Item | Value |
---|---|
geneid | 51389 |
ensemblid | ENSG00000111832.13 |
hgncid | 20993 |
symbol | RWDD1 |
name | RWD domain containing 1 |
refseq_nuc | NM_015952.4 |
refseq_prot | NP_057036.2 |
ensembl_nuc | ENST00000466444.7 |
ensembl_prot | ENSP00000420357.2 |
mane_status | MANE Select |
chr | chr6 |
start | 116571504 |
end | 116597675 |
strand | + |
ver | v1.2 |
region | chr6:116571504-116597675 |
region5000 | chr6:116566504-116602675 |
regionname0 | RWDD1_chr6_116571504_116597675 |
regionname5000 | RWDD1_chr6_116566504_116602675 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 243 | 377 | 88 | 56 | 171 | 18 | 42 | 136 | RWDD1_chr6_116566504_116602675 | RWDD1 | MTDYG others(238): Show |
chr6 | 116566504 | 116602675 |
a0002 | 0/0 | 243 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | MTDYG others(238): Show |
chr6 | 116566504 | 116602675 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 729 | 377 | 88 | 56 | 171 | 18 | 42 | RWDD1_chr6_116566504_116602675 | RWDD1 | ATGAC others(724): Show |
chr6 | 116566504 | 116602675 | ||
a0002c0002 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | ATGAC others(724): Show |
chr6 | 116566504 | 116602675 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5385 | 83 | 3 | 16 | 51 | 6 | 7 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0002 | 0/0 | 5385 | 82 | 6 | 13 | 52 | 5 | 6 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0003 | 1/0 | 5385 | 48 | 10 | 4 | 29 | 2 | 2 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0004 | 0/1 | 5385 | 40 | 15 | 11 | 4 | 1 | 8 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0005 | 0/0 | 5385 | 19 | 6 | 1 | 11 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0006 | 0/0 | 5385 | 10 | 9 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0007 | 0/0 | 5385 | 10 | 6 | 0 | 1 | 0 | 3 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0008 | 0/0 | 5386 | 8 | 8 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5381): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0009 | 0/0 | 5385 | 7 | 6 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0010 | 0/0 | 5385 | 6 | 1 | 1 | 0 | 1 | 3 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0011 | 0/0 | 5386 | 6 | 0 | 3 | 1 | 0 | 2 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5381): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0012 | 0/0 | 5385 | 6 | 0 | 0 | 6 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0013 | 0/0 | 5385 | 5 | 0 | 0 | 5 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0014 | 0/0 | 5385 | 4 | 4 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0015 | 0/0 | 5385 | 3 | 3 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0016 | 0/0 | 5380 | 3 | 0 | 0 | 0 | 0 | 3 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5375): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0017 | 0/0 | 5385 | 3 | 0 | 2 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0018 | 0/0 | 5385 | 3 | 0 | 0 | 3 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0019 | 0/0 | 5385 | 3 | 0 | 0 | 3 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0020 | 0/0 | 5385 | 2 | 2 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0021 | 0/0 | 5385 | 2 | 0 | 0 | 2 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0022 | 0/0 | 5385 | 2 | 1 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCT others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0023 | 0/0 | 5385 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0024 | 0/0 | 5385 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0025 | 0/0 | 5385 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0026 | 0/0 | 5386 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5381): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0027 | 0/0 | 5385 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0028 | 0/0 | 5385 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0029 | 0/0 | 5385 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0030 | 0/0 | 5385 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0031 | 0/0 | 5385 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0032 | 0/0 | 5386 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5381): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0033 | 0/0 | 5385 | 1 | 0 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0034 | 0/0 | 5385 | 1 | 0 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0035 | 0/0 | 5385 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0036 | 0/0 | 5385 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0037 | 0/0 | 5386 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5381): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0038 | 0/0 | 5385 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0039 | 0/0 | 5385 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0040 | 0/0 | 5385 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0041 | 0/0 | 5385 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0042 | 0/0 | 5385 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0043 | 0/0 | 5385 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0001c0001t0044 | 0/0 | 5385 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
a0002c0002t0003 | 0/0 | 5385 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | CTCCC others(5380): Show |
chr6 | 116566504 | 116602675 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 42 | 1 | 8 | 27 | 3 | 3 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0004 | 0/0 | 9 | 1 | 4 | 4 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0002 | 0/0 | 35 | 0 | 8 | 23 | 3 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0007 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0020 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0003 | 0/0 | 14 | 3 | 3 | 6 | 1 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0034 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0006 | 0/0 | 12 | 7 | 1 | 3 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0014 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0016 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0005g0005 | 0/0 | 14 | 4 | 1 | 9 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0006g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0006g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0007g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0007g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0008g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0009g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0009g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0010g0003 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0011g0018 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0012g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0013g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0014g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0015g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0016g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0016g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0017g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0017g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0018g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0018g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0019g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0020g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0021g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0022g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0022g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0023g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0024g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0025g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0026g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0027g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0028g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0029g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0030g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0031g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0032g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0033g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0034g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0035g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0036g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0037g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0038g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0039g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0040g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0041g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0042g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0043g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0001c0001t0044g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
a0002c0002t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0071 | EUR | FIN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00280 | hp2 | a0001 | c0001 | t0034 | g0131 | EUR | FIN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0034 | EUR | FIN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00323 | hp2 | a0001 | c0001 | t0033 | g0002 | EUR | FIN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00621 | hp2 | a0001 | c0001 | t0013 | g0004 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00639 | hp2 | a0001 | c0001 | t0022 | g0109 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00642 | hp2 | a0001 | c0001 | t0010 | g0003 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00673 | hp1 | a0001 | c0001 | t0018 | g0125 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | CHS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01074 | hp1 | a0001 | c0001 | t0030 | g0004 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0110 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01106 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01109 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0054 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01258 | hp2 | a0001 | c0001 | t0017 | g0044 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | IBS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | IBS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0107 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01981 | hp2 | a0001 | c0001 | t0032 | g0004 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02027 | hp1 | a0001 | c0001 | t0026 | g0019 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02055 | hp2 | a0001 | c0001 | t0015 | g0022 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02129 | hp2 | a0001 | c0001 | t0007 | g0050 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02132 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02148 | hp2 | a0001 | c0001 | t0017 | g0044 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02165 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | CDX | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02257 | hp1 | a0001 | c0001 | t0023 | g0003 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0003 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02273 | hp1 | a0001 | c0001 | t0029 | g0088 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02451 | hp1 | a0001 | c0001 | t0036 | g0053 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02451 | hp2 | a0001 | c0001 | t0020 | g0022 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02523 | hp1 | a0001 | c0001 | t0011 | g0112 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0089 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02615 | hp2 | a0001 | c0001 | t0027 | g0049 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02647 | hp2 | a0001 | c0001 | t0043 | g0115 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02717 | hp1 | a0001 | c0001 | t0044 | g0062 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02717 | hp2 | a0001 | c0001 | t0014 | g0015 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02723 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02735 | hp1 | a0001 | c0001 | t0017 | g0114 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02735 | hp2 | a0001 | c0001 | t0011 | g0113 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02818 | hp2 | a0001 | c0001 | t0015 | g0031 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02895 | hp1 | a0001 | c0001 | t0014 | g0015 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02896 | hp2 | a0001 | c0001 | t0015 | g0031 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02897 | hp2 | a0001 | c0001 | t0014 | g0015 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02976 | hp2 | a0001 | c0001 | t0042 | g0056 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03017 | hp1 | a0001 | c0001 | t0010 | g0035 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03017 | hp2 | a0001 | c0001 | t0035 | g0028 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0057 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03209 | hp1 | a0001 | c0001 | t0020 | g0022 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03209 | hp2 | a0001 | c0001 | t0022 | g0017 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03486 | hp2 | a0001 | c0001 | t0039 | g0017 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03490 | hp1 | a0001 | c0001 | t0010 | g0003 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03491 | hp2 | a0001 | c0001 | t0011 | g0018 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03492 | hp2 | a0001 | c0001 | t0010 | g0003 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03540 | hp2 | a0001 | c0001 | t0014 | g0015 | AFR | GWD | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03654 | hp2 | a0001 | c0001 | t0007 | g0030 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03688 | hp1 | a0001 | c0001 | t0016 | g0087 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0028 | SAS | BEB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03927 | hp1 | a0001 | c0001 | t0007 | g0030 | SAS | BEB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03927 | hp2 | a0001 | c0001 | t0025 | g0073 | SAS | BEB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03942 | hp1 | a0001 | c0001 | t0024 | g0035 | SAS | BEB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG04115 | hp1 | a0001 | c0001 | t0041 | g0002 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG04115 | hp2 | a0001 | c0001 | t0016 | g0039 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG04204 | hp1 | a0001 | c0001 | t0038 | g0002 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG04228 | hp1 | a0001 | c0001 | t0040 | g0006 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG04228 | hp2 | a0001 | c0001 | t0016 | g0039 | SAS | STU | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18612 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | CHB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | YRI | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | YRI | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18944 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18952 | hp1 | a0001 | c0001 | t0031 | g0004 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18956 | hp1 | a0001 | c0001 | t0019 | g0007 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18957 | hp2 | a0001 | c0001 | t0019 | g0007 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18964 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18968 | hp1 | a0001 | c0001 | t0012 | g0093 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18974 | hp1 | a0001 | c0001 | t0013 | g0004 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18982 | hp2 | a0001 | c0001 | t0018 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18988 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18989 | hp1 | a0001 | c0001 | t0013 | g0004 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19004 | hp1 | a0001 | c0001 | t0019 | g0007 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19007 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19009 | hp1 | a0001 | c0001 | t0013 | g0004 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | LWK | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | LWK | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | LWK | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | LWK | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19057 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19060 | hp1 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19060 | hp2 | a0001 | c0001 | t0018 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19063 | hp2 | a0001 | c0001 | t0021 | g0094 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19078 | hp2 | a0001 | c0001 | t0037 | g0007 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19080 | hp2 | a0001 | c0001 | t0013 | g0083 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19091 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | YRI | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ASW | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20752 | hp1 | a0001 | c0001 | t0010 | g0003 | EUR | TSI | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0068 | EUR | TSI | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | GIH | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0075 | SAS | GIH | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG01123 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | CLM | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0052 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0060 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | USA | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | USA | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | USA | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | USA | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | LWK | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
NA21309 | hp2 | a0001 | c0001 | t0028 | g0072 | AFR | LWK | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0079 | REF | REF | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0034 | REF | REF | RWDD1_chr6_116566504_116602675 | RWDD1 | chr6 | 116566504 | 116602675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116584772 | A | G | 1 | a0002 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.185A>G | p.Asp62Gly | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/7 | 264/5385 | 185/732 | 62/243 | chr6 | 116584772 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116571508 | C | T | 1 | a0001c0001t0022 | 2 | HG00639.hp2 HG03209.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-75C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/7 | chr6 | 116571508 | |||||||
chr6:116571518 | G | C | 4 | a0001c0001t0010 a0001c0001t0023 a0001c0001t0024 others(1): Show |
9 | HG00642.hp2 HG02257.hp1 HG02258.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-65G>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/7 | 65 | chr6 | 116571518 | ||||||
chr6:116571571 | G | A | 1 | a0001c0001t0011 | 6 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-12G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/7 | 12 | chr6 | 116571571 | ||||||
chr6:116571579 | C | T | 1 | a0001c0001t0044 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-4C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/7 | 4 | chr6 | 116571579 | ||||||
chr6:116593223 | A | G | 1 | a0001c0001t0021 | 2 | NA19060.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*122A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 122 | chr6 | 116593223 | ||||||
chr6:116593384 | G | T | 1 | a0001c0001t0043 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283G>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 283 | chr6 | 116593384 | ||||||
chr6:116593667 | C | T | 2 | a0001c0001t0041 a0001c0001t0042 |
2 | HG02976.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*566C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 566 | chr6 | 116593667 | ||||||
chr6:116593757 | A | G | 4 | a0001c0001t0004 a0001c0001t0022 a0001c0001t0039 others(1): Show |
43 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*656A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 656 | chr6 | 116593757 | ||||||
chr6:116593773 | G | A | 1 | a0001c0001t0014 | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*672G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 672 | chr6 | 116593773 | ||||||
chr6:116593788 | A | G | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(34): Show |
317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*687A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 687 | chr6 | 116593788 | ||||||
chr6:116593855 | C | G | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(33): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*754C>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 754 | chr6 | 116593855 | ||||||
chr6:116593901 | C | T | 1 | a0001c0001t0038 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*800C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 800 | chr6 | 116593901 | ||||||
chr6:116593903 | C | G | 1 | a0001c0001t0027 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802C>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 802 | chr6 | 116593903 | ||||||
chr6:116593923 | C | T | 1 | a0001c0001t0040 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*822C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 822 | chr6 | 116593923 | ||||||
chr6:116593924 | A | G | 23 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(20): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*823A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 823 | chr6 | 116593924 | ||||||
chr6:116593967 | T | G | 1 | a0001c0001t0029 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*866T>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 866 | chr6 | 116593967 | ||||||
chr6:116594063 | G | A | 2 | a0001c0001t0015 a0001c0001t0020 |
5 | HG02055.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*962G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 962 | chr6 | 116594063 | ||||||
chr6:116594116 | C | CT | 5 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0026 others(2): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1030dupT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 1031 | INFO_REALIGN_3_PRIME | chr6 | 116594116 | |||||
chr6:116594211 | A | G | 1 | a0001c0001t0009 | 7 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1110A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 1110 | chr6 | 116594211 | ||||||
chr6:116594226 | C | T | 4 | a0001c0001t0004 a0001c0001t0022 a0001c0001t0039 others(1): Show |
43 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1125C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 1125 | chr6 | 116594226 | ||||||
chr6:116594904 | A | G | 1 | a0001c0001t0013 | 5 | HG00621.hp2 NA18974.hp1 NA18989.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1803A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 1803 | chr6 | 116594904 | ||||||
chr6:116594928 | T | C | 1 | a0001c0001t0023 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1827T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 1827 | chr6 | 116594928 | ||||||
chr6:116594970 | C | T | 3 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0036 |
12 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1869C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 1869 | chr6 | 116594970 | ||||||
chr6:116595035 | G | T | 1 | a0001c0001t0008 | 8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1934G>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 1934 | chr6 | 116595035 | ||||||
chr6:116595118 | A | G | 3 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0020 |
15 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2017A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2017 | chr6 | 116595118 | ||||||
chr6:116595150 | A | G | 1 | a0001c0001t0019 | 3 | NA18956.hp1 NA18957.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2049A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2049 | chr6 | 116595150 | ||||||
chr6:116595290 | C | T | 2 | a0001c0001t0007 a0001c0001t0035 |
11 | HG02129.hp2 HG02572.hp2 HG02886.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2189C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2189 | chr6 | 116595290 | ||||||
chr6:116595336 | C | T | 1 | a0001c0001t0020 | 2 | HG02451.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2235C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2235 | chr6 | 116595336 | ||||||
chr6:116595355 | C | A | 1 | a0001c0001t0024 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2254C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2254 | chr6 | 116595355 | ||||||
chr6:116595492 | C | T | 1 | a0001c0001t0034 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2391C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2391 | chr6 | 116595492 | ||||||
chr6:116595543 | CTTTGA | C | 1 | a0001c0001t0016 | 3 | HG03688.hp1 HG04115.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2447_*2451delATTT others(1): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2447 | INFO_REALIGN_3_PRIME | chr6 | 116595543 | |||||
chr6:116595566 | T | A | 3 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0017 |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2465T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2465 | chr6 | 116595566 | ||||||
chr6:116595860 | G | A | 1 | a0001c0001t0043 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2759G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2759 | chr6 | 116595860 | ||||||
chr6:116595967 | A | C | 1 | a0001c0001t0031 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2866A>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2866 | chr6 | 116595967 | ||||||
chr6:116596032 | G | A | 1 | a0001c0001t0039 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2931G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 2931 | chr6 | 116596032 | ||||||
chr6:116596270 | C | T | 3 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0017 |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3169C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 3169 | chr6 | 116596270 | ||||||
chr6:116596904 | T | C | 1 | a0001c0001t0030 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3803T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 3803 | chr6 | 116596904 | ||||||
chr6:116596932 | C | T | 1 | a0001c0001t0017 | 3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3831C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 3831 | chr6 | 116596932 | ||||||
chr6:116596987 | A | G | 1 | a0001c0001t0005 | 19 | HG00544.hp2 HG01106.hp1 HG02132.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3886A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 3886 | chr6 | 116596987 | ||||||
chr6:116597154 | G | C | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(17): Show |
162 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*4053G>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 4053 | chr6 | 116597154 | ||||||
chr6:116597191 | T | C | 1 | a0001c0001t0035 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4090T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 4090 | chr6 | 116597191 | ||||||
chr6:116597312 | A | G | 1 | a0001c0001t0033 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4211A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 4211 | chr6 | 116597312 | ||||||
chr6:116597397 | C | T | 2 | a0001c0001t0009 a0001c0001t0036 |
8 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4296C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 4296 | chr6 | 116597397 | ||||||
chr6:116597448 | G | A | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(33): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*4347G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 4347 | chr6 | 116597448 | ||||||
chr6:116597636 | T | A | 8 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0025 others(5): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*4535T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 4535 | chr6 | 116597636 | ||||||
chr6:116597637 | A | T | 3 | a0001c0001t0012 a0001c0001t0021 a0001c0001t0029 |
9 | HG02273.hp1 NA18944.hp2 NA18968.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4536A>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 7/7 | 4536 | chr6 | 116597637 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116571676 | C | T | 43 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(40): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.73+21C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116571676 | |||||||
chr6:116571790 | C | CTT | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.73+135_73+136insTT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116571790 | |||||||
chr6:116571802 | C | T | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.73+147C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116571802 | |||||||
chr6:116571924 | T | C | 1 | a0001c0001t0027g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.73+269T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116571924 | |||||||
chr6:116571983 | C | A | 68 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(65): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.73+328C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116571983 | |||||||
chr6:116572008 | A | G | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.73+353A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116572008 | |||||||
chr6:116572163 | GA | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(106): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.73+521delA | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116572163 | ||||||
chr6:116572301 | C | T | 67 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(64): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.73+646C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116572301 | |||||||
chr6:116572320 | G | A | 2 | a0001c0001t0003g0051 a0001c0001t0014g0015 |
5 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.73+665G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116572320 | |||||||
chr6:116572361 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0108 |
3 | HG01258.hp1 HG01515.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.73+706A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116572361 | |||||||
chr6:116572403 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.73+748C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116572403 | |||||||
chr6:116572586 | A | C | 38 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(35): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.73+931A>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116572586 | |||||||
chr6:116572606 | C | T | 5 | a0001c0001t0004g0017 a0001c0001t0004g0110 a0001c0001t0022g0017 others(2): Show |
6 | HG00639.hp2 HG01074.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+951C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116572606 | |||||||
chr6:116572925 | T | A | 1 | a0001c0001t0042g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.73+1270T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116572925 | |||||||
chr6:116572952 | G | A | 1 | a0001c0001t0009g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73+1297G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116572952 | |||||||
chr6:116573025 | C | T | 1 | a0001c0001t0028g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73+1370C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116573025 | |||||||
chr6:116573053 | T | C | 5 | a0001c0001t0002g0025 a0001c0001t0002g0045 a0001c0001t0002g0117 others(2): Show |
8 | HG00609.hp2 HG02040.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.73+1398T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116573053 | |||||||
chr6:116573231 | A | T | 1 | a0001c0001t0015g0031 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.73+1576A>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116573231 | |||||||
chr6:116573407 | T | G | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.73+1752T>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116573407 | |||||||
chr6:116573697 | AAG | A | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.73+2046_73+2047del others(2): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116573697 | ||||||
chr6:116573698 | A | G | 5 | a0001c0001t0009g0011 a0001c0001t0009g0052 a0001c0001t0009g0054 others(2): Show |
12 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.73+2043A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116573698 | |||||||
chr6:116573823 | C | CT | 37 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(34): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.73+2179dupT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116573823 | ||||||
chr6:116573837 | T | C | 1 | a0001c0001t0013g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.73+2182T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116573837 | |||||||
chr6:116573865 | A | G | 1 | a0001c0001t0004g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.73+2210A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116573865 | |||||||
chr6:116574268 | C | T | 1 | a0001c0001t0043g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.73+2613C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116574268 | |||||||
chr6:116574363 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.73+2708G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116574363 | |||||||
chr6:116574396 | G | A | 1 | a0001c0001t0016g0039 | 2 | HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.73+2741G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116574396 | |||||||
chr6:116574399 | C | T | 81 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(78): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.73+2744C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116574399 | |||||||
chr6:116574647 | A | ACTTTCTT others(5): Show |
2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.73+3003_73+3014dup others(12): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116574647 | ||||||
chr6:116574647 | ACTTT | A | 53 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(50): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.73+3011_73+3014del others(4): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116574647 | ||||||
chr6:116574662 | TTCTTTCT others(1): Show |
T | 21 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0016 others(18): Show |
43 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.73+3011_73+3018del others(8): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116574662 | ||||||
chr6:116574748 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.73+3093T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116574748 | |||||||
chr6:116574839 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73+3184G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116574839 | |||||||
chr6:116574893 | A | G | 1 | a0001c0001t0006g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73+3238A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116574893 | |||||||
chr6:116574922 | C | T | 1 | a0001c0001t0015g0031 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.73+3267C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116574922 | |||||||
chr6:116575019 | C | A | 1 | a0001c0001t0043g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.73+3364C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575019 | |||||||
chr6:116575049 | C | T | 1 | a0001c0001t0007g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73+3394C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575049 | |||||||
chr6:116575080 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73+3425C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575080 | |||||||
chr6:116575095 | A | AT | 3 | a0001c0001t0009g0011 a0001c0001t0009g0052 a0001c0001t0009g0054 |
7 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+3449dupT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116575095 | ||||||
chr6:116575095 | A | T | 1 | a0001c0001t0007g0030 | 2 | HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.73+3440A>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575095 | |||||||
chr6:116575096 | T | A | 2 | a0001c0001t0005g0086 a0001c0001t0028g0072 |
2 | NA19000.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.73+3441T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575096 | |||||||
chr6:116575125 | T | C | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.73+3470T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575125 | |||||||
chr6:116575322 | G | T | 1 | a0001c0001t0004g0110 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.73+3667G>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575322 | |||||||
chr6:116575365 | C | T | 3 | a0001c0001t0011g0018 a0001c0001t0011g0112 a0001c0001t0011g0113 |
6 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+3710C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575365 | |||||||
chr6:116575368 | G | A | 1 | a0001c0001t0016g0087 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.73+3713G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575368 | |||||||
chr6:116575565 | A | T | 38 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(35): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.73+3910A>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575565 | |||||||
chr6:116575572 | GC | G | 21 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0016 others(18): Show |
43 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.73+3920delC | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116575572 | ||||||
chr6:116575748 | C | T | 74 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(71): Show |
162 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.73+4093C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575748 | |||||||
chr6:116575799 | G | A | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.73+4144G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575799 | |||||||
chr6:116575902 | A | C | 1 | a0001c0001t0003g0074 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.73+4247A>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575902 | |||||||
chr6:116575992 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.74-4303A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116575992 | |||||||
chr6:116576032 | A | AT | 2 | a0001c0001t0001g0042 a0001c0001t0001g0106 |
3 | NA18939.hp2 NA18978.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.74-4262dupT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116576032 | ||||||
chr6:116576448 | G | A | 1 | a0001c0001t0028g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.74-3847G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116576448 | |||||||
chr6:116576567 | C | T | 1 | a0001c0001t0002g0136 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.74-3728C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116576567 | |||||||
chr6:116576636 | AT | A | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.74-3658delT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116576636 | |||||||
chr6:116577050 | G | T | 2 | a0001c0001t0003g0019 a0001c0001t0026g0019 |
4 | HG02027.hp1 HG02080.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.74-3245G>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577050 | |||||||
chr6:116577153 | A | G | 1 | a0001c0001t0003g0069 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.74-3142A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577153 | |||||||
chr6:116577159 | A | C | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.74-3136A>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577159 | |||||||
chr6:116577253 | A | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(128): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.74-3042A>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577253 | |||||||
chr6:116577460 | T | A | 1 | a0001c0001t0029g0088 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.74-2835T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577460 | |||||||
chr6:116577507 | G | GCATGTTC others(311): Show |
1 | a0001c0001t0002g0121 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.74-2772_74-2771ins others(318): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116577507 | ||||||
chr6:116577507 | G | GCATGTTC others(322): Show |
2 | a0001c0001t0002g0046 a0001c0001t0002g0122 |
3 | HG01516.hp1 HG01517.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.74-2772_74-2771ins others(329): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116577507 | ||||||
chr6:116577507 | G | GCATGTTC others(323): Show |
25 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0025 others(22): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.74-2772_74-2771ins others(330): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116577507 | ||||||
chr6:116577507 | G | GCATGTTC others(324): Show |
8 | a0001c0001t0002g0007 a0001c0001t0002g0045 a0001c0001t0002g0132 others(5): Show |
18 | HG00597.hp2 HG00639.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.74-2772_74-2771ins others(331): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116577507 | ||||||
chr6:116577507 | G | GCATGTTC others(325): Show |
1 | a0001c0001t0002g0119 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.74-2772_74-2771ins others(332): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116577507 | ||||||
chr6:116577593 | G | A | 1 | a0001c0001t0006g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.74-2702G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577593 | |||||||
chr6:116577651 | C | G | 74 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(71): Show |
162 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.74-2644C>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577651 | |||||||
chr6:116577678 | T | A | 8 | a0001c0001t0006g0012 a0001c0001t0006g0037 a0001c0001t0006g0067 others(5): Show |
15 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.74-2617T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577678 | |||||||
chr6:116577699 | C | T | 1 | a0001c0001t0034g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.74-2596C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577699 | |||||||
chr6:116577839 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.74-2456C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577839 | |||||||
chr6:116577907 | T | C | 5 | a0001c0001t0005g0005 a0001c0001t0005g0040 a0001c0001t0005g0086 others(2): Show |
19 | HG00544.hp2 HG01106.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.74-2388T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577907 | |||||||
chr6:116577914 | T | C | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.74-2381T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577914 | |||||||
chr6:116577923 | A | T | 38 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(35): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.74-2372A>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577923 | |||||||
chr6:116577934 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.74-2361T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116577934 | |||||||
chr6:116578097 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.74-2198A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116578097 | |||||||
chr6:116578159 | C | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(128): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.74-2136C>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116578159 | |||||||
chr6:116578315 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.74-1980A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116578315 | |||||||
chr6:116578530 | G | A | 3 | a0001c0001t0011g0018 a0001c0001t0011g0112 a0001c0001t0011g0113 |
6 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.74-1765G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116578530 | |||||||
chr6:116578555 | A | G | 2 | a0001c0001t0006g0037 a0001c0001t0006g0070 |
3 | HG02109.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.74-1740A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116578555 | |||||||
chr6:116578885 | C | CT | 74 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(71): Show |
162 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.74-1402dupT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 116578885 | ||||||
chr6:116579099 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.74-1196C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579099 | |||||||
chr6:116579104 | G | C | 5 | a0001c0001t0009g0011 a0001c0001t0009g0052 a0001c0001t0009g0054 others(2): Show |
12 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.74-1191G>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579104 | |||||||
chr6:116579119 | G | A | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.74-1176G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579119 | |||||||
chr6:116579123 | G | A | 1 | a0001c0001t0003g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.74-1172G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579123 | |||||||
chr6:116579146 | G | C | 1 | a0001c0001t0002g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.74-1149G>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579146 | |||||||
chr6:116579171 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.74-1124C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579171 | |||||||
chr6:116579379 | G | T | 2 | a0001c0001t0008g0008 a0001c0001t0008g0111 |
8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.74-916G>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579379 | |||||||
chr6:116579393 | C | T | 1 | a0001c0001t0007g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.74-902C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579393 | |||||||
chr6:116579407 | G | C | 5 | a0001c0001t0009g0011 a0001c0001t0009g0052 a0001c0001t0009g0054 others(2): Show |
12 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.74-888G>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579407 | |||||||
chr6:116579836 | C | T | 1 | a0001c0001t0002g0027 | 3 | NA18950.hp1 NA18968.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.74-459C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579836 | |||||||
chr6:116579837 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.74-458A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116579837 | |||||||
chr6:116580022 | C | A | 81 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(78): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.74-273C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116580022 | |||||||
chr6:116580152 | G | C | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
7 | HG02129.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-143G>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116580152 | |||||||
chr6:116580201 | C | T | 1 | a0001c0001t0005g0089 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.74-94C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 1/6 | chr6 | 116580201 | |||||||
chr6:116580440 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0091 |
3 | HG01516.hp2 HG01517.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.139+80T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116580440 | |||||||
chr6:116580445 | A | G | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.139+85A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116580445 | |||||||
chr6:116580477 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(128): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.139+117G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116580477 | |||||||
chr6:116580698 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.139+338T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116580698 | |||||||
chr6:116580767 | G | A | 1 | a0001c0001t0018g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.139+407G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116580767 | |||||||
chr6:116580830 | C | T | 1 | a0001c0001t0007g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.139+470C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116580830 | |||||||
chr6:116580970 | C | T | 37 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(34): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.139+610C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116580970 | |||||||
chr6:116581239 | A | G | 8 | a0001c0001t0006g0012 a0001c0001t0006g0037 a0001c0001t0006g0067 others(5): Show |
15 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.139+879A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116581239 | |||||||
chr6:116581302 | A | G | 1 | a0001c0001t0003g0036 | 2 | NA18947.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.139+942A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116581302 | |||||||
chr6:116581356 | T | C | 4 | a0001c0001t0007g0028 a0001c0001t0007g0030 a0001c0001t0007g0050 others(1): Show |
5 | HG02129.hp2 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.139+996T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116581356 | |||||||
chr6:116581382 | C | A | 3 | a0001c0001t0004g0016 a0001c0001t0004g0075 a0001c0001t0004g0076 |
6 | HG02602.hp2 HG03490.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.139+1022C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116581382 | |||||||
chr6:116581477 | C | T | 2 | a0001c0001t0010g0035 a0001c0001t0024g0035 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.139+1117C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116581477 | |||||||
chr6:116581481 | A | G | 1 | a0001c0001t0043g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.139+1121A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116581481 | |||||||
chr6:116581706 | T | C | 1 | a0001c0001t0036g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.139+1346T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116581706 | |||||||
chr6:116581828 | C | T | 8 | a0001c0001t0006g0012 a0001c0001t0006g0037 a0001c0001t0006g0067 others(5): Show |
15 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.139+1468C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116581828 | |||||||
chr6:116581950 | G | A | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.139+1590G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116581950 | |||||||
chr6:116582253 | GT | G | 25 | a0001c0001t0001g0092 a0001c0001t0002g0126 a0001c0001t0003g0032 others(22): Show |
42 | HG00738.hp1 HG01106.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.139+1907delT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 116582253 | ||||||
chr6:116582332 | A | G | 1 | a0001c0001t0017g0114 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.139+1972A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116582332 | |||||||
chr6:116582374 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.139+2014G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116582374 | |||||||
chr6:116582522 | A | G | 1 | a0001c0001t0036g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.139+2162A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116582522 | |||||||
chr6:116582531 | A | T | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.139+2171A>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116582531 | |||||||
chr6:116582723 | A | G | 37 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(34): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.140-2004A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116582723 | |||||||
chr6:116582781 | G | A | 37 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(34): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.140-1946G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116582781 | |||||||
chr6:116582922 | A | G | 1 | a0001c0001t0014g0015 | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-1805A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116582922 | |||||||
chr6:116582952 | CT | C | 83 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0108 others(80): Show |
178 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.140-1760delT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 116582952 | ||||||
chr6:116582952 | CTT | C | 4 | a0001c0001t0002g0020 a0001c0001t0002g0132 a0001c0001t0002g0133 others(1): Show |
7 | HG02145.hp2 HG02280.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.140-1761_140-1760d others(4): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 116582952 | ||||||
chr6:116582967 | T | A | 1 | a0001c0001t0007g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.140-1760T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116582967 | |||||||
chr6:116583305 | T | C | 4 | a0001c0001t0003g0009 a0001c0001t0003g0033 a0001c0001t0003g0063 others(1): Show |
10 | NA18939.hp1 NA18953.hp2 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.140-1422T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116583305 | |||||||
chr6:116583528 | C | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(2): Show |
14 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.140-1199C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116583528 | |||||||
chr6:116583533 | TACAC | T | 3 | a0001c0001t0011g0018 a0001c0001t0011g0112 a0001c0001t0011g0113 |
6 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.140-1178_140-1175d others(6): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 116583533 | ||||||
chr6:116583596 | A | G | 1 | a0001c0001t0001g0013 | 5 | HG03831.hp1 NA18943.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-1131A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116583596 | |||||||
chr6:116584004 | G | T | 2 | a0001c0001t0007g0057 a0001c0001t0007g0059 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.140-723G>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116584004 | |||||||
chr6:116584324 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(47): Show |
137 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.140-403A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116584324 | |||||||
chr6:116584387 | T | TA | 81 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(78): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.140-340_140-339ins others(1): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116584387 | |||||||
chr6:116584478 | G | A | 21 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0016 others(18): Show |
43 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.140-249G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116584478 | |||||||
chr6:116584649 | A | G | 1 | a0001c0001t0002g0124 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.140-78A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116584649 | |||||||
chr6:116584671 | A | G | 1 | a0001c0001t0003g0063 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.140-56A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 2/6 | chr6 | 116584671 | |||||||
chr6:116585008 | G | A | 1 | a0001c0001t0042g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.270+151G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585008 | |||||||
chr6:116585122 | C | T | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.270+265C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585122 | |||||||
chr6:116585171 | T | G | 1 | a0001c0001t0001g0096 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.270+314T>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585171 | |||||||
chr6:116585204 | T | A | 1 | a0001c0001t0002g0122 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.270+347T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585204 | |||||||
chr6:116585263 | GA | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(38): Show |
121 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.270+410delA | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 116585263 | ||||||
chr6:116585404 | T | G | 14 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0016 others(11): Show |
35 | HG00280.hp1 HG00741.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+547T>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585404 | |||||||
chr6:116585464 | T | A | 1 | a0001c0001t0002g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.270+607T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585464 | |||||||
chr6:116585479 | C | G | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.270+622C>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585479 | |||||||
chr6:116585588 | T | G | 1 | a0001c0001t0001g0097 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+731T>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585588 | |||||||
chr6:116585762 | A | G | 35 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0016 others(32): Show |
66 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.270+905A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585762 | |||||||
chr6:116585795 | T | C | 1 | a0001c0001t0004g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.270+938T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585795 | |||||||
chr6:116585917 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.270+1060C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585917 | |||||||
chr6:116585962 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.270+1105C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116585962 | |||||||
chr6:116586134 | C | A | 1 | a0001c0001t0002g0047 | 2 | NA18975.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.270+1277C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586134 | |||||||
chr6:116586134 | C | T | 1 | a0001c0001t0022g0109 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.270+1277C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586134 | |||||||
chr6:116586218 | A | C | 38 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(35): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.270+1361A>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586218 | |||||||
chr6:116586469 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.270+1612C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586469 | |||||||
chr6:116586529 | T | C | 1 | a0001c0001t0036g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.270+1672T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586529 | |||||||
chr6:116586541 | T | C | 1 | a0001c0001t0006g0067 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.270+1684T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586541 | |||||||
chr6:116586584 | A | G | 1 | a0001c0001t0002g0124 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.270+1727A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586584 | |||||||
chr6:116586620 | T | C | 2 | a0001c0001t0008g0008 a0001c0001t0008g0111 |
8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.270+1763T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586620 | |||||||
chr6:116586946 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.271-1896A>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586946 | |||||||
chr6:116586957 | T | C | 1 | a0001c0001t0002g0127 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.271-1885T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116586957 | |||||||
chr6:116587058 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.271-1784G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587058 | |||||||
chr6:116587104 | A | G | 21 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0016 others(18): Show |
43 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.271-1738A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587104 | |||||||
chr6:116587146 | A | G | 1 | a0001c0001t0002g0026 | 3 | HG02071.hp1 HG02129.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.271-1696A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587146 | |||||||
chr6:116587201 | G | T | 1 | a0001c0001t0004g0014 | 5 | HG00741.hp2 HG01255.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-1641G>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587201 | |||||||
chr6:116587367 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(154): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.271-1475G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587367 | |||||||
chr6:116587423 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(128): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.271-1419G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587423 | |||||||
chr6:116587601 | T | A | 1 | a0001c0001t0004g0078 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.271-1241T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587601 | |||||||
chr6:116587602 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(47): Show |
137 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.271-1240T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587602 | |||||||
chr6:116587662 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-1180C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587662 | |||||||
chr6:116587672 | A | ATG | 30 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0016 others(27): Show |
54 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.271-1152_271-1151d others(4): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 116587672 | ||||||
chr6:116587762 | AAGACC | A | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.271-1077_271-1073d others(7): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 116587762 | ||||||
chr6:116587778 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.271-1064T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587778 | |||||||
chr6:116587854 | G | A | 1 | a0001c0001t0004g0107 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.271-988G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116587854 | |||||||
chr6:116588239 | T | C | 1 | a0001c0001t0029g0088 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.271-603T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116588239 | |||||||
chr6:116588668 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.271-174G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116588668 | |||||||
chr6:116588680 | C | T | 5 | a0001c0001t0001g0101 a0001c0001t0009g0011 a0001c0001t0009g0052 others(2): Show |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.271-162C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 3/6 | chr6 | 116588680 | |||||||
chr6:116589070 | GT | G | 2 | a0001c0001t0008g0008 a0001c0001t0008g0111 |
8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+86delT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589070 | |||||||
chr6:116589075 | T | A | 1 | a0001c0001t0004g0038 | 2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.414+90T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589075 | |||||||
chr6:116589259 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.414+274G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589259 | |||||||
chr6:116589292 | GGAA | G | 7 | a0001c0001t0008g0008 a0001c0001t0008g0111 a0001c0001t0011g0018 others(4): Show |
17 | HG01106.hp2 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.414+317_414+319del others(3): Show |
RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 116589292 | ||||||
chr6:116589305 | T | C | 1 | a0001c0001t0003g0065 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.414+320T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589305 | |||||||
chr6:116589394 | G | A | 1 | a0001c0001t0025g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.414+409G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589394 | |||||||
chr6:116589520 | C | A | 2 | a0001c0001t0008g0008 a0001c0001t0008g0111 |
8 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+535C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589520 | |||||||
chr6:116589585 | T | G | 1 | a0001c0001t0002g0118 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.414+600T>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589585 | |||||||
chr6:116589691 | T | A | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.415-581T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589691 | |||||||
chr6:116589817 | T | A | 1 | a0001c0001t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.415-455T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589817 | |||||||
chr6:116589903 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.415-369C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116589903 | |||||||
chr6:116590102 | G | A | 81 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(78): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.415-170G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 4/6 | chr6 | 116590102 | |||||||
chr6:116590617 | A | G | 2 | a0001c0001t0007g0028 a0001c0001t0035g0028 |
2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.547+213A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 5/6 | chr6 | 116590617 | |||||||
chr6:116590849 | A | G | 1 | a0001c0001t0004g0080 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.548-39A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 5/6 | chr6 | 116590849 | |||||||
chr6:116590870 | C | CT | 9 | a0001c0001t0003g0021 a0001c0001t0003g0032 a0001c0001t0003g0064 others(6): Show |
14 | HG00741.hp1 HG01243.hp1 HG02055.hp2 others(11): Show |
splice_acceptor_variant&intron_variant | HIGH | c.548-3dupT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 116590870 | ||||||
chr6:116590870 | CT | C | 41 | a0001c0001t0001g0023 a0001c0001t0002g0002 a0001c0001t0002g0007 others(38): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
splice_region_variant&intron_variant | LOW | c.548-3delT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 116590870 | ||||||
chr6:116591108 | A | G | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.610+158A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116591108 | |||||||
chr6:116591278 | C | A | 6 | a0001c0001t0004g0017 a0001c0001t0004g0081 a0001c0001t0004g0110 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+328C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116591278 | |||||||
chr6:116591503 | C | G | 1 | a0001c0001t0005g0040 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.610+553C>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116591503 | |||||||
chr6:116591534 | G | C | 1 | a0001c0001t0003g0033 | 2 | NA18939.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.610+584G>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116591534 | |||||||
chr6:116591572 | A | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(128): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.610+622A>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116591572 | |||||||
chr6:116591628 | C | T | 1 | a0001c0001t0011g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.610+678C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116591628 | |||||||
chr6:116591674 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(38): Show |
121 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.610+724C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116591674 | |||||||
chr6:116591868 | T | C | 1 | a0001c0001t0004g0076 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.610+918T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116591868 | |||||||
chr6:116592056 | C | T | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.611-924C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592056 | |||||||
chr6:116592059 | T | A | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.611-921T>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592059 | |||||||
chr6:116592072 | G | A | 2 | a0001c0001t0017g0044 a0001c0001t0017g0114 |
3 | HG01258.hp2 HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.611-908G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592072 | |||||||
chr6:116592094 | A | G | 4 | a0001c0001t0007g0028 a0001c0001t0007g0030 a0001c0001t0007g0050 others(1): Show |
5 | HG02129.hp2 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.611-886A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592094 | |||||||
chr6:116592205 | A | AT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(38): Show |
121 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.611-769dupT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 116592205 | ||||||
chr6:116592254 | T | C | 21 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0016 others(18): Show |
43 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.611-726T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592254 | |||||||
chr6:116592380 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
30 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.611-600T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592380 | |||||||
chr6:116592435 | A | G | 1 | a0001c0001t0002g0133 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.611-545A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592435 | |||||||
chr6:116592508 | G | A | 37 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(34): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.611-472G>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592508 | |||||||
chr6:116592542 | C | A | 1 | a0001c0001t0002g0048 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.611-438C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592542 | |||||||
chr6:116592559 | T | C | 1 | a0001c0001t0008g0111 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.611-421T>C | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592559 | |||||||
chr6:116592601 | C | T | 1 | a0001c0001t0043g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.611-379C>T | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592601 | |||||||
chr6:116592679 | A | G | 5 | a0001c0001t0007g0028 a0001c0001t0007g0029 a0001c0001t0007g0030 others(2): Show |
7 | HG02129.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.611-301A>G | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592679 | |||||||
chr6:116592819 | C | A | 1 | a0001c0001t0002g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.611-161C>A | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | chr6 | 116592819 | |||||||
chr6:116592949 | A | AT | 21 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0016 others(18): Show |
43 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.611-16dupT | RWDD1 | ENSG00000111832.13 | transcript | ENST00000466444.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 116592949 |