Item | Value |
---|---|
geneid | 192670 |
ensemblid | ENSG00000134698.11 |
hgncid | 18424 |
symbol | AGO4 |
name | argonaute RISC component 4 |
refseq_nuc | NM_017629.4 |
refseq_prot | NP_060099.2 |
ensembl_nuc | ENST00000373210.4 |
ensembl_prot | ENSP00000362306.3 |
mane_status | MANE Select |
chr | chr1 |
start | 35808016 |
end | 35857890 |
strand | + |
ver | v1.2 |
region | chr1:35808016-35857890 |
region5000 | chr1:35803016-35862890 |
regionname0 | AGO4_chr1_35808016_35857890 |
regionname5000 | AGO4_chr1_35803016_35862890 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 861 | 269 | 92 | 42 | 101 | 10 | 22 | 83 | AGO4_chr1_35803016_35862890 | AGO4 | MEALG others(856): Show |
chr1 | 35803016 | 35862890 |
a0002 | 0/0 | 861 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | MEALG others(856): Show |
chr1 | 35803016 | 35862890 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2583 | 176 | 75 | 26 | 59 | 3 | 11 | AGO4_chr1_35803016_35862890 | AGO4 | ATGGA others(2578): Show |
chr1 | 35803016 | 35862890 | ||
a0001c0002 | 0/0 | 2583 | 86 | 10 | 16 | 42 | 7 | 11 | AGO4_chr1_35803016_35862890 | AGO4 | ATGGA others(2578): Show |
chr1 | 35803016 | 35862890 | ||
a0001c0003 | 0/0 | 2583 | 6 | 6 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | ATGGA others(2578): Show |
chr1 | 35803016 | 35862890 | ||
a0001c0005 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | ATGGA others(2578): Show |
chr1 | 35803016 | 35862890 | ||
a0002c0004 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | ATGGA others(2578): Show |
chr1 | 35803016 | 35862890 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7272 | 21 | 17 | 3 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0002 | 0/0 | 7275 | 75 | 10 | 13 | 47 | 1 | 4 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7270): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0003 | 0/0 | 7271 | 28 | 18 | 3 | 5 | 0 | 2 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0004 | 0/0 | 7271 | 8 | 2 | 0 | 0 | 2 | 4 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0005 | 0/0 | 7271 | 6 | 6 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0006 | 0/0 | 7270 | 6 | 3 | 0 | 2 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7265): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0007 | 0/0 | 7280 | 4 | 4 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7275): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0008 | 0/0 | 7273 | 2 | 1 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7268): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0009 | 0/0 | 7272 | 4 | 2 | 2 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0010 | 0/0 | 7274 | 3 | 1 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7269): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0011 | 0/0 | 7274 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7269): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0012 | 0/0 | 7274 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7269): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0015 | 0/0 | 7272 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0016 | 0/0 | 7271 | 2 | 0 | 2 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0018 | 0/0 | 7275 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7270): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0019 | 0/0 | 7276 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7271): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0021 | 0/0 | 7273 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7268): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0023 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0025 | 0/0 | 7272 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0027 | 0/0 | 7272 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0030 | 0/1 | 7269 | 1 | 0 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7264): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0031 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0032 | 0/0 | 7271 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0033 | 0/0 | 7272 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0001t0034 | 0/0 | 7270 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7265): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0001 | 0/0 | 7272 | 66 | 9 | 12 | 32 | 7 | 6 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0004 | 0/0 | 7271 | 3 | 0 | 0 | 3 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0005 | 0/0 | 7271 | 6 | 0 | 1 | 1 | 0 | 4 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0008 | 0/0 | 7273 | 2 | 1 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7268): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0014 | 0/0 | 7272 | 2 | 0 | 2 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0017 | 0/0 | 7281 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7276): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0020 | 0/0 | 7272 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0022 | 0/0 | 7272 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0024 | 0/0 | 7272 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0026 | 0/0 | 7272 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0028 | 0/0 | 7272 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0002t0029 | 0/0 | 7272 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0003t0001 | 0/0 | 7272 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7267): Show |
chr1 | 35803016 | 35862890 |
a0001c0003t0004 | 0/0 | 7271 | 3 | 3 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0001c0003t0013 | 0/0 | 7270 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7265): Show |
chr1 | 35803016 | 35862890 |
a0001c0005t0004 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7266): Show |
chr1 | 35803016 | 35862890 |
a0002c0004t0002 | 0/0 | 7275 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | GTTCC others(7270): Show |
chr1 | 35803016 | 35862890 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0001g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0008g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0009g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0010g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0010g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0011g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0012g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0015g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0015g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0016g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0016g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0018g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0019g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0021g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0023g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0025g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0027g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0030g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0031g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0032g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0033g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0001t0034g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0008g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0014g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0014g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0017g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0020g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0022g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0024g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0026g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0028g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0002t0029g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0003t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0001c0005t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
a0002c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0001 | g0178 | EUR | GBR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0194 | EUR | FIN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0013 | EUR | FIN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0188 | EUR | FIN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0013 | EUR | FIN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00438 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00438 | hp2 | a0001 | c0001 | t0010 | g0105 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00673 | hp1 | a0001 | c0001 | t0010 | g0014 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00673 | hp2 | a0001 | c0002 | t0005 | g0228 | EAS | CHS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0056 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0057 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01168 | hp1 | a0001 | c0001 | t0016 | g0249 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01168 | hp2 | a0001 | c0002 | t0014 | g0189 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01169 | hp1 | a0001 | c0001 | t0016 | g0247 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01175 | hp1 | a0001 | c0002 | t0005 | g0174 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0169 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01255 | hp2 | a0001 | c0001 | t0021 | g0248 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01433 | hp2 | a0001 | c0002 | t0014 | g0193 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0167 | EUR | IBS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0207 | EUR | IBS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0206 | EUR | IBS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0214 | EUR | IBS | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01891 | hp2 | a0001 | c0003 | t0004 | g0154 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01928 | hp2 | a0001 | c0001 | t0019 | g0095 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01943 | hp2 | a0001 | c0002 | t0020 | g0165 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02055 | hp2 | a0001 | c0003 | t0013 | g0153 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02056 | hp2 | a0001 | c0001 | t0018 | g0126 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02129 | hp2 | a0001 | c0001 | t0027 | g0070 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0073 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | CDX | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | CDX | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0055 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0181 | AMR | PEL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0058 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0243 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0140 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02717 | hp2 | a0001 | c0005 | t0004 | g0068 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02818 | hp1 | a0001 | c0001 | t0015 | g0072 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02886 | hp1 | a0001 | c0003 | t0013 | g0155 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02922 | hp1 | a0001 | c0003 | t0004 | g0156 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02970 | hp1 | a0001 | c0001 | t0012 | g0151 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03017 | hp1 | a0001 | c0002 | t0028 | g0202 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0250 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03098 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0245 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0253 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0187 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03516 | hp1 | a0001 | c0002 | t0008 | g0185 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03516 | hp2 | a0001 | c0003 | t0004 | g0152 | AFR | ESN | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03654 | hp1 | a0001 | c0002 | t0005 | g0237 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03654 | hp2 | a0001 | c0002 | t0005 | g0159 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0222 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0251 | SAS | PJL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0232 | SAS | BEB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03927 | hp1 | a0001 | c0002 | t0005 | g0205 | SAS | BEB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | BEB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG04199 | hp1 | a0001 | c0002 | t0005 | g0234 | SAS | STU | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0021 | SAS | STU | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18941 | hp1 | a0001 | c0002 | t0004 | g0183 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18960 | hp1 | a0001 | c0002 | t0024 | g0009 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18978 | hp2 | a0001 | c0002 | t0029 | g0227 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18982 | hp2 | a0001 | c0002 | t0004 | g0162 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18989 | hp2 | a0001 | c0002 | t0017 | g0203 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18991 | hp1 | a0001 | c0002 | t0026 | g0168 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18995 | hp2 | a0001 | c0001 | t0032 | g0035 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19060 | hp1 | a0001 | c0002 | t0022 | g0217 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19062 | hp1 | a0001 | c0002 | t0004 | g0164 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19063 | hp1 | a0002 | c0004 | t0002 | g0094 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19066 | hp1 | a0001 | c0002 | t0008 | g0213 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA19240 | hp2 | a0001 | c0001 | t0033 | g0172 | AFR | YRI | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ASW | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0252 | SAS | GIH | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | GIH | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02109 | hp2 | a0001 | c0001 | t0023 | g0143 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03471 | hp1 | a0001 | c0001 | t0034 | g0069 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | MSL | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG06807 | hp1 | a0001 | c0001 | t0025 | g0071 | AFR | USA | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
HG06807 | hp2 | a0001 | c0001 | t0031 | g0053 | AFR | USA | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | USA | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | USA | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | LWK | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
homoSapiens | chm13v2 | a0001 | c0001 | t0030 | g0049 | REF | REF | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0246 | REF | REF | AGO4_chr1_35803016_35862890 | AGO4 | chr1 | 35803016 | 35862890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:35834036 | C | T | 1 | a0002 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.1426C>T | p.Pro476Ser | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/18 | 1827/7272 | 1426/2586 | 476/861 | chr1 | 35834036 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:35825688 | A | G | 1 | a0001c0005 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.498A>G | p.Pro166Pro | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 5/18 | 899/7272 | 498/2586 | 166/861 | chr1 | 35825688 | |||
chr1:35841300 | C | T | 1 | a0001c0003 | 6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.1860C>T | p.Thr620Thr | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 14/18 | 2261/7272 | 1860/2586 | 620/861 | chr1 | 35841300 | |||
chr1:35850970 | A | C | 1 | a0001c0002 | 86 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(83): Show |
synonymous_variant | LOW | c.2394A>C | p.Ser798Ser | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/18 | 2795/7272 | 2394/2586 | 798/861 | chr1 | 35850970 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:35808170 | T | TGGC | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0018 others(2): Show |
81 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(78): Show |
5_prime_UTR_variant | MODIFIER | c.-223_-221dupCGG | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/18 | 220 | INFO_REALIGN_3_PRIME | chr1 | 35808170 | |||||
chr1:35808170 | T | TGGCGGCG others(2): Show |
2 | a0001c0001t0007 a0001c0002t0017 |
5 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-229_-221dupCGGCGG others(3): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/18 | 220 | INFO_REALIGN_3_PRIME | chr1 | 35808170 | |||||
chr1:35853672 | C | T | 1 | a0001c0001t0034 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*67C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 67 | chr1 | 35853672 | ||||||
chr1:35854402 | A | G | 1 | a0001c0001t0016 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*797A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 797 | chr1 | 35854402 | ||||||
chr1:35854484 | C | G | 1 | a0001c0001t0033 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 879 | chr1 | 35854484 | ||||||
chr1:35854557 | G | A | 1 | a0001c0002t0020 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*952G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 952 | chr1 | 35854557 | ||||||
chr1:35854592 | T | C | 1 | a0001c0001t0021 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*987T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 987 | chr1 | 35854592 | ||||||
chr1:35855300 | G | T | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(2): Show |
40 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1695G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1695 | chr1 | 35855300 | ||||||
chr1:35855375 | C | G | 1 | a0001c0002t0029 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1770C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1770 | chr1 | 35855375 | ||||||
chr1:35855466 | C | G | 1 | a0001c0002t0028 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1861C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1861 | chr1 | 35855466 | ||||||
chr1:35855513 | A | G | 1 | a0001c0001t0027 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1908A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1908 | chr1 | 35855513 | ||||||
chr1:35855547 | C | T | 1 | a0001c0001t0009 | 4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1942C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 1942 | chr1 | 35855547 | ||||||
chr1:35855652 | C | CT | 5 | a0001c0001t0008 a0001c0001t0018 a0001c0001t0019 others(2): Show |
7 | HG01243.hp1 HG01928.hp2 HG02056.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2065dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2066 | INFO_REALIGN_3_PRIME | chr1 | 35855652 | |||||
chr1:35855652 | CT | C | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(11): Show |
64 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2065delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2065 | INFO_REALIGN_3_PRIME | chr1 | 35855652 | |||||
chr1:35855694 | C | G | 1 | a0001c0001t0027 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2089C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2089 | chr1 | 35855694 | ||||||
chr1:35855720 | T | G | 1 | a0001c0002t0022 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2115T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2115 | chr1 | 35855720 | ||||||
chr1:35855748 | A | G | 1 | a0001c0001t0025 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2143 | chr1 | 35855748 | ||||||
chr1:35856022 | T | A | 3 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0021 |
5 | HG01255.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2417T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2417 | chr1 | 35856022 | ||||||
chr1:35856201 | G | A | 1 | a0001c0001t0034 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2596G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2596 | chr1 | 35856201 | ||||||
chr1:35856430 | G | T | 1 | a0001c0002t0024 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2825G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 2825 | chr1 | 35856430 | ||||||
chr1:35856830 | AG | A | 11 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0010 others(8): Show |
29 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3237delG | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3237 | INFO_REALIGN_3_PRIME | chr1 | 35856830 | |||||
chr1:35856836 | G | C | 2 | a0001c0001t0011 a0001c0002t0014 |
4 | HG01168.hp2 HG01433.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3231G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3231 | chr1 | 35856836 | ||||||
chr1:35856842 | G | A | 1 | a0001c0001t0021 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3237G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3237 | chr1 | 35856842 | ||||||
chr1:35856880 | A | G | 2 | a0001c0001t0015 a0001c0001t0025 |
3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3275A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3275 | chr1 | 35856880 | ||||||
chr1:35856906 | G | A | 1 | a0001c0001t0031 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3301G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3301 | chr1 | 35856906 | ||||||
chr1:35856936 | A | AACT | 3 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0021 |
5 | HG01255.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3333_*3335dupCTA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3336 | INFO_REALIGN_3_PRIME | chr1 | 35856936 | |||||
chr1:35857456 | C | T | 1 | a0001c0001t0023 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3851C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 3851 | chr1 | 35857456 | ||||||
chr1:35857727 | G | A | 1 | a0001c0001t0027 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4122G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 18/18 | 4122 | chr1 | 35857727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:35808459 | G | GCGGGACC others(7): Show |
1 | a0001c0001t0010g0014 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.19+36_19+49dupACCC others(10): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35808459 | ||||||
chr1:35808529 | G | A | 39 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0020 others(36): Show |
40 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.19+94G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35808529 | |||||||
chr1:35808651 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.19+216G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35808651 | |||||||
chr1:35808778 | C | G | 1 | a0001c0001t0012g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19+343C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35808778 | |||||||
chr1:35809023 | C | T | 8 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(5): Show |
9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+588C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809023 | |||||||
chr1:35809042 | T | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(245): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.19+607T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809042 | |||||||
chr1:35809275 | T | C | 4 | a0001c0001t0009g0055 a0001c0001t0009g0056 a0001c0001t0009g0057 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+840T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809275 | |||||||
chr1:35809511 | G | A | 115 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(112): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.19+1076G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809511 | |||||||
chr1:35809587 | A | G | 39 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0020 others(36): Show |
40 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.19+1152A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809587 | |||||||
chr1:35809783 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0005g0059 |
3 | HG02809.hp2 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.19+1348G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809783 | |||||||
chr1:35809790 | A | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | NA18944.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.19+1355A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809790 | |||||||
chr1:35809967 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.19+1532G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35809967 | |||||||
chr1:35810027 | C | CT | 23 | a0001c0001t0001g0005 a0001c0001t0001g0138 a0001c0001t0001g0139 others(20): Show |
25 | HG01109.hp1 HG01891.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.19+1604dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35810027 | ||||||
chr1:35810032 | T | G | 1 | a0001c0002t0005g0159 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.19+1597T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810032 | |||||||
chr1:35810036 | T | G | 95 | a0001c0001t0001g0173 a0001c0001t0002g0239 a0001c0001t0002g0240 others(92): Show |
99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.19+1601T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810036 | |||||||
chr1:35810036 | T | TG | 37 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0023 others(34): Show |
38 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.19+1601_19+1602ins others(1): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810036 | |||||||
chr1:35810037 | T | G | 1 | a0001c0001t0004g0061 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.19+1602T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810037 | |||||||
chr1:35810166 | G | T | 8 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(5): Show |
9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1731G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810166 | |||||||
chr1:35810303 | T | C | 1 | a0001c0001t0007g0016 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.19+1868T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810303 | |||||||
chr1:35810393 | C | T | 9 | a0001c0001t0011g0007 a0001c0001t0012g0151 a0001c0001t0012g0253 others(6): Show |
10 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+1958C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810393 | |||||||
chr1:35810438 | C | T | 5 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(2): Show |
5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+2003C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810438 | |||||||
chr1:35810601 | G | C | 2 | a0001c0002t0001g0008 a0001c0002t0001g0160 |
3 | HG01074.hp1 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.19+2166G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810601 | |||||||
chr1:35810798 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(85): Show |
95 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.19+2363C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810798 | |||||||
chr1:35810961 | G | A | 3 | a0001c0001t0007g0017 a0001c0001t0007g0018 a0001c0001t0007g0019 |
3 | HG02258.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.19+2526G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35810961 | |||||||
chr1:35810967 | A | ACTAAAAA others(16): Show |
1 | a0001c0002t0001g0161 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+2556_19+2578dup others(23): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35810967 | ||||||
chr1:35811083 | G | A | 2 | a0001c0001t0015g0072 a0001c0001t0025g0071 |
2 | HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.19+2648G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811083 | |||||||
chr1:35811150 | C | CA | 7 | a0001c0001t0002g0239 a0001c0001t0004g0062 a0001c0001t0015g0072 others(4): Show |
7 | HG01074.hp1 HG02145.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+2724dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35811150 | ||||||
chr1:35811150 | CA | C | 8 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(5): Show |
9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2724delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35811150 | ||||||
chr1:35811156 | A | C | 8 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(5): Show |
9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2721A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811156 | |||||||
chr1:35811160 | C | A | 1 | a0001c0001t0003g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.19+2725C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811160 | |||||||
chr1:35811290 | G | A | 3 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0242 |
3 | HG01069.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.19+2855G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811290 | |||||||
chr1:35811470 | C | A | 1 | a0001c0002t0001g0163 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.19+3035C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811470 | |||||||
chr1:35811470 | C | CA | 31 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(28): Show |
32 | HG01109.hp1 HG01169.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.19+3046dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35811470 | ||||||
chr1:35811548 | T | G | 1 | a0001c0001t0002g0077 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.19+3113T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811548 | |||||||
chr1:35811585 | G | A | 1 | a0001c0001t0006g0021 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19+3150G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811585 | |||||||
chr1:35811598 | C | T | 1 | a0001c0001t0011g0007 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.19+3163C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811598 | |||||||
chr1:35811599 | G | A | 1 | a0001c0001t0031g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19+3164G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811599 | |||||||
chr1:35811606 | G | T | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.19+3171G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811606 | |||||||
chr1:35811657 | G | A | 1 | a0001c0002t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.19+3222G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811657 | |||||||
chr1:35811727 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0002g0137 |
2 | NA18972.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.19+3292C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811727 | |||||||
chr1:35811746 | G | A | 1 | a0001c0001t0031g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19+3311G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811746 | |||||||
chr1:35811848 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.19+3413C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811848 | |||||||
chr1:35811987 | A | G | 1 | a0001c0002t0005g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.19+3552A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35811987 | |||||||
chr1:35812016 | G | A | 16 | a0001c0001t0002g0074 a0001c0001t0002g0078 a0001c0001t0002g0079 others(13): Show |
16 | HG00140.hp2 HG00558.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.19+3581G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35812016 | |||||||
chr1:35812057 | G | C | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19+3622G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35812057 | |||||||
chr1:35812209 | GA | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0023 others(29): Show |
33 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.19+3784delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35812209 | ||||||
chr1:35812559 | A | C | 1 | a0001c0002t0001g0236 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.19+4124A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35812559 | |||||||
chr1:35812886 | C | G | 1 | a0001c0001t0002g0135 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.20-3996C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35812886 | |||||||
chr1:35813266 | G | A | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.20-3616G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813266 | |||||||
chr1:35813281 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.20-3601C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813281 | |||||||
chr1:35813333 | C | T | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-3549C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813333 | |||||||
chr1:35813408 | C | CA | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-3460dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35813408 | ||||||
chr1:35813455 | T | G | 38 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0020 others(35): Show |
39 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.20-3427T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813455 | |||||||
chr1:35813582 | C | T | 2 | a0001c0001t0012g0151 a0001c0001t0012g0253 |
2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.20-3300C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813582 | |||||||
chr1:35813727 | C | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG01884.hp2 HG02717.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-3155C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813727 | |||||||
chr1:35813741 | C | G | 1 | a0001c0002t0005g0234 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.20-3141C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813741 | |||||||
chr1:35813778 | A | G | 3 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 |
3 | HG02922.hp2 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.20-3104A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813778 | |||||||
chr1:35813790 | AGAAGGAA others(4): Show |
A | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-3076_20-3066del others(11): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35813790 | ||||||
chr1:35813838 | G | A | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.20-3044G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35813838 | |||||||
chr1:35814007 | G | A | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.20-2875G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814007 | |||||||
chr1:35814037 | T | C | 27 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0060 others(24): Show |
31 | HG00438.hp2 HG00642.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.20-2845T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814037 | |||||||
chr1:35814074 | C | CA | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-2796dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35814074 | ||||||
chr1:35814147 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.20-2735A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814147 | |||||||
chr1:35814282 | A | G | 1 | a0001c0001t0012g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.20-2600A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814282 | |||||||
chr1:35814460 | C | G | 1 | a0001c0002t0001g0233 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.20-2422C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35814460 | |||||||
chr1:35815664 | T | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(245): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.20-1218T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815664 | |||||||
chr1:35815698 | A | T | 1 | a0001c0001t0006g0048 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.20-1184A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815698 | |||||||
chr1:35815735 | A | G | 107 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(104): Show |
116 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.20-1147A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815735 | |||||||
chr1:35815767 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.20-1115C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815767 | |||||||
chr1:35815781 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.20-1101C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35815781 | |||||||
chr1:35816216 | C | G | 1 | a0001c0002t0005g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.20-666C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816216 | |||||||
chr1:35816288 | T | C | 4 | a0001c0001t0009g0055 a0001c0001t0009g0056 a0001c0001t0009g0057 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-594T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816288 | |||||||
chr1:35816408 | G | A | 1 | a0001c0001t0031g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.20-474G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816408 | |||||||
chr1:35816798 | CAAAAAAA others(6): Show |
C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(82): Show |
92 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.20-73_20-61delAAAA others(9): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 35816798 | ||||||
chr1:35816812 | A | G | 1 | a0001c0002t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.20-70A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816812 | |||||||
chr1:35816816 | A | AG | 6 | a0001c0001t0001g0173 a0001c0001t0009g0055 a0001c0001t0033g0172 others(3): Show |
6 | HG01109.hp2 HG01169.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-66_20-65insG | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816816 | |||||||
chr1:35816816 | A | G | 88 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(85): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.20-66A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816816 | |||||||
chr1:35816818 | A | G | 31 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0024 others(28): Show |
32 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.20-64A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 1/17 | chr1 | 35816818 | |||||||
chr1:35817215 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.185+168C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817215 | |||||||
chr1:35817346 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.185+299G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817346 | |||||||
chr1:35817411 | G | GTA | 35 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(32): Show |
36 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.185+380_185+381dup others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35817411 | ||||||
chr1:35817429 | C | A | 1 | a0001c0001t0002g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.185+382C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817429 | |||||||
chr1:35817506 | G | A | 1 | a0001c0002t0001g0182 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.185+459G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817506 | |||||||
chr1:35817643 | G | C | 2 | a0001c0001t0015g0072 a0001c0001t0025g0071 |
2 | HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.185+596G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817643 | |||||||
chr1:35817784 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.185+737G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817784 | |||||||
chr1:35817844 | G | A | 1 | a0001c0002t0004g0183 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.185+797G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35817844 | |||||||
chr1:35818026 | A | G | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+979A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818026 | |||||||
chr1:35818067 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185+1020T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818067 | |||||||
chr1:35818151 | A | T | 1 | a0001c0001t0002g0077 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.185+1104A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818151 | |||||||
chr1:35818248 | T | C | 1 | a0001c0001t0006g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.185+1201T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818248 | |||||||
chr1:35818349 | C | T | 2 | a0001c0001t0002g0113 a0001c0002t0001g0175 |
2 | HG00642.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.185+1302C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818349 | |||||||
chr1:35818353 | A | G | 115 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(112): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.185+1306A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818353 | |||||||
chr1:35818625 | AAAAG | A | 47 | a0001c0001t0001g0063 a0001c0001t0001g0075 a0001c0001t0001g0139 others(44): Show |
53 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.185+1611_185+1614d others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818625 | ||||||
chr1:35818625 | AAAAGAAA others(1): Show |
A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0138 a0001c0001t0002g0092 others(9): Show |
13 | HG00642.hp1 HG00741.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+1607_185+1614d others(10): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818625 | ||||||
chr1:35818642 | A | AAAGG | 7 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(4): Show |
7 | HG01123.hp2 NA18944.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+1598_185+1599i others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818642 | ||||||
chr1:35818646 | A | G | 35 | a0001c0001t0001g0148 a0001c0001t0002g0006 a0001c0001t0002g0074 others(32): Show |
36 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.185+1599A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818646 | |||||||
chr1:35818646 | AAAGAAAG others(9): Show |
A | 1 | a0001c0005t0004g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.185+1607_185+1622d others(18): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818646 | ||||||
chr1:35818650 | A | AAAGG | 29 | a0001c0001t0002g0241 a0001c0001t0008g0169 a0001c0001t0009g0058 others(26): Show |
32 | HG01069.hp2 HG01243.hp1 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.185+1606_185+1607i others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818650 | ||||||
chr1:35818650 | A | G | 59 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0001g0141 others(56): Show |
65 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.185+1603A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818650 | |||||||
chr1:35818650 | AAAGAAAG others(5): Show |
A | 3 | a0001c0001t0002g0077 a0001c0001t0002g0133 a0001c0001t0004g0054 |
3 | HG03491.hp2 NA19074.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.185+1611_185+1622d others(14): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818650 | ||||||
chr1:35818654 | A | AAAGGAAG others(5): Show |
1 | a0001c0003t0004g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.185+1610_185+1611i others(14): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818654 | ||||||
chr1:35818654 | A | G | 120 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0065 others(117): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.185+1607A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818654 | |||||||
chr1:35818658 | A | AAAGAAAG others(141): Show |
1 | a0001c0001t0003g0024 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(150): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(197): Show |
1 | a0001c0001t0003g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(206): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(45): Show |
1 | a0001c0001t0003g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(54): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(53): Show |
1 | a0001c0001t0006g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(62): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(41): Show |
1 | a0001c0001t0003g0027 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(50): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(37): Show |
1 | a0001c0001t0003g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(46): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(37): Show |
1 | a0001c0001t0006g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(46): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(25): Show |
1 | a0001c0001t0007g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(34): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(21): Show |
1 | a0001c0001t0006g0021 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(30): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(25): Show |
1 | a0001c0001t0003g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(34): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(17): Show |
2 | a0001c0001t0003g0031 a0001c0001t0006g0048 |
2 | HG00438.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.185+1614_185+1615i others(26): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(21): Show |
1 | a0001c0001t0003g0032 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.185+1614_185+1615i others(30): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(25): Show |
2 | a0001c0001t0003g0033 a0001c0001t0003g0051 |
2 | NA18906.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.185+1614_185+1615i others(34): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(31): Show |
1 | a0001c0001t0006g0034 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(40): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(9): Show |
4 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0007g0016 others(1): Show |
4 | HG02145.hp1 HG02155.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+1614_185+1615i others(18): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(13): Show |
4 | a0001c0001t0003g0037 a0001c0001t0003g0047 a0001c0001t0003g0050 others(1): Show |
4 | HG00558.hp1 HG02922.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+1614_185+1615i others(22): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(17): Show |
7 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0023 others(4): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+1614_185+1615i others(26): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(21): Show |
7 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0044 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+1614_185+1615i others(30): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGAAAG others(25): Show |
1 | a0001c0001t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.185+1614_185+1615i others(34): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGGAAG others(1): Show |
10 | a0001c0001t0001g0173 a0001c0001t0021g0248 a0001c0002t0001g0182 others(7): Show |
10 | HG01123.hp1 HG01169.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+1618_185+1619i others(10): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGGAAG others(5): Show |
6 | a0001c0001t0009g0055 a0001c0002t0001g0215 a0001c0002t0001g0216 others(3): Show |
6 | HG01943.hp2 HG02155.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+1618_185+1619i others(14): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGGAAG others(9): Show |
1 | a0001c0002t0022g0217 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.185+1618_185+1619i others(18): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | AAAGGAAG others(13): Show |
1 | a0001c0002t0001g0166 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.185+1618_185+1619i others(22): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818658 | A | G | 121 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0001g0141 others(118): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.185+1611A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818658 | |||||||
chr1:35818658 | AAAGGAAG others(5): Show |
A | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG01884.hp2 HG01928.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+1619_185+1630d others(14): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818658 | ||||||
chr1:35818662 | G | A | 1 | a0001c0001t0005g0012 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.185+1615G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818662 | |||||||
chr1:35818662 | GAAGA | G | 19 | a0001c0001t0002g0242 a0001c0001t0004g0061 a0001c0002t0001g0167 others(16): Show |
19 | HG00140.hp1 HG00673.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.185+1619_185+1622d others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35818662 | ||||||
chr1:35818666 | A | G | 219 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(216): Show |
234 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.185+1619A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818666 | |||||||
chr1:35818674 | G | A | 1 | a0001c0005t0004g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.185+1627G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818674 | |||||||
chr1:35818811 | G | T | 1 | a0001c0002t0005g0228 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.185+1764G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35818811 | |||||||
chr1:35819416 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.185+2369C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35819416 | |||||||
chr1:35819451 | G | A | 1 | a0001c0002t0004g0164 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.185+2404G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35819451 | |||||||
chr1:35819457 | G | A | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+2410G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35819457 | |||||||
chr1:35819712 | G | A | 94 | a0001c0001t0001g0173 a0001c0001t0002g0239 a0001c0001t0002g0240 others(91): Show |
98 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.185+2665G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35819712 | |||||||
chr1:35819732 | C | CA | 171 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(168): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.185+2703dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35819732 | ||||||
chr1:35819732 | C | CAA | 12 | a0001c0001t0002g0093 a0001c0001t0002g0136 a0001c0001t0009g0056 others(9): Show |
12 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.185+2702_185+2703d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35819732 | ||||||
chr1:35819732 | CA | C | 20 | a0001c0001t0001g0067 a0001c0001t0004g0013 a0001c0001t0004g0054 others(17): Show |
22 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.185+2703delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35819732 | ||||||
chr1:35819799 | T | TA | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG01175.hp2 HG01884.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+2768dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35819799 | ||||||
chr1:35820004 | A | T | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2858A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820004 | |||||||
chr1:35820269 | A | T | 39 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0020 others(36): Show |
40 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.186-2593A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820269 | |||||||
chr1:35820337 | A | G | 1 | a0001c0002t0001g0214 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.186-2525A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820337 | |||||||
chr1:35820424 | C | T | 1 | a0001c0001t0031g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-2438C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820424 | |||||||
chr1:35820453 | G | A | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2409G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820453 | |||||||
chr1:35820701 | A | T | 1 | a0001c0002t0001g0209 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.186-2161A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820701 | |||||||
chr1:35820861 | G | A | 4 | a0001c0002t0001g0171 a0001c0002t0001g0178 a0001c0002t0001g0179 others(1): Show |
4 | HG00140.hp1 HG01109.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2001G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820861 | |||||||
chr1:35820937 | T | C | 1 | a0001c0001t0033g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.186-1925T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35820937 | |||||||
chr1:35821483 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-1379A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821483 | |||||||
chr1:35821511 | T | C | 1 | a0001c0001t0031g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-1351T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821511 | |||||||
chr1:35821520 | G | A | 1 | a0001c0001t0033g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.186-1342G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821520 | |||||||
chr1:35821819 | C | A | 1 | a0001c0001t0003g0030 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.186-1043C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821819 | |||||||
chr1:35821822 | A | T | 1 | a0001c0002t0008g0213 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.186-1040A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821822 | |||||||
chr1:35821893 | A | AT | 13 | a0001c0001t0002g0087 a0001c0001t0002g0136 a0001c0001t0004g0013 others(10): Show |
15 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-955dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35821893 | ||||||
chr1:35821950 | C | T | 38 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0020 others(35): Show |
39 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.186-912C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821950 | |||||||
chr1:35821997 | C | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(67): Show |
76 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.186-865C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35821997 | |||||||
chr1:35822072 | G | T | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.186-790G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822072 | |||||||
chr1:35822128 | C | T | 1 | a0001c0002t0004g0164 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.186-734C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822128 | |||||||
chr1:35822152 | T | C | 1 | a0001c0002t0001g0210 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-710T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822152 | |||||||
chr1:35822170 | A | G | 11 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(8): Show |
13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.186-692A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822170 | |||||||
chr1:35822261 | C | CT | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-593dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr1 | 35822261 | ||||||
chr1:35822351 | G | A | 69 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(66): Show |
75 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.186-511G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822351 | |||||||
chr1:35822533 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.186-329C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 2/17 | chr1 | 35822533 | |||||||
chr1:35823034 | G | A | 1 | a0001c0002t0001g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.306+52G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823034 | |||||||
chr1:35823164 | A | C | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.306+182A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823164 | |||||||
chr1:35823252 | A | AT | 12 | a0001c0001t0001g0149 a0001c0001t0002g0086 a0001c0001t0002g0132 others(9): Show |
12 | HG00140.hp2 HG01109.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.306+288dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 35823252 | ||||||
chr1:35823252 | AT | A | 6 | a0001c0001t0002g0081 a0001c0001t0002g0127 a0001c0001t0006g0022 others(3): Show |
6 | HG02451.hp2 HG03130.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+288delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 35823252 | ||||||
chr1:35823287 | CTG | C | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+307_306+308del others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 35823287 | ||||||
chr1:35823388 | G | T | 1 | a0001c0001t0002g0085 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.306+406G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823388 | |||||||
chr1:35823496 | G | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(85): Show |
95 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.306+514G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823496 | |||||||
chr1:35823528 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.306+546C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823528 | |||||||
chr1:35823571 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.306+589G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823571 | |||||||
chr1:35823755 | T | A | 129 | a0001c0001t0001g0173 a0001c0001t0002g0082 a0001c0001t0002g0088 others(126): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.306+773T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823755 | |||||||
chr1:35823758 | T | A | 1 | a0001c0001t0003g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.306+776T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823758 | |||||||
chr1:35823881 | C | T | 2 | a0001c0002t0001g0206 a0001c0002t0001g0207 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.306+899C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35823881 | |||||||
chr1:35824223 | C | T | 1 | a0001c0001t0008g0169 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.307-1090C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824223 | |||||||
chr1:35824280 | A | G | 5 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(2): Show |
5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-1033A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824280 | |||||||
chr1:35824448 | TA | T | 5 | a0001c0001t0002g0092 a0001c0001t0002g0099 a0001c0001t0002g0100 others(2): Show |
5 | NA18946.hp2 NA18973.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-864delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824448 | |||||||
chr1:35824537 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.307-776G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824537 | |||||||
chr1:35824539 | C | G | 1 | a0001c0002t0005g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.307-774C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824539 | |||||||
chr1:35824602 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.307-711C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824602 | |||||||
chr1:35824740 | A | G | 1 | a0001c0002t0008g0213 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.307-573A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824740 | |||||||
chr1:35824792 | C | T | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-521C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824792 | |||||||
chr1:35824809 | C | A | 8 | a0001c0001t0027g0070 a0001c0001t0034g0069 a0001c0003t0001g0150 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.307-504C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824809 | |||||||
chr1:35824908 | C | T | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-405C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824908 | |||||||
chr1:35824997 | A | G | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.307-316A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35824997 | |||||||
chr1:35825178 | G | T | 2 | a0001c0001t0004g0062 a0001c0005t0004g0068 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.307-135G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 3/17 | chr1 | 35825178 | |||||||
chr1:35825503 | C | T | 1 | a0001c0002t0014g0193 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.488+9C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 4/17 | chr1 | 35825503 | |||||||
chr1:35826149 | G | A | 11 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(8): Show |
13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.760+89G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 6/17 | chr1 | 35826149 | |||||||
chr1:35826290 | A | G | 2 | a0001c0002t0001g0204 a0001c0002t0017g0203 |
2 | NA18955.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.760+230A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 6/17 | chr1 | 35826290 | |||||||
chr1:35826489 | G | A | 1 | a0001c0002t0022g0217 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.761-259G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 6/17 | chr1 | 35826489 | |||||||
chr1:35826657 | A | G | 11 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(8): Show |
13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.761-91A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 6/17 | chr1 | 35826657 | |||||||
chr1:35827034 | T | C | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.848+199T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827034 | |||||||
chr1:35827063 | G | A | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+228G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827063 | |||||||
chr1:35827502 | A | G | 1 | a0001c0001t0002g0077 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.848+667A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827502 | |||||||
chr1:35827609 | T | C | 94 | a0001c0001t0001g0173 a0001c0001t0002g0239 a0001c0001t0002g0240 others(91): Show |
98 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.848+774T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827609 | |||||||
chr1:35827790 | CTT | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(223): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.848+974_848+975del others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35827790 | ||||||
chr1:35827790 | CTTT | C | 9 | a0001c0001t0002g0241 a0001c0001t0027g0070 a0001c0001t0034g0069 others(6): Show |
9 | HG01069.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.848+973_848+975del others(3): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35827790 | ||||||
chr1:35827790 | CTTTT | C | 11 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(8): Show |
13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.848+972_848+975del others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35827790 | ||||||
chr1:35827883 | T | C | 2 | a0001c0001t0004g0062 a0001c0005t0004g0068 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.848+1048T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35827883 | |||||||
chr1:35828012 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.848+1177T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828012 | |||||||
chr1:35828082 | A | G | 3 | a0001c0001t0015g0072 a0001c0001t0015g0073 a0001c0001t0025g0071 |
3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.848+1247A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828082 | |||||||
chr1:35828290 | G | A | 8 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(5): Show |
9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+1455G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828290 | |||||||
chr1:35828470 | A | G | 1 | a0001c0001t0002g0081 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.848+1635A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828470 | |||||||
chr1:35828474 | G | T | 7 | a0001c0002t0001g0170 a0001c0002t0001g0192 a0001c0002t0001g0218 others(4): Show |
7 | HG02486.hp2 HG03041.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.848+1639G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828474 | |||||||
chr1:35828539 | G | T | 1 | a0001c0001t0002g0092 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.848+1704G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828539 | |||||||
chr1:35828581 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.848+1746G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828581 | |||||||
chr1:35828712 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.848+1877G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828712 | |||||||
chr1:35828712 | G | C | 1 | a0001c0001t0002g0078 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.848+1877G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828712 | |||||||
chr1:35828881 | G | T | 1 | a0001c0001t0003g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848+2046G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35828881 | |||||||
chr1:35829029 | C | A | 10 | a0001c0001t0002g0116 a0001c0001t0007g0016 a0001c0001t0007g0017 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.848+2194C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829029 | |||||||
chr1:35829031 | C | A | 225 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(222): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.848+2196C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829031 | |||||||
chr1:35829031 | C | CA | 8 | a0001c0001t0001g0173 a0001c0001t0002g0135 a0001c0001t0003g0047 others(5): Show |
8 | HG00642.hp1 HG00741.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+2196_848+2197i others(3): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829031 | |||||||
chr1:35829036 | C | A | 2 | a0001c0002t0001g0171 a0001c0002t0001g0178 |
2 | HG00140.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.848+2201C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829036 | |||||||
chr1:35829086 | G | T | 2 | a0001c0001t0003g0032 a0001c0001t0003g0033 |
2 | NA18969.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.848+2251G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829086 | |||||||
chr1:35829309 | GA | G | 11 | a0001c0001t0001g0011 a0001c0001t0003g0020 a0001c0001t0004g0062 others(8): Show |
11 | HG01891.hp2 HG01943.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.849-2102delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829309 | ||||||
chr1:35829475 | A | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | NA18944.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.849-1952A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829475 | |||||||
chr1:35829552 | C | T | 2 | a0001c0001t0009g0056 a0001c0001t0009g0057 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.849-1875C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829552 | |||||||
chr1:35829809 | C | T | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-1618C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35829809 | |||||||
chr1:35829840 | T | TA | 81 | a0001c0001t0001g0173 a0001c0001t0002g0111 a0001c0001t0002g0117 others(78): Show |
85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.849-1561dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829840 | ||||||
chr1:35829840 | T | TAA | 10 | a0001c0002t0001g0009 a0001c0002t0001g0184 a0001c0002t0001g0186 others(7): Show |
10 | HG02040.hp1 HG02109.hp1 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-1562_849-1561d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829840 | ||||||
chr1:35829840 | TA | T | 7 | a0001c0001t0001g0067 a0001c0001t0003g0004 a0001c0001t0003g0031 others(4): Show |
9 | HG00280.hp2 HG00323.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.849-1561delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829840 | ||||||
chr1:35829840 | TAA | T | 13 | a0001c0001t0004g0054 a0001c0001t0004g0250 a0001c0001t0004g0252 others(10): Show |
13 | HG01169.hp1 HG01255.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.849-1562_849-1561d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35829840 | ||||||
chr1:35830143 | CA | C | 142 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(139): Show |
151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.849-1265delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35830143 | ||||||
chr1:35830143 | CAA | C | 100 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(97): Show |
104 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.849-1266_849-1265d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35830143 | ||||||
chr1:35830574 | T | A | 5 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(2): Show |
5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-853T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830574 | |||||||
chr1:35830691 | T | C | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.849-736T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830691 | |||||||
chr1:35830724 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849-703C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830724 | |||||||
chr1:35830827 | T | C | 13 | a0001c0001t0003g0004 a0001c0001t0003g0023 a0001c0001t0003g0038 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.849-600T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830827 | |||||||
chr1:35830840 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849-587C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830840 | |||||||
chr1:35830843 | G | A | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.849-584G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830843 | |||||||
chr1:35830850 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.849-577T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35830850 | |||||||
chr1:35830973 | C | CA | 15 | a0001c0001t0002g0083 a0001c0001t0002g0098 a0001c0001t0002g0135 others(12): Show |
15 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.849-435dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr1 | 35830973 | ||||||
chr1:35831099 | C | T | 1 | a0001c0002t0001g0214 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.849-328C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35831099 | |||||||
chr1:35831369 | A | T | 1 | a0001c0002t0001g0225 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.849-58A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 7/17 | chr1 | 35831369 | |||||||
chr1:35831998 | T | C | 1 | a0001c0001t0003g0047 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1117-59T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 9/17 | chr1 | 35831998 | |||||||
chr1:35832747 | G | C | 88 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(85): Show |
95 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1379+177G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35832747 | |||||||
chr1:35832824 | C | T | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+254C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35832824 | |||||||
chr1:35833150 | G | A | 3 | a0001c0001t0011g0007 a0001c0001t0012g0151 a0001c0001t0012g0253 |
4 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379+580G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833150 | |||||||
chr1:35833256 | C | T | 1 | a0001c0002t0001g0190 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1379+686C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833256 | |||||||
chr1:35833269 | C | T | 1 | a0001c0002t0001g0216 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1379+699C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833269 | |||||||
chr1:35833271 | G | C | 115 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(112): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1379+701G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833271 | |||||||
chr1:35833273 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(13): Show |
17 | HG01109.hp1 HG01934.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1379+703G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833273 | |||||||
chr1:35833371 | A | G | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1380-619A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833371 | |||||||
chr1:35833429 | C | T | 248 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(245): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1380-561C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 11/17 | chr1 | 35833429 | |||||||
chr1:35834316 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1564+142T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834316 | |||||||
chr1:35834366 | C | T | 4 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0026 others(1): Show |
4 | HG01175.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564+192C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834366 | |||||||
chr1:35834527 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1564+353C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834527 | |||||||
chr1:35834727 | GCT | G | 39 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0020 others(36): Show |
40 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1564+556_1564+557d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35834727 | ||||||
chr1:35834750 | C | T | 2 | a0001c0001t0016g0247 a0001c0001t0016g0249 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1564+576C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834750 | |||||||
chr1:35834812 | C | G | 1 | a0001c0002t0001g0010 | 2 | NA18970.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1564+638C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834812 | |||||||
chr1:35834820 | C | G | 7 | a0001c0001t0034g0069 a0001c0003t0001g0150 a0001c0003t0004g0152 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1564+646C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834820 | |||||||
chr1:35834974 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1564+800G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35834974 | |||||||
chr1:35835006 | C | CT | 24 | a0001c0001t0001g0147 a0001c0001t0002g0091 a0001c0001t0002g0110 others(21): Show |
25 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1565-806dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35835006 | ||||||
chr1:35835006 | C | CTT | 83 | a0001c0001t0001g0173 a0001c0001t0002g0239 a0001c0001t0002g0240 others(80): Show |
87 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1565-807_1565-806d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35835006 | ||||||
chr1:35835006 | C | CTTT | 9 | a0001c0002t0001g0176 a0001c0002t0001g0181 a0001c0002t0001g0209 others(6): Show |
9 | HG01071.hp1 HG01175.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565-808_1565-806d others(5): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35835006 | ||||||
chr1:35835006 | CT | C | 33 | a0001c0001t0003g0004 a0001c0001t0003g0023 a0001c0001t0003g0025 others(30): Show |
34 | HG00558.hp1 HG01255.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.1565-806delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr1 | 35835006 | ||||||
chr1:35835204 | G | A | 1 | a0001c0001t0031g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1565-630G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35835204 | |||||||
chr1:35835248 | G | C | 4 | a0001c0001t0009g0055 a0001c0001t0009g0056 a0001c0001t0009g0057 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565-586G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35835248 | |||||||
chr1:35835303 | C | G | 1 | a0001c0001t0004g0061 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1565-531C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35835303 | |||||||
chr1:35835621 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1565-213G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 12/17 | chr1 | 35835621 | |||||||
chr1:35836202 | G | A | 11 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(8): Show |
13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1724+209G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836202 | |||||||
chr1:35836571 | G | A | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1724+578G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836571 | |||||||
chr1:35836571 | G | T | 1 | a0001c0001t0002g0060 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1724+578G>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836571 | |||||||
chr1:35836602 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0141 |
2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1724+609G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836602 | |||||||
chr1:35836688 | C | T | 1 | a0001c0001t0015g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1724+695C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35836688 | |||||||
chr1:35837375 | C | T | 1 | a0001c0005t0004g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1724+1382C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35837375 | |||||||
chr1:35837446 | A | G | 1 | a0001c0002t0014g0189 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1724+1453A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35837446 | |||||||
chr1:35837620 | T | C | 1 | a0001c0002t0001g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1724+1627T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35837620 | |||||||
chr1:35838102 | C | T | 1 | a0001c0001t0031g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1724+2109C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838102 | |||||||
chr1:35838138 | C | T | 7 | a0001c0001t0034g0069 a0001c0003t0001g0150 a0001c0003t0004g0152 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1724+2145C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838138 | |||||||
chr1:35838174 | T | C | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1724+2181T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838174 | |||||||
chr1:35838294 | A | G | 2 | a0001c0002t0001g0206 a0001c0002t0001g0207 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1724+2301A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838294 | |||||||
chr1:35838631 | G | A | 1 | a0001c0002t0008g0185 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1725-2534G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35838631 | |||||||
chr1:35838920 | C | CT | 28 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0001g0144 others(25): Show |
29 | HG00280.hp2 HG00323.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1725-2235dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 35838920 | ||||||
chr1:35839301 | C | T | 2 | a0001c0002t0001g0218 a0001c0002t0001g0231 |
2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1725-1864C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35839301 | |||||||
chr1:35839417 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1725-1748C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35839417 | |||||||
chr1:35839518 | T | C | 1 | a0001c0002t0005g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1725-1647T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35839518 | |||||||
chr1:35839762 | T | C | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1725-1403T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35839762 | |||||||
chr1:35839966 | C | CA | 17 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(14): Show |
18 | HG01109.hp1 HG01934.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1725-1183dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 35839966 | ||||||
chr1:35839966 | CA | C | 6 | a0001c0001t0002g0080 a0001c0001t0016g0249 a0001c0001t0027g0070 others(3): Show |
6 | HG01168.hp1 HG01261.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725-1183delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 35839966 | ||||||
chr1:35840105 | C | T | 5 | a0001c0002t0001g0170 a0001c0002t0001g0192 a0001c0002t0004g0162 others(2): Show |
5 | NA18941.hp1 NA18972.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725-1060C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35840105 | |||||||
chr1:35840152 | C | T | 1 | a0001c0001t0004g0061 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1725-1013C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35840152 | |||||||
chr1:35840166 | T | G | 20 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(17): Show |
20 | HG01074.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1725-999T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35840166 | |||||||
chr1:35840595 | G | C | 1 | a0001c0001t0002g0127 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1725-570G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35840595 | |||||||
chr1:35841149 | C | T | 1 | a0001c0005t0004g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1725-16C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 13/17 | chr1 | 35841149 | |||||||
chr1:35841519 | G | A | 5 | a0001c0002t0001g0187 a0001c0002t0001g0190 a0001c0002t0001g0199 others(2): Show |
5 | HG02258.hp2 HG02273.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.2040+39G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 14/17 | chr1 | 35841519 | |||||||
chr1:35841532 | A | T | 1 | a0001c0001t0002g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2040+52A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 14/17 | chr1 | 35841532 | |||||||
chr1:35841572 | T | C | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2041-44T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 14/17 | chr1 | 35841572 | |||||||
chr1:35841811 | C | CATAT | 10 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2175+85_2175+88dup others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841811 | C | CATATATA others(5): Show |
1 | a0001c0001t0012g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2175+77_2175+88dup others(12): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841811 | C | CATATATA others(9): Show |
2 | a0001c0001t0016g0247 a0001c0001t0016g0249 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2175+73_2175+88dup others(16): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841811 | C | CATATATA others(11): Show |
4 | a0001c0001t0004g0250 a0001c0001t0011g0007 a0001c0001t0012g0253 others(1): Show |
5 | HG01255.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2175+71_2175+88dup others(18): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841811 | C | CATATATA others(17): Show |
1 | a0001c0001t0004g0251 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2175+80_2175+81ins others(24): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841811 | C | CATATATA others(19): Show |
1 | a0001c0001t0004g0013 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.2175+80_2175+81ins others(26): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841811 | C | CATATATA others(13): Show |
2 | a0001c0001t0004g0054 a0001c0001t0004g0252 |
2 | HG03491.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2175+69_2175+88dup others(20): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841811 | CAT | C | 113 | a0001c0001t0001g0011 a0001c0001t0001g0139 a0001c0001t0001g0145 others(110): Show |
117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2175+87_2175+88del others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841811 | CATAT | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(86): Show |
96 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2175+85_2175+88del others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841811 | CATATATA others(5): Show |
C | 3 | a0001c0001t0015g0072 a0001c0001t0015g0073 a0001c0001t0025g0071 |
3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2175+77_2175+88del others(12): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35841811 | ||||||
chr1:35841839 | C | T | 8 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(5): Show |
9 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.2175+89C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35841839 | |||||||
chr1:35841848 | T | A | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2175+98T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35841848 | |||||||
chr1:35842160 | C | T | 1 | a0001c0001t0025g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2175+410C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842160 | |||||||
chr1:35842166 | C | G | 2 | a0001c0002t0001g0214 a0001c0002t0001g0235 |
2 | HG01123.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2175+416C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842166 | |||||||
chr1:35842296 | A | G | 88 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(85): Show |
95 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2175+546A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842296 | |||||||
chr1:35842350 | T | G | 2 | a0001c0001t0008g0140 a0001c0001t0023g0143 |
2 | HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2175+600T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842350 | |||||||
chr1:35842577 | C | T | 1 | a0001c0003t0004g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2175+827C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842577 | |||||||
chr1:35842663 | G | A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG01884.hp2 HG02717.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2175+913G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842663 | |||||||
chr1:35842750 | C | T | 94 | a0001c0001t0001g0173 a0001c0001t0002g0239 a0001c0001t0002g0240 others(91): Show |
98 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2175+1000C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842750 | |||||||
chr1:35842762 | A | G | 3 | a0001c0001t0015g0072 a0001c0001t0015g0073 a0001c0001t0025g0071 |
3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2175+1012A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842762 | |||||||
chr1:35842863 | T | A | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2175+1113T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35842863 | |||||||
chr1:35843249 | T | G | 1 | a0001c0001t0031g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2175+1499T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35843249 | |||||||
chr1:35843397 | G | A | 4 | a0001c0001t0009g0055 a0001c0001t0009g0056 a0001c0001t0009g0057 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2175+1647G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35843397 | |||||||
chr1:35843659 | GA | G | 7 | a0001c0001t0002g0090 a0001c0003t0001g0150 a0001c0003t0004g0152 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2175+1919delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35843659 | ||||||
chr1:35844336 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2175+2586A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844336 | |||||||
chr1:35844436 | T | C | 4 | a0001c0001t0009g0055 a0001c0001t0009g0056 a0001c0001t0009g0057 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2175+2686T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844436 | |||||||
chr1:35844533 | C | G | 3 | a0001c0001t0015g0072 a0001c0001t0015g0073 a0001c0001t0025g0071 |
3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2175+2783C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844533 | |||||||
chr1:35844662 | C | T | 1 | a0001c0001t0004g0251 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2175+2912C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844662 | |||||||
chr1:35844720 | G | C | 1 | a0001c0001t0002g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2175+2970G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844720 | |||||||
chr1:35844901 | A | C | 1 | a0001c0002t0001g0215 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2175+3151A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35844901 | |||||||
chr1:35845102 | TTGTAATC others(35): Show |
T | 17 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0251 others(14): Show |
19 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.2175+3381_2175+342 others(46): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845102 | ||||||
chr1:35845113 | CT | C | 218 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(215): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2175+3381delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845113 | ||||||
chr1:35845113 | CTT | C | 11 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0002 others(8): Show |
12 | HG01934.hp1 HG01943.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.2175+3380_2175+338 others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845113 | ||||||
chr1:35845113 | CTTTTTTT others(36): Show |
C | 2 | a0001c0001t0004g0250 a0001c0003t0004g0156 |
2 | HG02922.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2175+3380_2175+342 others(47): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845113 | ||||||
chr1:35845114 | T | C | 1 | a0001c0001t0002g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2175+3364T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845114 | |||||||
chr1:35845114 | T | G | 1 | a0001c0001t0004g0061 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2175+3364T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845114 | |||||||
chr1:35845131 | T | G | 1 | a0001c0001t0002g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2175+3381T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845131 | |||||||
chr1:35845155 | C | CT | 16 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0066 others(13): Show |
16 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.2175+3422dupT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845155 | ||||||
chr1:35845155 | CT | C | 6 | a0001c0001t0002g0104 a0001c0001t0003g0038 a0001c0001t0025g0071 others(3): Show |
6 | HG03491.hp1 HG06807.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.2175+3422delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845155 | ||||||
chr1:35845196 | CT | C | 55 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0020 others(52): Show |
58 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2175+3462delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845196 | ||||||
chr1:35845196 | CTT | C | 98 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(95): Show |
105 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.2175+3461_2175+346 others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35845196 | ||||||
chr1:35845212 | TG | T | 92 | a0001c0001t0001g0173 a0001c0001t0002g0239 a0001c0001t0002g0240 others(89): Show |
96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2175+3463delG | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845212 | |||||||
chr1:35845294 | G | A | 1 | a0001c0001t0009g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2175+3544G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845294 | |||||||
chr1:35845386 | T | C | 2 | a0001c0001t0004g0013 a0001c0001t0004g0251 |
3 | HG00280.hp2 HG00323.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2175+3636T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845386 | |||||||
chr1:35845426 | C | T | 1 | a0001c0001t0006g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2175+3676C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845426 | |||||||
chr1:35845459 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2175+3709G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845459 | |||||||
chr1:35845466 | C | G | 39 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0020 others(36): Show |
40 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.2175+3716C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845466 | |||||||
chr1:35845472 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2175+3722G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845472 | |||||||
chr1:35845542 | T | G | 11 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(8): Show |
13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2175+3792T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845542 | |||||||
chr1:35845591 | T | C | 1 | a0001c0001t0010g0105 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2175+3841T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845591 | |||||||
chr1:35845748 | A | C | 1 | a0001c0002t0005g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2175+3998A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35845748 | |||||||
chr1:35846051 | G | A | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-4106G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846051 | |||||||
chr1:35846117 | T | C | 5 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(2): Show |
5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-4040T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846117 | |||||||
chr1:35846381 | A | G | 2 | a0001c0001t0003g0032 a0001c0001t0003g0033 |
2 | NA18969.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2176-3776A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846381 | |||||||
chr1:35846401 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2176-3756T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846401 | |||||||
chr1:35846604 | GAT | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(31): Show |
36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.2176-3528_2176-352 others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35846604 | ||||||
chr1:35846604 | GATAT | G | 197 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(194): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.2176-3530_2176-352 others(8): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35846604 | ||||||
chr1:35846675 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2176-3482C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846675 | |||||||
chr1:35846724 | A | G | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-3433A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846724 | |||||||
chr1:35846864 | A | G | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2176-3293A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846864 | |||||||
chr1:35846865 | C | T | 1 | a0001c0002t0005g0159 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2176-3292C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35846865 | |||||||
chr1:35847012 | A | G | 5 | a0001c0002t0001g0170 a0001c0002t0001g0192 a0001c0002t0004g0162 others(2): Show |
5 | NA18941.hp1 NA18972.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2176-3145A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847012 | |||||||
chr1:35847057 | A | ACATCCTC others(137): Show |
1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2176-3082_2176-308 others(148): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35847057 | ||||||
chr1:35847059 | A | G | 1 | a0001c0002t0005g0159 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2176-3098A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847059 | |||||||
chr1:35847254 | G | C | 1 | a0001c0002t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2176-2903G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847254 | |||||||
chr1:35847285 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2176-2872G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847285 | |||||||
chr1:35847440 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2176-2717G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847440 | |||||||
chr1:35847685 | TAA | T | 127 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(124): Show |
135 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.2176-2471_2176-247 others(6): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847685 | |||||||
chr1:35847742 | A | G | 1 | a0001c0002t0001g0188 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2176-2415A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35847742 | |||||||
chr1:35847968 | T | TAAAGAAT others(324): Show |
1 | a0001c0001t0012g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2176-2173_2176-217 others(335): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35847968 | ||||||
chr1:35847968 | T | TAAAGAAT others(326): Show |
1 | a0001c0001t0012g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2176-2173_2176-217 others(337): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35847968 | ||||||
chr1:35847968 | T | TAAAGAAT others(328): Show |
1 | a0001c0001t0011g0007 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2176-2173_2176-217 others(339): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35847968 | ||||||
chr1:35848064 | G | A | 11 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(8): Show |
13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2176-2093G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848064 | |||||||
chr1:35848127 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(12): Show |
16 | HG01109.hp1 HG01934.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2176-2030T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848127 | |||||||
chr1:35848273 | C | G | 1 | a0001c0002t0001g0231 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2176-1884C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848273 | |||||||
chr1:35848402 | A | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0138 others(82): Show |
92 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.2176-1755A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848402 | |||||||
chr1:35848451 | CT | C | 90 | a0001c0001t0001g0173 a0001c0001t0002g0239 a0001c0001t0002g0240 others(87): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2176-1702delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35848451 | ||||||
chr1:35848598 | G | A | 90 | a0001c0001t0001g0173 a0001c0001t0002g0239 a0001c0001t0002g0240 others(87): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2176-1559G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848598 | |||||||
chr1:35848637 | GT | G | 8 | a0001c0001t0002g0107 a0001c0001t0002g0241 a0001c0001t0003g0024 others(5): Show |
8 | HG01069.hp2 HG01175.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2176-1506delT | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35848637 | ||||||
chr1:35848852 | A | G | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176-1305A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848852 | |||||||
chr1:35848865 | A | G | 56 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0060 others(53): Show |
60 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.2176-1292A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35848865 | |||||||
chr1:35849026 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2176-1131A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849026 | |||||||
chr1:35849087 | G | A | 11 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(8): Show |
13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2176-1070G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849087 | |||||||
chr1:35849114 | T | G | 1 | a0001c0002t0001g0226 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2176-1043T>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849114 | |||||||
chr1:35849128 | A | G | 1 | a0001c0003t0004g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2176-1029A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849128 | |||||||
chr1:35849260 | A | G | 90 | a0001c0001t0001g0173 a0001c0001t0002g0239 a0001c0001t0002g0240 others(87): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2176-897A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849260 | |||||||
chr1:35849518 | C | CA | 25 | a0001c0001t0002g0125 a0001c0001t0003g0024 a0001c0001t0003g0032 others(22): Show |
26 | HG00280.hp2 HG00323.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.2176-619dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849518 | ||||||
chr1:35849518 | C | CAA | 6 | a0001c0001t0004g0061 a0001c0001t0011g0007 a0001c0001t0012g0151 others(3): Show |
7 | HG02129.hp2 HG02970.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2176-620_2176-619d others(4): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849518 | ||||||
chr1:35849518 | CA | C | 10 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0002g0089 others(7): Show |
11 | HG01069.hp2 HG01884.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2176-619delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849518 | ||||||
chr1:35849686 | C | CA | 10 | a0001c0001t0001g0063 a0001c0001t0004g0013 a0001c0001t0004g0054 others(7): Show |
11 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.2176-452dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849686 | ||||||
chr1:35849686 | CA | C | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0006 others(64): Show |
73 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2176-452delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 35849686 | ||||||
chr1:35849793 | G | C | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2176-364G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849793 | |||||||
chr1:35849823 | C | T | 1 | a0001c0002t0001g0231 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2176-334C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849823 | |||||||
chr1:35849850 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2176-307C>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35849850 | |||||||
chr1:35850032 | G | C | 4 | a0001c0001t0009g0055 a0001c0001t0009g0056 a0001c0001t0009g0057 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176-125G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 15/17 | chr1 | 35850032 | |||||||
chr1:35850330 | C | A | 8 | a0001c0001t0027g0070 a0001c0001t0034g0069 a0001c0003t0001g0150 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.2277+72C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850330 | |||||||
chr1:35850703 | G | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(245): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2278-151G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850703 | |||||||
chr1:35850736 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2278-118G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850736 | |||||||
chr1:35850780 | C | CA | 86 | a0001c0001t0001g0011 a0001c0001t0001g0173 a0001c0001t0002g0001 others(83): Show |
94 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.2278-55dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 35850780 | ||||||
chr1:35850780 | C | CAA | 19 | a0001c0001t0002g0081 a0001c0001t0002g0090 a0001c0001t0002g0096 others(16): Show |
19 | HG00673.hp1 HG02056.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.2278-56_2278-55dup others(2): Show |
AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 35850780 | ||||||
chr1:35850780 | CA | C | 6 | a0001c0002t0001g0197 a0001c0003t0001g0150 a0001c0003t0004g0152 others(3): Show |
6 | HG02055.hp2 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2278-55delA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 35850780 | ||||||
chr1:35850794 | A | C | 1 | a0001c0002t0004g0162 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2278-60A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850794 | |||||||
chr1:35850795 | A | C | 5 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(2): Show |
5 | HG01069.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2278-59A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850795 | |||||||
chr1:35850800 | C | A | 48 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(45): Show |
49 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(46): Show |
intron_variant | MODIFIER | c.2278-54C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850800 | |||||||
chr1:35850801 | A | C | 1 | a0001c0001t0002g0137 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2278-53A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | chr1 | 35850801 | |||||||
chr1:35850817 | C | CA | 246 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(243): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2278-27dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 35850817 | ||||||
chr1:35851077 | G | C | 32 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0023 others(29): Show |
33 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.2477+24G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851077 | |||||||
chr1:35851103 | A | T | 1 | a0001c0001t0002g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2477+50A>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851103 | |||||||
chr1:35851126 | A | G | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2477+73A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851126 | |||||||
chr1:35851410 | G | C | 1 | a0001c0001t0011g0007 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2477+357G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851410 | |||||||
chr1:35851440 | G | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(93): Show |
103 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.2477+387G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851440 | |||||||
chr1:35851779 | C | T | 10 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(7): Show |
12 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.2477+726C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851779 | |||||||
chr1:35851854 | T | A | 248 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(245): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2477+801T>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851854 | |||||||
chr1:35851870 | G | C | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(15): Show |
20 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2477+817G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851870 | |||||||
chr1:35851888 | G | A | 1 | a0001c0001t0033g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2477+835G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35851888 | |||||||
chr1:35852234 | C | T | 38 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0020 others(35): Show |
39 | HG00438.hp1 HG00558.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.2477+1181C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852234 | |||||||
chr1:35852290 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2478-1207G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852290 | |||||||
chr1:35852309 | G | C | 2 | a0001c0001t0004g0062 a0001c0005t0004g0068 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2478-1188G>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852309 | |||||||
chr1:35852564 | G | A | 248 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(245): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2478-933G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852564 | |||||||
chr1:35852858 | A | G | 1 | a0001c0005t0004g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2478-639A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852858 | |||||||
chr1:35852862 | A | C | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2478-635A>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852862 | |||||||
chr1:35852950 | T | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(245): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2478-547T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852950 | |||||||
chr1:35852976 | C | T | 2 | a0001c0002t0001g0206 a0001c0002t0001g0207 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2478-521C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35852976 | |||||||
chr1:35853033 | G | A | 1 | a0001c0001t0005g0244 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2478-464G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853033 | |||||||
chr1:35853047 | G | A | 1 | a0001c0001t0034g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2478-450G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853047 | |||||||
chr1:35853066 | T | C | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2478-431T>C | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853066 | |||||||
chr1:35853067 | G | A | 1 | a0001c0001t0027g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2478-430G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853067 | |||||||
chr1:35853110 | G | A | 6 | a0001c0003t0001g0150 a0001c0003t0004g0152 a0001c0003t0004g0154 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2478-387G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853110 | |||||||
chr1:35853119 | C | A | 247 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0064 others(244): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.2478-378C>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853119 | |||||||
chr1:35853120 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2478-377G>A | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853120 | |||||||
chr1:35853207 | C | T | 3 | a0001c0001t0015g0072 a0001c0001t0015g0073 a0001c0001t0025g0071 |
3 | HG02145.hp2 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2478-290C>T | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853207 | |||||||
chr1:35853248 | C | CA | 41 | a0001c0001t0002g0082 a0001c0001t0002g0127 a0001c0001t0002g0133 others(38): Show |
42 | HG00438.hp1 HG00558.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.2478-229dupA | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 35853248 | ||||||
chr1:35853265 | A | G | 11 | a0001c0001t0004g0013 a0001c0001t0004g0054 a0001c0001t0004g0250 others(8): Show |
13 | HG00280.hp2 HG00323.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.2478-232A>G | AGO4 | ENSG00000134698.11 | transcript | ENST00000373210.4 | protein_coding | 17/17 | chr1 | 35853265 |