244217 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1815 | 286 | 44 | 69 | 117 | 13 | 41 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
a0001c0001t0002 | 0/0 | 1815 | 42 | 38 | 4 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
a0001c0001t0003 | 0/0 | 1815 | 17 | 0 | 1 | 11 | 3 | 2 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
a0001c0001t0004 | 0/0 | 1813 | 3 | 3 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1808): Show |
chr11 | 47209974 | 47244217 |
a0001c0001t0005 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
a0001c0002t0001 | 0/0 | 1815 | 4 | 4 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
a0001c0004t0001 | 0/0 | 1815 | 2 | 0 | 2 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
a0001c0006t0001 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
a0001c0007t0001 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
a0002c0003t0002 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
a0003c0005t0001 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | GGTTT others(1810): Show |
chr11 | 47209974 | 47244217 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 14 | 0 | 3 | 8 | 0 | 2 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0008 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0004t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0004t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0006t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0001c0007t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0002c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0002c0003t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
a0003c0005t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0193 | EUR | GBR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | FIN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | FIN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | CHS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0160 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01261 | hp2 | a0001 | c0004 | t0001 | g0012 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0029 | EUR | IBS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0031 | EUR | IBS | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | CDX | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02451 | hp2 | a0001 | c0006 | t0001 | g0228 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0064 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0222 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02897 | hp2 | a0002 | c0003 | t0002 | g0221 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0189 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04115 | hp1 | a0003 | c0005 | t0001 | g0185 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | YRI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19010 | hp1 | a0001 | c0007 | t0001 | g0147 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | LWK | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | LWK | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | LWK | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | YRI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ASW | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | GIH | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | MSL | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | USA | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | USA | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | USA | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0075 | REF | REF | DDB2_chr11_47209974_47244217 | DDB2 | chr11 | 47209974 | 47244217 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47216426 | T | A | 1 | a0003 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.218T>A | p.Leu73His | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 2/10 | 381/1815 | 218/1284 | 73/427 | chr11 | 47216426 | |||
chr11:47234614 | T | C | 1 | a0002 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.644T>C | p.Met215Thr | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 5/10 | 807/1815 | 644/1284 | 215/427 | chr11 | 47234614 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47216397 | G | T | 1 | a0001c0007 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.189G>T | p.Leu63Leu | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 2/10 | 352/1815 | 189/1284 | 63/427 | chr11 | 47216397 | |||
chr11:47216971 | C | T | 1 | a0001c0002 | 4 | HG02615.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.378C>T | p.Thr126Thr | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/10 | 541/1815 | 378/1284 | 126/427 | chr11 | 47216971 | |||
chr11:47234792 | G | A | 1 | a0001c0004 | 2 | HG01175.hp1 HG01261.hp2 |
synonymous_variant | LOW | c.738G>A | p.Thr246Thr | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 6/10 | 901/1815 | 738/1284 | 246/427 | chr11 | 47234792 | |||
chr11:47235283 | C | T | 1 | a0001c0006 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.894C>T | p.Pro298Pro | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/10 | 1057/1815 | 894/1284 | 298/427 | chr11 | 47235283 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47215017 | G | A | 2 | a0001c0001t0002 a0002c0003t0002 |
44 | HG01109.hp1 HG01243.hp1 HG01261.hp1 others(41): Show |
5_prime_UTR_variant | MODIFIER | c.-120G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 1/10 | 120 | chr11 | 47215017 | ||||||
chr11:47238872 | C | T | 1 | a0001c0001t0005 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*23C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 10/10 | 23 | chr11 | 47238872 | ||||||
chr11:47238926 | C | T | 1 | a0001c0001t0003 | 17 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 10/10 | 77 | chr11 | 47238926 | ||||||
chr11:47239181 | TCA | T | 1 | a0001c0001t0004 | 3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*334_*335delAC | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 10/10 | 334 | INFO_REALIGN_3_PRIME | chr11 | 47239181 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47215808 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0295 others(5): Show |
10 | HG00735.hp2 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.128-528C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 1/9 | chr11 | 47215808 | |||||||
chr11:47215866 | C | A | 3 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0031 |
3 | HG01516.hp1 HG01517.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.128-470C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 1/9 | chr11 | 47215866 | |||||||
chr11:47216129 | T | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(32): Show |
41 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.128-207T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 1/9 | chr11 | 47216129 | |||||||
chr11:47216252 | T | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.128-84T>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 1/9 | chr11 | 47216252 | |||||||
chr11:47216270 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.128-66C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 1/9 | chr11 | 47216270 | |||||||
chr11:47216531 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.264+59T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 2/9 | chr11 | 47216531 | |||||||
chr11:47216580 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.264+108C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 2/9 | chr11 | 47216580 | |||||||
chr11:47216592 | CTG | C | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+123_264+124del others(2): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 47216592 | ||||||
chr11:47216698 | T | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
5 | NA18947.hp2 NA18986.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-160T>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 2/9 | chr11 | 47216698 | |||||||
chr11:47217114 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.456+65A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47217114 | |||||||
chr11:47217267 | T | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00621.hp2 HG00673.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+218T>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47217267 | |||||||
chr11:47217362 | G | A | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.456+313G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47217362 | |||||||
chr11:47217618 | G | T | 1 | a0001c0001t0001g0293 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.456+569G>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47217618 | |||||||
chr11:47217719 | G | A | 23 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0083 others(20): Show |
26 | HG00438.hp2 HG00642.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.456+670G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47217719 | |||||||
chr11:47217877 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02129.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.456+828C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47217877 | |||||||
chr11:47217889 | T | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | NA18942.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.456+840T>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47217889 | |||||||
chr11:47217890 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02280.hp1 HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.456+841C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47217890 | |||||||
chr11:47217892 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.456+843A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47217892 | |||||||
chr11:47218288 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.456+1239G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47218288 | |||||||
chr11:47218939 | A | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(99): Show |
132 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.456+1890A>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47218939 | |||||||
chr11:47218967 | C | T | 23 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0021 others(20): Show |
28 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.456+1918C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47218967 | |||||||
chr11:47219093 | T | C | 1 | a0001c0001t0002g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.456+2044T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47219093 | |||||||
chr11:47219292 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.456+2243C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47219292 | |||||||
chr11:47219323 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.456+2274C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47219323 | |||||||
chr11:47219471 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0289 |
3 | HG02965.hp1 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.456+2422C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47219471 | |||||||
chr11:47219493 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.456+2444A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47219493 | |||||||
chr11:47220010 | C | T | 2 | a0001c0001t0002g0009 a0001c0001t0002g0223 |
4 | HG02258.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+2961C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47220010 | |||||||
chr11:47220144 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0289 |
3 | HG02965.hp1 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.456+3095G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47220144 | |||||||
chr11:47220192 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.456+3143C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47220192 | |||||||
chr11:47220229 | A | G | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.456+3180A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47220229 | |||||||
chr11:47220560 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18951.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.456+3511A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47220560 | |||||||
chr11:47220561 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.456+3512C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47220561 | |||||||
chr11:47220766 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.456+3717C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47220766 | |||||||
chr11:47220920 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.456+3871G>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47220920 | |||||||
chr11:47220921 | A | G | 134 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.456+3872A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47220921 | |||||||
chr11:47221035 | C | T | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.456+3986C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221035 | |||||||
chr11:47221149 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.456+4100T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221149 | |||||||
chr11:47221188 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.456+4139A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221188 | |||||||
chr11:47221210 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(121): Show |
157 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.456+4161G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221210 | |||||||
chr11:47221276 | A | AT | 10 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0198 others(7): Show |
12 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.456+4240dupT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47221276 | ||||||
chr11:47221401 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.456+4352G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221401 | |||||||
chr11:47221491 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.456+4442C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221491 | |||||||
chr11:47221783 | A | G | 1 | a0001c0001t0004g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.456+4734A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221783 | |||||||
chr11:47221832 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG01109.hp2 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.456+4783C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221832 | |||||||
chr11:47221873 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.456+4824A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221873 | |||||||
chr11:47221876 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.456+4827C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47221876 | |||||||
chr11:47222114 | G | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
118 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.456+5065G>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47222114 | |||||||
chr11:47222140 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.456+5091C>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47222140 | |||||||
chr11:47222186 | ACTG | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0223 |
4 | HG02258.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+5141_456+5143d others(5): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47222186 | ||||||
chr11:47222587 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.456+5538C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47222587 | |||||||
chr11:47223244 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.456+6195G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223244 | |||||||
chr11:47223304 | G | T | 1 | a0001c0001t0003g0161 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.456+6255G>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223304 | |||||||
chr11:47223333 | A | G | 2 | a0002c0003t0002g0221 a0002c0003t0002g0222 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.456+6284A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223333 | |||||||
chr11:47223378 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.456+6329G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223378 | |||||||
chr11:47223430 | C | T | 18 | a0001c0001t0001g0281 a0001c0001t0003g0029 a0001c0001t0003g0030 others(15): Show |
18 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.456+6381C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223430 | |||||||
chr11:47223534 | G | A | 9 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(6): Show |
9 | HG00438.hp1 HG02451.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.456+6485G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223534 | |||||||
chr11:47223562 | C | T | 1 | a0001c0004t0001g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.456+6513C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223562 | |||||||
chr11:47223594 | C | T | 27 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0054 others(24): Show |
30 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.456+6545C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223594 | |||||||
chr11:47223643 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.456+6594G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223643 | |||||||
chr11:47223655 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.456+6606G>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223655 | |||||||
chr11:47223656 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.456+6607C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223656 | |||||||
chr11:47223660 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.456+6611T>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223660 | |||||||
chr11:47223734 | A | G | 2 | a0001c0001t0001g0290 a0001c0001t0001g0292 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.456+6685A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223734 | |||||||
chr11:47223823 | A | C | 1 | a0001c0001t0001g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.456+6774A>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223823 | |||||||
chr11:47223838 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(94): Show |
135 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(132): Show |
intron_variant | MODIFIER | c.456+6789T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223838 | |||||||
chr11:47223908 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.456+6859C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223908 | |||||||
chr11:47223943 | A | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(94): Show |
135 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(132): Show |
intron_variant | MODIFIER | c.456+6894A>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47223943 | |||||||
chr11:47224250 | C | G | 1 | a0001c0001t0004g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.456+7201C>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47224250 | |||||||
chr11:47224252 | A | G | 192 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.456+7203A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47224252 | |||||||
chr11:47224353 | C | A | 1 | a0001c0001t0001g0013 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.456+7304C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47224353 | |||||||
chr11:47224673 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.456+7624C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47224673 | |||||||
chr11:47224761 | TTC | T | 17 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0031 others(14): Show |
17 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.456+7720_456+7721d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47224761 | ||||||
chr11:47224840 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.456+7791C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47224840 | |||||||
chr11:47224846 | G | A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
167 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.456+7797G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47224846 | |||||||
chr11:47224991 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0054 others(24): Show |
30 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.457-7823G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47224991 | |||||||
chr11:47225189 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.457-7625C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225189 | |||||||
chr11:47225248 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.457-7566T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225248 | |||||||
chr11:47225254 | TA | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
197 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.457-7543delA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47225254 | ||||||
chr11:47225298 | A | T | 1 | a0001c0001t0003g0276 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.457-7516A>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225298 | |||||||
chr11:47225306 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.457-7508T>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225306 | |||||||
chr11:47225389 | G | A | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-7425G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225389 | |||||||
chr11:47225419 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.457-7395C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225419 | |||||||
chr11:47225434 | C | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
197 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.457-7380C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225434 | |||||||
chr11:47225451 | G | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0054 others(23): Show |
29 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.457-7363G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225451 | |||||||
chr11:47225597 | T | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0088 a0001c0001t0001g0128 others(3): Show |
6 | HG01952.hp1 HG02148.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.457-7217T>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225597 | |||||||
chr11:47225687 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.457-7127A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225687 | |||||||
chr11:47225736 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(97): Show |
138 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.457-7078C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225736 | |||||||
chr11:47225737 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.457-7077T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47225737 | |||||||
chr11:47226009 | A | C | 194 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.457-6805A>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226009 | |||||||
chr11:47226070 | G | A | 165 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
187 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.457-6744G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226070 | |||||||
chr11:47226134 | C | T | 2 | a0002c0003t0002g0221 a0002c0003t0002g0222 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.457-6680C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226134 | |||||||
chr11:47226136 | A | C | 1 | a0001c0001t0001g0291 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.457-6678A>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226136 | |||||||
chr11:47226158 | T | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.457-6656T>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226158 | |||||||
chr11:47226273 | A | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0289 |
3 | HG02965.hp1 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.457-6541A>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226273 | |||||||
chr11:47226278 | C | CTTT | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(83): Show |
96 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.457-6523_457-6521d others(5): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226278 | ||||||
chr11:47226278 | CT | C | 10 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0089 others(7): Show |
10 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.457-6521delT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226278 | ||||||
chr11:47226285 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457-6529T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226285 | |||||||
chr11:47226332 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.457-6482G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226332 | |||||||
chr11:47226376 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.457-6438A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226376 | |||||||
chr11:47226407 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.457-6407G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226407 | |||||||
chr11:47226499 | C | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
197 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.457-6315C>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226499 | |||||||
chr11:47226639 | A | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0066 others(8): Show |
14 | NA18939.hp2 NA18941.hp2 NA18951.hp1 others(11): Show |
intron_variant | MODIFIER | c.457-6175A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226639 | |||||||
chr11:47226713 | A | G | 7 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.457-6101A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226713 | |||||||
chr11:47226734 | C | CT | 10 | a0001c0001t0001g0088 a0001c0001t0001g0103 a0001c0001t0001g0116 others(7): Show |
10 | HG02257.hp2 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.457-6055dupT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226734 | ||||||
chr11:47226734 | CT | C | 11 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0233 others(8): Show |
11 | HG01070.hp1 HG01081.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.457-6055delT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226734 | ||||||
chr11:47226734 | CTT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(79): Show |
120 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.457-6056_457-6055d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226734 | ||||||
chr11:47226734 | CTTT | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0067 a0001c0001t0001g0232 others(3): Show |
6 | HG02723.hp1 HG03041.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-6057_457-6055d others(5): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226734 | ||||||
chr11:47226734 | CTTTTTTT others(5): Show |
C | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(122): Show |
135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.457-6066_457-6055d others(14): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226734 | ||||||
chr11:47226734 | CTTTTTTT others(6): Show |
C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(26): Show |
38 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.457-6067_457-6055d others(15): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226734 | ||||||
chr11:47226734 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0165 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.457-6068_457-6055d others(16): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226734 | ||||||
chr11:47226909 | CTTTGT | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG01109.hp2 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.457-5891_457-5887d others(7): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47226909 | ||||||
chr11:47226971 | A | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0289 |
3 | HG02965.hp1 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.457-5843A>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47226971 | |||||||
chr11:47227099 | C | CT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(104): Show |
144 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.457-5691dupT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47227099 | ||||||
chr11:47227099 | C | CTT | 122 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
142 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.457-5692_457-5691d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47227099 | ||||||
chr11:47227099 | C | CTTT | 58 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0049 others(55): Show |
60 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.457-5693_457-5691d others(5): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47227099 | ||||||
chr11:47227099 | C | CTTTT | 5 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0100 others(2): Show |
6 | HG00438.hp2 HG01192.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-5694_457-5691d others(6): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47227099 | ||||||
chr11:47227099 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0126 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.457-5701_457-5691d others(13): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47227099 | ||||||
chr11:47227132 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.457-5682G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47227132 | |||||||
chr11:47227398 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.457-5416C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47227398 | |||||||
chr11:47227505 | AT | A | 9 | a0001c0001t0001g0038 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
9 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.457-5293delT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47227505 | ||||||
chr11:47227672 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(25): Show |
36 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.457-5142G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47227672 | |||||||
chr11:47227727 | C | T | 2 | a0001c0001t0002g0111 a0001c0001t0002g0112 |
2 | HG01261.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.457-5087C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47227727 | |||||||
chr11:47227743 | G | A | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
197 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.457-5071G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47227743 | |||||||
chr11:47227869 | T | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.457-4945T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47227869 | |||||||
chr11:47227912 | G | C | 192 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.457-4902G>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47227912 | |||||||
chr11:47227985 | C | T | 2 | a0001c0001t0001g0186 a0003c0005t0001g0185 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.457-4829C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47227985 | |||||||
chr11:47228023 | C | T | 2 | a0002c0003t0002g0221 a0002c0003t0002g0222 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.457-4791C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228023 | |||||||
chr11:47228138 | C | CA | 23 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0039 others(20): Show |
25 | HG00621.hp2 HG01361.hp1 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.457-4654dupA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228138 | ||||||
chr11:47228138 | CA | C | 58 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0033 others(55): Show |
61 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.457-4654delA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228138 | ||||||
chr11:47228266 | C | CA | 7 | a0001c0001t0001g0187 a0001c0001t0001g0240 a0001c0001t0001g0241 others(4): Show |
7 | HG02738.hp2 HG02818.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.457-4534dupA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228266 | ||||||
chr11:47228266 | CA | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0060 others(6): Show |
10 | HG00099.hp1 HG01070.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.457-4534delA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228266 | ||||||
chr11:47228337 | G | A | 1 | a0001c0006t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.457-4477G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228337 | |||||||
chr11:47228367 | G | GT | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.457-4447_457-4446i others(3): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228367 | |||||||
chr11:47228368 | C | CG | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(93): Show |
134 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.457-4444dupG | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228368 | ||||||
chr11:47228368 | C | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.457-4446C>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228368 | |||||||
chr11:47228536 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0116 |
2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.457-4278G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228536 | |||||||
chr11:47228573 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.457-4241G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228573 | |||||||
chr11:47228642 | C | CA | 16 | a0001c0001t0001g0054 a0001c0001t0001g0084 a0001c0001t0001g0166 others(13): Show |
16 | HG00609.hp2 HG01192.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.457-4154dupA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228642 | ||||||
chr11:47228642 | C | CAA | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-4155_457-4154d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228642 | ||||||
chr11:47228642 | C | CAAAAA | 17 | a0001c0001t0001g0281 a0001c0001t0003g0029 a0001c0001t0003g0030 others(14): Show |
17 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.457-4158_457-4154d others(7): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228642 | ||||||
chr11:47228722 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.457-4092C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228722 | |||||||
chr11:47228732 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0072 |
3 | NA18986.hp1 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.457-4082G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228732 | |||||||
chr11:47228768 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(26): Show |
37 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.457-4046C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228768 | |||||||
chr11:47228825 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.457-3989C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228825 | |||||||
chr11:47228956 | C | CA | 57 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(54): Show |
80 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.457-3841dupA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228956 | ||||||
chr11:47228956 | C | CAA | 34 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0036 others(31): Show |
37 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.457-3842_457-3841d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228956 | ||||||
chr11:47228956 | C | CAAA | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.457-3843_457-3841d others(5): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228956 | ||||||
chr11:47228974 | G | A | 8 | a0001c0001t0001g0240 a0001c0001t0001g0272 a0001c0001t0002g0214 others(5): Show |
8 | HG01109.hp1 HG01884.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.457-3840G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228974 | |||||||
chr11:47228976 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.457-3838A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228976 | |||||||
chr11:47228977 | A | AGAAATAT others(1): Show |
4 | a0001c0001t0002g0214 a0001c0001t0002g0217 a0001c0001t0002g0218 others(1): Show |
4 | HG01109.hp1 HG03540.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.457-3837_457-3836i others(10): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228977 | |||||||
chr11:47228977 | A | AGAAATAT others(5): Show |
1 | a0001c0001t0002g0216 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.457-3837_457-3836i others(14): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228977 | |||||||
chr11:47228977 | A | AGAAATAT others(13): Show |
2 | a0001c0001t0001g0272 a0001c0001t0002g0215 |
2 | HG02071.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.457-3837_457-3836i others(22): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228977 | |||||||
chr11:47228977 | A | ATATC | 13 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0052 others(10): Show |
13 | HG00323.hp1 HG00642.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.457-3795_457-3792d others(6): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228977 | ||||||
chr11:47228977 | A | ATATCTAT others(1): Show |
47 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0032 others(44): Show |
49 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.457-3799_457-3792d others(10): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228977 | ||||||
chr11:47228977 | A | ATATCTAT others(5): Show |
51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(48): Show |
55 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.457-3803_457-3792d others(14): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228977 | ||||||
chr11:47228977 | A | ATATCTAT others(9): Show |
72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
87 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.457-3807_457-3792d others(18): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228977 | ||||||
chr11:47228977 | A | ATATCTAT others(13): Show |
5 | a0001c0001t0001g0040 a0001c0001t0001g0154 a0001c0001t0001g0167 others(2): Show |
5 | HG01099.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.457-3811_457-3792d others(22): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228977 | ||||||
chr11:47228977 | ATATC | A | 40 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0023 others(37): Show |
51 | HG00280.hp2 HG01243.hp2 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.457-3795_457-3792d others(6): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228977 | ||||||
chr11:47228977 | ATATCTAT others(1): Show |
A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(42): Show |
71 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.457-3799_457-3792d others(10): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228977 | ||||||
chr11:47228977 | ATATCTAT others(9): Show |
A | 1 | a0001c0001t0001g0034 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.457-3807_457-3792d others(18): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47228977 | ||||||
chr11:47228978 | T | A | 1 | a0001c0001t0001g0240 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.457-3836T>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228978 | |||||||
chr11:47228978 | T | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0258 |
2 | HG02602.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.457-3836T>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228978 | |||||||
chr11:47228980 | T | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0258 |
2 | HG02602.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.457-3834T>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228980 | |||||||
chr11:47228981 | C | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0258 |
2 | HG02602.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.457-3833C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47228981 | |||||||
chr11:47229106 | C | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0002g0213 |
3 | HG02257.hp2 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.457-3708C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47229106 | |||||||
chr11:47229256 | A | C | 18 | a0001c0001t0001g0281 a0001c0001t0003g0029 a0001c0001t0003g0030 others(15): Show |
18 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.457-3558A>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47229256 | |||||||
chr11:47229257 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.457-3557G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47229257 | |||||||
chr11:47229294 | C | T | 18 | a0001c0001t0001g0281 a0001c0001t0003g0029 a0001c0001t0003g0030 others(15): Show |
18 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.457-3520C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47229294 | |||||||
chr11:47229316 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG01109.hp2 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.457-3498C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47229316 | |||||||
chr11:47229595 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.457-3219C>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47229595 | |||||||
chr11:47229630 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.457-3184A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47229630 | |||||||
chr11:47229648 | G | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
171 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.457-3166G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47229648 | |||||||
chr11:47229818 | C | CT | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.457-2979dupT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47229818 | ||||||
chr11:47230055 | TGGGACGT others(10): Show |
T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0054 others(23): Show |
29 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.457-2756_457-2740d others(19): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47230055 | ||||||
chr11:47230101 | T | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.457-2713T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230101 | |||||||
chr11:47230132 | T | TA | 18 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0048 others(15): Show |
19 | HG00741.hp2 HG02145.hp1 HG02148.hp1 others(16): Show |
intron_variant | MODIFIER | c.457-2661dupA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47230132 | ||||||
chr11:47230132 | T | TAA | 18 | a0001c0001t0001g0281 a0001c0001t0003g0029 a0001c0001t0003g0030 others(15): Show |
18 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.457-2662_457-2661d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47230132 | ||||||
chr11:47230132 | TA | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0267 a0001c0001t0001g0298 others(4): Show |
7 | HG00639.hp1 HG01099.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.457-2661delA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47230132 | ||||||
chr11:47230198 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.457-2616G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230198 | |||||||
chr11:47230240 | C | T | 5 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0031 others(2): Show |
5 | HG00099.hp1 HG01433.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.457-2574C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230240 | |||||||
chr11:47230556 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0038 others(4): Show |
8 | HG00323.hp1 HG01255.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.457-2258G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230556 | |||||||
chr11:47230599 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.457-2215A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230599 | |||||||
chr11:47230686 | T | A | 18 | a0001c0001t0001g0281 a0001c0001t0003g0029 a0001c0001t0003g0030 others(15): Show |
18 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.457-2128T>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230686 | |||||||
chr11:47230694 | C | T | 1 | a0001c0002t0001g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.457-2120C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230694 | |||||||
chr11:47230703 | T | C | 18 | a0001c0001t0001g0281 a0001c0001t0003g0029 a0001c0001t0003g0030 others(15): Show |
18 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.457-2111T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230703 | |||||||
chr11:47230753 | G | A | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.457-2061G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230753 | |||||||
chr11:47230835 | G | A | 2 | a0001c0002t0001g0074 a0001c0002t0001g0076 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.457-1979G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230835 | |||||||
chr11:47230905 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.457-1909G>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230905 | |||||||
chr11:47230996 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0258 |
2 | NA18956.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.457-1818T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47230996 | |||||||
chr11:47231013 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.457-1801A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47231013 | |||||||
chr11:47231119 | C | CA | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(85): Show |
99 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.457-1670dupA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47231119 | ||||||
chr11:47231119 | C | CAA | 24 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0048 others(21): Show |
24 | HG00673.hp1 HG01109.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.457-1671_457-1670d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47231119 | ||||||
chr11:47231119 | CA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(72): Show |
112 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.457-1670delA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47231119 | ||||||
chr11:47231119 | CAA | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0055 others(23): Show |
29 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.457-1671_457-1670d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47231119 | ||||||
chr11:47231143 | A | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0054 others(24): Show |
30 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.457-1671A>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47231143 | |||||||
chr11:47231144 | A | C | 2 | a0001c0001t0003g0274 a0001c0001t0003g0275 |
2 | NA18956.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.457-1670A>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47231144 | |||||||
chr11:47231248 | A | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.457-1566A>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47231248 | |||||||
chr11:47231249 | T | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.457-1565T>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47231249 | |||||||
chr11:47231524 | T | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0047 others(28): Show |
34 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.457-1290T>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47231524 | |||||||
chr11:47231586 | C | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0054 others(23): Show |
29 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.457-1228C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47231586 | |||||||
chr11:47231693 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(90): Show |
131 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(128): Show |
intron_variant | MODIFIER | c.457-1121T>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47231693 | |||||||
chr11:47231759 | A | G | 18 | a0001c0001t0001g0281 a0001c0001t0003g0029 a0001c0001t0003g0030 others(15): Show |
18 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.457-1055A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47231759 | |||||||
chr11:47232089 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.457-725A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47232089 | |||||||
chr11:47232194 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.457-620T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47232194 | |||||||
chr11:47232383 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 |
3 | HG02723.hp1 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.457-431G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47232383 | |||||||
chr11:47232428 | G | T | 2 | a0001c0001t0002g0009 a0001c0001t0002g0223 |
4 | HG02258.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.457-386G>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47232428 | |||||||
chr11:47232459 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(94): Show |
135 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(132): Show |
intron_variant | MODIFIER | c.457-355T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47232459 | |||||||
chr11:47232485 | T | TA | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(108): Show |
149 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.457-317dupA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 47232485 | ||||||
chr11:47232500 | G | C | 196 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.457-314G>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47232500 | |||||||
chr11:47232737 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.457-77G>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47232737 | |||||||
chr11:47232783 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.457-31C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 3/9 | chr11 | 47232783 | |||||||
chr11:47232979 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG01109.hp2 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.602+20G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47232979 | |||||||
chr11:47233051 | G | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0105 a0001c0001t0002g0106 others(4): Show |
12 | HG02109.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.602+92G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233051 | |||||||
chr11:47233148 | C | T | 9 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(6): Show |
9 | HG02486.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.602+189C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233148 | |||||||
chr11:47233394 | G | A | 1 | a0001c0001t0003g0194 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.602+435G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233394 | |||||||
chr11:47233470 | C | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.602+511C>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233470 | |||||||
chr11:47233568 | C | T | 7 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.602+609C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233568 | |||||||
chr11:47233619 | G | A | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0004g0065 |
3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.602+660G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233619 | |||||||
chr11:47233709 | CA | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
170 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.602+768delA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 47233709 | ||||||
chr11:47233709 | CAA | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(94): Show |
136 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.602+767_602+768del others(2): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 47233709 | ||||||
chr11:47233766 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(90): Show |
131 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(128): Show |
intron_variant | MODIFIER | c.602+807G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233766 | |||||||
chr11:47233795 | G | C | 1 | a0001c0001t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.603-778G>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233795 | |||||||
chr11:47233845 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.603-728G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233845 | |||||||
chr11:47233865 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.603-708C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233865 | |||||||
chr11:47233866 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0292 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.603-707G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233866 | |||||||
chr11:47233945 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.603-628C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47233945 | |||||||
chr11:47234018 | G | C | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(8): Show |
11 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.603-555G>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47234018 | |||||||
chr11:47234038 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.603-535G>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47234038 | |||||||
chr11:47234047 | T | C | 188 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.603-526T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47234047 | |||||||
chr11:47234262 | TG | T | 19 | a0001c0001t0001g0062 a0001c0001t0001g0236 a0001c0001t0003g0029 others(16): Show |
19 | HG00099.hp1 HG00621.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.603-305delG | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 47234262 | ||||||
chr11:47234352 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.603-221A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47234352 | |||||||
chr11:47234423 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.603-150C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47234423 | |||||||
chr11:47234427 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.603-146C>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47234427 | |||||||
chr11:47234438 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0289 |
3 | HG02965.hp1 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.603-135C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47234438 | |||||||
chr11:47234552 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.603-21C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 4/9 | chr11 | 47234552 | |||||||
chr11:47234973 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.880+39C>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 6/9 | chr11 | 47234973 | |||||||
chr11:47235131 | A | G | 17 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0031 others(14): Show |
17 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.881-139A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 6/9 | chr11 | 47235131 | |||||||
chr11:47235157 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(93): Show |
134 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.881-113C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 6/9 | chr11 | 47235157 | |||||||
chr11:47235765 | TA | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0289 |
3 | HG02965.hp1 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1023+354delA | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47235765 | |||||||
chr11:47235789 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(87): Show |
128 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.1023+377C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47235789 | |||||||
chr11:47235875 | C | CT | 10 | a0001c0001t0001g0270 a0001c0001t0001g0282 a0001c0001t0001g0283 others(7): Show |
10 | HG02486.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1023+476dupT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 47235875 | ||||||
chr11:47235926 | C | CT | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
255 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.1023+537dupT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 47235926 | ||||||
chr11:47235926 | C | CTT | 62 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(59): Show |
71 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1023+536_1023+537d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 47235926 | ||||||
chr11:47235926 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1023+526_1023+537d others(14): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 47235926 | ||||||
chr11:47235959 | G | GTC | 18 | a0001c0001t0001g0281 a0001c0001t0003g0029 a0001c0001t0003g0030 others(15): Show |
18 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1023+549_1023+550d others(4): Show |
DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 47235959 | ||||||
chr11:47236082 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1023+670G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47236082 | |||||||
chr11:47236679 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0292 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1024-1158G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47236679 | |||||||
chr11:47236817 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0153 |
2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1024-1020C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47236817 | |||||||
chr11:47236818 | G | A | 17 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0031 others(14): Show |
17 | HG00099.hp1 HG00621.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1024-1019G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47236818 | |||||||
chr11:47236995 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1024-842T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47236995 | |||||||
chr11:47237056 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1024-781G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47237056 | |||||||
chr11:47237265 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1024-572T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47237265 | |||||||
chr11:47237302 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(90): Show |
131 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(128): Show |
intron_variant | MODIFIER | c.1024-535C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47237302 | |||||||
chr11:47237308 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1024-529G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47237308 | |||||||
chr11:47237428 | A | C | 11 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0126 others(8): Show |
12 | HG03831.hp2 HG04204.hp1 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1024-409A>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47237428 | |||||||
chr11:47237434 | C | CT | 14 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(11): Show |
14 | HG01071.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1024-385dupT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 47237434 | ||||||
chr11:47237713 | G | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(93): Show |
134 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.1024-124G>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 7/9 | chr11 | 47237713 | |||||||
chr11:47238117 | T | C | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1189-21T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 8/9 | chr11 | 47238117 | |||||||
chr11:47238260 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1234+77C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238260 | |||||||
chr11:47238263 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1234+80G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238263 | |||||||
chr11:47238300 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1234+117G>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238300 | |||||||
chr11:47238403 | C | CT | 17 | a0001c0001t0001g0101 a0001c0001t0001g0253 a0001c0001t0001g0281 others(14): Show |
17 | HG00099.hp1 HG00609.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1234+232dupT | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 47238403 | ||||||
chr11:47238428 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1234+245C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238428 | |||||||
chr11:47238442 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(111): Show |
152 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(149): Show |
intron_variant | MODIFIER | c.1234+259G>A | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238442 | |||||||
chr11:47238474 | A | G | 2 | a0002c0003t0002g0221 a0002c0003t0002g0222 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1234+291A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238474 | |||||||
chr11:47238591 | G | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0054 others(25): Show |
31 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1235-209G>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238591 | |||||||
chr11:47238687 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1235-113C>T | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238687 | |||||||
chr11:47238721 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(147): Show |
191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1235-79T>C | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238721 | |||||||
chr11:47238768 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(149): Show |
193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1235-32A>G | DDB2 | ENSG00000134574.12 | transcript | ENST00000256996.9 | protein_coding | 9/9 | chr11 | 47238768 |