Item | Value |
---|---|
geneid | 8726 |
ensemblid | ENSG00000074266.23 |
hgncid | 3188 |
symbol | EED |
name | embryonic ectoderm development |
refseq_nuc | NM_003797.5 |
refseq_prot | NP_003788.2 |
ensembl_nuc | ENST00000263360.11 |
ensembl_prot | ENSP00000263360.6 |
mane_status | MANE Select |
chr | chr11 |
start | 86244753 |
end | 86278810 |
strand | + |
ver | v1.2 |
region | chr11:86244753-86278810 |
region5000 | chr11:86239753-86283810 |
regionname0 | EED_chr11_86244753_86278810 |
regionname5000 | EED_chr11_86239753_86283810 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 441 | 391 | 84 | 60 | 189 | 14 | 42 | 149 | EED_chr11_86239753_86283810 | EED | MSERE others(436): Show |
chr11 | 86239753 | 86283810 |
a0002 | 0/0 | 441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | MSERE others(436): Show |
chr11 | 86239753 | 86283810 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1323 | 274 | 72 | 41 | 126 | 8 | 26 | EED_chr11_86239753_86283810 | EED | ATGTC others(1318): Show |
chr11 | 86239753 | 86283810 | ||
a0001c0002 | 0/1 | 1323 | 116 | 12 | 19 | 62 | 6 | 16 | EED_chr11_86239753_86283810 | EED | ATGTC others(1318): Show |
chr11 | 86239753 | 86283810 | ||
a0001c0003 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | ATGTC others(1318): Show |
chr11 | 86239753 | 86283810 | ||
a0002c0004 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | ATGTC others(1318): Show |
chr11 | 86239753 | 86283810 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2088 | 267 | 69 | 40 | 124 | 8 | 25 | EED_chr11_86239753_86283810 | EED | ATTCC others(2083): Show |
chr11 | 86239753 | 86283810 |
a0001c0001t0002 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | ATTCC others(2083): Show |
chr11 | 86239753 | 86283810 |
a0001c0001t0003 | 0/0 | 2088 | 2 | 0 | 1 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | ATTCC others(2083): Show |
chr11 | 86239753 | 86283810 |
a0001c0001t0004 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | ATTCC others(2083): Show |
chr11 | 86239753 | 86283810 |
a0001c0001t0005 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | ATTCC others(2083): Show |
chr11 | 86239753 | 86283810 |
a0001c0001t0006 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | ATTCC others(2083): Show |
chr11 | 86239753 | 86283810 |
a0001c0002t0001 | 0/1 | 2088 | 116 | 12 | 19 | 62 | 6 | 16 | EED_chr11_86239753_86283810 | EED | ATTCC others(2083): Show |
chr11 | 86239753 | 86283810 |
a0001c0003t0001 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | ATTCC others(2083): Show |
chr11 | 86239753 | 86283810 |
a0002c0004t0001 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | ATTCC others(2083): Show |
chr11 | 86239753 | 86283810 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 1 | 5 | 1 | 4 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0019 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0002 | 0/0 | 9 | 0 | 5 | 1 | 1 | 2 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0005 | 0/0 | 5 | 2 | 0 | 1 | 0 | 2 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0002c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0271 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0277 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0270 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0045 | EUR | IBS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0045 | EUR | IBS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0246 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0241 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | CDX | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0289 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0242 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0175 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0263 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0262 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0248 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0240 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0261 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | CHB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | LWK | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19054 | hp2 | a0002 | c0004 | t0001 | g0014 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | ASW | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ASW | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0265 | EUR | TSI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0268 | EUR | TSI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0169 | EUR | TSI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | GIH | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | USA | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0275 | REF | REF | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0067 | REF | REF | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:86245285 | A | G | 1 | a0002 | 1 | NA19054.hp2 | missense_variant | MODERATE | c.56A>G | p.Lys19Arg | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 533/2088 | 56/1326 | 19/441 | chr11 | 86245285 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:86257581 | C | T | 1 | a0001c0002 | 115 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
synonymous_variant | LOW | c.619C>T | p.Leu207Leu | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/12 | 1096/2088 | 619/1326 | 207/441 | chr11 | 86257581 | |||
chr11:86277015 | C | A | 1 | a0001c0003 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.1002C>A | p.Gly334Gly | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 10/12 | 1479/2088 | 1002/1326 | 334/441 | chr11 | 86277015 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:86244810 | G | C | 1 | a0001c0001t0004 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-420G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 420 | chr11 | 86244810 | ||||||
chr11:86244987 | G | A | 1 | a0001c0001t0005 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-243G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 243 | chr11 | 86244987 | ||||||
chr11:86245106 | G | T | 1 | a0001c0001t0003 | 2 | HG01934.hp1 NA18957.hp1 |
5_prime_UTR_variant | MODIFIER | c.-124G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 124 | chr11 | 86245106 | ||||||
chr11:86245204 | A | C | 1 | a0001c0001t0006 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 26 | chr11 | 86245204 | ||||||
chr11:86245208 | A | T | 1 | a0001c0001t0002 | 2 | HG02886.hp1 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-22A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 22 | chr11 | 86245208 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:86245361 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0296 |
5 | HG00408.hp1 HG00609.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+18C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245361 | |||||||
chr11:86245434 | G | T | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.114+91G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245434 | |||||||
chr11:86245436 | G | T | 13 | a0001c0001t0001g0048 a0001c0001t0001g0282 a0001c0001t0001g0283 others(10): Show |
14 | HG00323.hp1 HG00639.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+93G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245436 | |||||||
chr11:86245448 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.114+105G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245448 | |||||||
chr11:86245579 | C | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | NA18948.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.114+236C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245579 | |||||||
chr11:86246007 | G | T | 1 | a0001c0001t0001g0279 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.114+664G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246007 | |||||||
chr11:86246243 | T | TAACC | 2 | a0001c0001t0001g0022 a0001c0001t0001g0050 |
3 | HG03195.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.114+902_114+905dup others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 86246243 | ||||||
chr11:86246272 | C | G | 43 | a0001c0002t0001g0002 a0001c0002t0001g0021 a0001c0002t0001g0045 others(40): Show |
56 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.114+929C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246272 | |||||||
chr11:86246274 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0041 others(53): Show |
72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.114+931A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246274 | |||||||
chr11:86246416 | A | G | 39 | a0001c0001t0001g0206 a0001c0002t0001g0002 a0001c0002t0001g0021 others(36): Show |
52 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.114+1073A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246416 | |||||||
chr11:86246649 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0041 others(53): Show |
72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.114+1306A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246649 | |||||||
chr11:86246703 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(201): Show |
258 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.114+1360A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246703 | |||||||
chr11:86246725 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.114+1382C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246725 | |||||||
chr11:86246951 | C | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
12 | HG00140.hp2 HG00280.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.114+1608C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246951 | |||||||
chr11:86246957 | G | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+1614G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246957 | |||||||
chr11:86246988 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114+1645A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246988 | |||||||
chr11:86247107 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.114+1764A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247107 | |||||||
chr11:86247121 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.114+1778A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247121 | |||||||
chr11:86247345 | A | T | 119 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(116): Show |
151 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.114+2002A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247345 | |||||||
chr11:86247421 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.114+2078G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247421 | |||||||
chr11:86247428 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.114+2085A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247428 | |||||||
chr11:86247500 | G | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+2157G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247500 | |||||||
chr11:86247605 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.114+2262G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247605 | |||||||
chr11:86247718 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(103): Show |
131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.114+2375T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247718 | |||||||
chr11:86248001 | A | G | 49 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0020 others(46): Show |
62 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.115-2295A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248001 | |||||||
chr11:86248119 | T | G | 3 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0001c0002t0001g0247 |
3 | HG01106.hp1 HG01978.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.115-2177T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248119 | |||||||
chr11:86248200 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0050 |
3 | HG03195.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.115-2096A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248200 | |||||||
chr11:86248284 | A | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0108 others(12): Show |
19 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.115-2012A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248284 | |||||||
chr11:86248309 | G | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.115-1987G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248309 | |||||||
chr11:86248322 | G | C | 119 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(116): Show |
151 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.115-1974G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248322 | |||||||
chr11:86248429 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(196): Show |
250 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.115-1867C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248429 | |||||||
chr11:86248628 | G | C | 119 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(116): Show |
151 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.115-1668G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248628 | |||||||
chr11:86248741 | G | GGGCGCA | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.115-1553_115-1548d others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 86248741 | ||||||
chr11:86248766 | C | A | 1 | a0001c0001t0001g0052 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.115-1530C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248766 | |||||||
chr11:86248789 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(76): Show |
98 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-1507T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248789 | |||||||
chr11:86249162 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0041 others(53): Show |
72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.115-1134A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249162 | |||||||
chr11:86249298 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.115-998A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249298 | |||||||
chr11:86249347 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.115-949A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249347 | |||||||
chr11:86249381 | G | GA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(99): Show |
127 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.115-898dupA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 86249381 | ||||||
chr11:86249381 | G | GAA | 6 | a0001c0001t0001g0053 a0001c0001t0001g0121 a0001c0001t0001g0122 others(3): Show |
6 | HG01069.hp2 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-899_115-898dup others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 86249381 | ||||||
chr11:86249615 | G | T | 1 | a0001c0002t0001g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.115-681G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249615 | |||||||
chr11:86249680 | CAAT | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(76): Show |
98 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-615_115-613del others(3): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249680 | |||||||
chr11:86249750 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.115-546G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249750 | |||||||
chr11:86249847 | C | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
10 | HG02572.hp1 HG02809.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-449C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249847 | |||||||
chr11:86250124 | C | T | 92 | a0001c0001t0001g0164 a0001c0001t0001g0202 a0001c0001t0001g0203 others(89): Show |
118 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.115-172C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86250124 | |||||||
chr11:86250563 | A | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG02976.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+115A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250563 | |||||||
chr11:86250578 | GT | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(75): Show |
97 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.267+141delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 86250578 | ||||||
chr11:86250604 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(76): Show |
98 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.267+156G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250604 | |||||||
chr11:86250702 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.267+254T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250702 | |||||||
chr11:86250721 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.267+273A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250721 | |||||||
chr11:86250728 | G | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG02976.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+280G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250728 | |||||||
chr11:86250831 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.267+383G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250831 | |||||||
chr11:86250955 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+507G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250955 | |||||||
chr11:86251252 | T | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+804T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251252 | |||||||
chr11:86251311 | G | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0041 others(53): Show |
72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.268-837G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251311 | |||||||
chr11:86251339 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.268-809C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251339 | |||||||
chr11:86251516 | T | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(221): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.268-632T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251516 | |||||||
chr11:86251905 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(20): Show |
37 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.268-243G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251905 | |||||||
chr11:86251959 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.268-189C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251959 | |||||||
chr11:86252105 | G | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.268-43G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86252105 | |||||||
chr11:86252510 | C | CA | 6 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(3): Show |
13 | HG00140.hp2 HG00280.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+270_360+271ins others(1): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252510 | |||||||
chr11:86252511 | G | GC | 45 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(42): Show |
53 | HG00408.hp2 HG01074.hp2 HG01496.hp1 others(50): Show |
intron_variant | MODIFIER | c.360+271_360+272ins others(1): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252511 | |||||||
chr11:86252511 | G | GT | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(178): Show |
239 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.360+272dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86252511 | ||||||
chr11:86252511 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(3): Show |
13 | HG00140.hp2 HG00280.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+271G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252511 | |||||||
chr11:86252512 | T | TTC | 60 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0022 others(57): Show |
80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.360+272_360+273ins others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252512 | |||||||
chr11:86252513 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0106 others(2): Show |
5 | HG01070.hp1 HG01168.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+273C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252513 | |||||||
chr11:86252514 | C | CT | 42 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0033 others(39): Show |
49 | HG00408.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.360+289dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86252514 | ||||||
chr11:86252514 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0022 others(57): Show |
80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.360+274C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252514 | |||||||
chr11:86252515 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0106 others(1): Show |
4 | HG01070.hp1 HG01168.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+275T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252515 | |||||||
chr11:86252577 | C | T | 93 | a0001c0001t0001g0164 a0001c0001t0001g0202 a0001c0001t0001g0203 others(90): Show |
119 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.360+337C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252577 | |||||||
chr11:86252590 | T | C | 93 | a0001c0001t0001g0164 a0001c0001t0001g0202 a0001c0001t0001g0203 others(90): Show |
119 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.360+350T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252590 | |||||||
chr11:86252744 | A | ATTGTTG | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.360+522_360+527dup others(6): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86252744 | ||||||
chr11:86252899 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.360+659A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252899 | |||||||
chr11:86253045 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.360+805G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253045 | |||||||
chr11:86253386 | T | A | 1 | a0001c0001t0001g0144 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.360+1146T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253386 | |||||||
chr11:86253470 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0118 |
2 | NA18991.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.360+1230A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253470 | |||||||
chr11:86253585 | C | T | 137 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(134): Show |
171 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.360+1345C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253585 | |||||||
chr11:86253643 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0032 others(58): Show |
78 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.360+1403T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253643 | |||||||
chr11:86253687 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.360+1447T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253687 | |||||||
chr11:86253768 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0160 |
3 | NA18953.hp1 NA18974.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.361-1454C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253768 | |||||||
chr11:86253845 | C | T | 92 | a0001c0001t0001g0164 a0001c0001t0001g0202 a0001c0001t0001g0203 others(89): Show |
118 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.361-1377C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253845 | |||||||
chr11:86253864 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.361-1358G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253864 | |||||||
chr11:86253903 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0032 others(58): Show |
78 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.361-1319C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253903 | |||||||
chr11:86253934 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0032 others(58): Show |
78 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.361-1288G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253934 | |||||||
chr11:86253940 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.361-1282C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253940 | |||||||
chr11:86254040 | C | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-1182C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254040 | |||||||
chr11:86254048 | C | CA | 25 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(22): Show |
25 | HG00738.hp1 HG01099.hp1 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.361-1147dupA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | ||||||
chr11:86254048 | C | CAA | 7 | a0001c0001t0001g0070 a0001c0001t0001g0164 a0001c0001t0001g0202 others(4): Show |
8 | HG01168.hp2 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-1148_361-1147d others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | ||||||
chr11:86254048 | C | CAAA | 16 | a0001c0002t0001g0002 a0001c0002t0001g0045 a0001c0002t0001g0046 others(13): Show |
26 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.361-1149_361-1147d others(5): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | ||||||
chr11:86254048 | C | CAAAA | 18 | a0001c0002t0001g0021 a0001c0002t0001g0197 a0001c0002t0001g0198 others(15): Show |
20 | HG00738.hp2 HG01123.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.361-1150_361-1147d others(6): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | ||||||
chr11:86254048 | C | CAAAAA | 31 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0020 others(28): Show |
41 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.361-1151_361-1147d others(7): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | ||||||
chr11:86254048 | C | CAAAAAA | 19 | a0001c0002t0001g0037 a0001c0002t0001g0038 a0001c0002t0001g0039 others(16): Show |
22 | HG01106.hp1 HG01978.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.361-1152_361-1147d others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | ||||||
chr11:86254048 | CA | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0030 others(60): Show |
79 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.361-1147delA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | ||||||
chr11:86254048 | CAAA | C | 21 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(18): Show |
27 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.361-1149_361-1147d others(5): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | ||||||
chr11:86254048 | CAAAAAAA others(9): Show |
C | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
25 | HG00741.hp1 HG01192.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.361-1162_361-1147d others(18): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | ||||||
chr11:86254063 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.361-1159A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254063 | |||||||
chr11:86254069 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-1153A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254069 | |||||||
chr11:86254105 | G | A | 1 | a0001c0002t0001g0179 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.361-1117G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254105 | |||||||
chr11:86254237 | T | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-985T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254237 | |||||||
chr11:86254323 | G | GT | 33 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0052 others(30): Show |
35 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.361-884dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254323 | ||||||
chr11:86254372 | G | A | 1 | a0001c0002t0001g0265 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.361-850G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254372 | |||||||
chr11:86254385 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-837A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254385 | |||||||
chr11:86254403 | T | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-819T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254403 | |||||||
chr11:86254541 | G | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0137 a0001c0001t0001g0138 |
4 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-681G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254541 | |||||||
chr11:86254566 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.361-656G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254566 | |||||||
chr11:86254622 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.361-600T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254622 | |||||||
chr11:86254672 | G | C | 1 | a0001c0002t0001g0266 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.361-550G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254672 | |||||||
chr11:86254708 | C | T | 2 | a0001c0002t0001g0177 a0001c0002t0001g0195 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.361-514C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254708 | |||||||
chr11:86254715 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.361-507C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254715 | |||||||
chr11:86254764 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0089 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.361-458G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254764 | |||||||
chr11:86254766 | GC | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
25 | HG00741.hp1 HG01192.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.361-455delC | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254766 | |||||||
chr11:86254780 | G | A | 1 | a0001c0002t0001g0180 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.361-442G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254780 | |||||||
chr11:86254867 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(197): Show |
251 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.361-355T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254867 | |||||||
chr11:86254882 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.361-340A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254882 | |||||||
chr11:86254896 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0010 others(85): Show |
114 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.361-326C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254896 | |||||||
chr11:86254911 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.361-311G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254911 | |||||||
chr11:86255009 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.361-213G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86255009 | |||||||
chr11:86255135 | G | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(196): Show |
250 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.361-87G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86255135 | |||||||
chr11:86255500 | A | C | 92 | a0001c0001t0001g0164 a0001c0001t0001g0202 a0001c0001t0001g0203 others(89): Show |
118 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.426+213A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255500 | |||||||
chr11:86255517 | G | A | 1 | a0001c0002t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.426+230G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255517 | |||||||
chr11:86255518 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0032 others(58): Show |
78 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.426+231A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255518 | |||||||
chr11:86255533 | G | A | 92 | a0001c0001t0001g0164 a0001c0001t0001g0202 a0001c0001t0001g0203 others(89): Show |
118 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.426+246G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255533 | |||||||
chr11:86255544 | T | C | 88 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0010 others(85): Show |
114 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.426+257T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255544 | |||||||
chr11:86255623 | C | G | 92 | a0001c0001t0001g0164 a0001c0001t0001g0202 a0001c0001t0001g0203 others(89): Show |
118 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.426+336C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255623 | |||||||
chr11:86255705 | C | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.426+418C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255705 | |||||||
chr11:86255747 | T | C | 1 | a0001c0002t0001g0199 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.426+460T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255747 | |||||||
chr11:86255873 | G | T | 1 | a0001c0002t0001g0194 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.427-514G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255873 | |||||||
chr11:86255908 | C | G | 1 | a0001c0002t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.427-479C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255908 | |||||||
chr11:86255918 | T | TA | 3 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0267 |
3 | NA18952.hp1 NA18972.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.427-465dupA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 86255918 | ||||||
chr11:86255933 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.427-454T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255933 | |||||||
chr11:86256022 | A | G | 90 | a0001c0001t0001g0164 a0001c0002t0001g0002 a0001c0002t0001g0005 others(87): Show |
116 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.427-365A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86256022 | |||||||
chr11:86256256 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0041 others(53): Show |
72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.427-131A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86256256 | |||||||
chr11:86256545 | T | G | 1 | a0001c0002t0001g0168 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.552+33T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256545 | |||||||
chr11:86256604 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.552+92T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256604 | |||||||
chr11:86256610 | A | C | 1 | a0001c0001t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.552+98A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256610 | |||||||
chr11:86256628 | A | G | 4 | a0001c0001t0001g0085 a0001c0002t0001g0260 a0001c0002t0001g0265 others(1): Show |
4 | HG01258.hp1 HG02273.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+116A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256628 | |||||||
chr11:86256667 | G | A | 89 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0010 others(86): Show |
115 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.552+155G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256667 | |||||||
chr11:86256719 | A | C | 1 | a0001c0001t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.552+207A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256719 | |||||||
chr11:86256900 | G | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.552+388G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256900 | |||||||
chr11:86256910 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.552+398A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256910 | |||||||
chr11:86256995 | C | T | 92 | a0001c0001t0001g0164 a0001c0001t0001g0202 a0001c0001t0001g0203 others(89): Show |
118 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.552+483C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256995 | |||||||
chr11:86257003 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA18612.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.552+491C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257003 | |||||||
chr11:86257031 | G | A | 1 | a0001c0002t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.553-484G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257031 | |||||||
chr11:86257122 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.553-393G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257122 | |||||||
chr11:86257185 | T | TTG | 12 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0027 others(9): Show |
16 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.553-298_553-297dup others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | ||||||
chr11:86257185 | T | TTGTG | 3 | a0001c0001t0001g0129 a0001c0001t0001g0204 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.553-300_553-297dup others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | ||||||
chr11:86257185 | T | TTGTGTGT others(1): Show |
14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0121 others(11): Show |
16 | HG01074.hp2 HG01884.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.553-304_553-297dup others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | ||||||
chr11:86257185 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG02273.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.553-306_553-297dup others(10): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | ||||||
chr11:86257185 | TTG | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0032 others(125): Show |
171 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.553-298_553-297del others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | ||||||
chr11:86257185 | TTGTG | T | 14 | a0001c0001t0001g0164 a0001c0001t0001g0202 a0001c0001t0001g0203 others(11): Show |
14 | HG01192.hp2 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-300_553-297del others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | ||||||
chr11:86257185 | TTGTGTGT others(1): Show |
T | 26 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
32 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(29): Show |
intron_variant | MODIFIER | c.553-304_553-297del others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | ||||||
chr11:86257323 | C | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.553-192C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257323 | |||||||
chr11:86257340 | CT | C | 47 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(44): Show |
55 | HG00408.hp2 HG00558.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.553-157delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257340 | ||||||
chr11:86257358 | T | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.553-157T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257358 | |||||||
chr11:86257439 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.553-76C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257439 | |||||||
chr11:86257697 | A | G | 1 | a0001c0002t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.634+101A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257697 | |||||||
chr11:86257706 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.634+110A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257706 | |||||||
chr11:86257710 | G | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+114G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257710 | |||||||
chr11:86257794 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.634+198C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257794 | |||||||
chr11:86257821 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.634+225G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257821 | |||||||
chr11:86258075 | T | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0071 others(14): Show |
22 | HG01099.hp1 HG01255.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.634+479T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258075 | |||||||
chr11:86258163 | TA | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0041 others(53): Show |
72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.634+575delA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86258163 | ||||||
chr11:86258505 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.634+909C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258505 | |||||||
chr11:86258536 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.634+940C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258536 | |||||||
chr11:86258543 | C | T | 89 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0010 others(86): Show |
115 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.634+947C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258543 | |||||||
chr11:86258554 | G | GTTTT | 13 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0140 others(10): Show |
15 | HG00438.hp2 HG02056.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.634+958_634+959ins others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258554 | |||||||
chr11:86258554 | G | GTTTTT | 10 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0142 others(7): Show |
13 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.634+958_634+959ins others(5): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258554 | |||||||
chr11:86258554 | G | T | 3 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0001c0002t0001g0247 |
3 | HG01106.hp1 HG01978.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.634+958G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258554 | |||||||
chr11:86258555 | G | GT | 41 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(38): Show |
44 | HG01074.hp2 HG01884.hp2 HG02056.hp1 others(41): Show |
intron_variant | MODIFIER | c.634+976dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86258555 | ||||||
chr11:86258555 | G | T | 26 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
32 | HG00408.hp2 HG00438.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.634+959G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258555 | |||||||
chr11:86258762 | G | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(22): Show |
31 | HG00408.hp2 HG00438.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.634+1166G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258762 | |||||||
chr11:86258786 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.634+1190C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258786 | |||||||
chr11:86258847 | C | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
4 | HG02976.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1251C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258847 | |||||||
chr11:86258858 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0157 |
2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.634+1262T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258858 | |||||||
chr11:86259129 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0089 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.634+1533A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259129 | |||||||
chr11:86259223 | T | TAAAAATC others(312): Show |
40 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0041 others(37): Show |
55 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.634+1643_634+1644i others(321): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259223 | ||||||
chr11:86259223 | T | TAAAAATC others(313): Show |
13 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0208 others(10): Show |
14 | HG01069.hp2 HG01123.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+1643_634+1644i others(322): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259223 | ||||||
chr11:86259223 | T | TAAAAATC others(314): Show |
1 | a0001c0001t0003g0219 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.634+1643_634+1644i others(323): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259223 | ||||||
chr11:86259223 | T | TAAAAATC others(312): Show |
1 | a0001c0001t0001g0231 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.634+1643_634+1644i others(321): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259223 | ||||||
chr11:86259228 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+1632A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259228 | |||||||
chr11:86259251 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.634+1655G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259251 | |||||||
chr11:86259392 | T | TG | 142 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0030 others(139): Show |
177 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.634+1797dupG | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259392 | ||||||
chr11:86259409 | T | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+1813T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259409 | |||||||
chr11:86259492 | G | T | 1 | a0001c0002t0001g0192 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.634+1896G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259492 | |||||||
chr11:86259514 | C | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+1918C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259514 | |||||||
chr11:86259515 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.634+1919C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259515 | |||||||
chr11:86259606 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(199): Show |
254 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.634+2010T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259606 | |||||||
chr11:86259834 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.634+2238A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259834 | |||||||
chr11:86259998 | C | A | 1 | a0001c0002t0001g0262 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.634+2402C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259998 | |||||||
chr11:86260097 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+2501A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260097 | |||||||
chr11:86260176 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.634+2580A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260176 | |||||||
chr11:86260280 | T | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+2684T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260280 | |||||||
chr11:86260380 | C | G | 1 | a0001c0002t0001g0253 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.634+2784C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260380 | |||||||
chr11:86260403 | A | AT | 203 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(200): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.634+2813dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86260403 | ||||||
chr11:86260421 | G | A | 1 | a0001c0002t0001g0262 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.634+2825G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260421 | |||||||
chr11:86260516 | A | ACTGCACC others(4): Show |
203 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(200): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.634+2924_634+2925i others(13): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86260516 | ||||||
chr11:86260695 | A | C | 1 | a0001c0001t0001g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.634+3099A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260695 | |||||||
chr11:86260823 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.634+3227T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260823 | |||||||
chr11:86260824 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.634+3228A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260824 | |||||||
chr11:86260825 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.634+3229T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260825 | |||||||
chr11:86260844 | A | T | 1 | a0001c0002t0001g0163 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.634+3248A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260844 | |||||||
chr11:86260900 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.635-3272G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260900 | |||||||
chr11:86260917 | CT | C | 12 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0115 others(9): Show |
14 | HG02572.hp1 HG02809.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-3243delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86260917 | ||||||
chr11:86260992 | T | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
10 | HG02572.hp1 HG02809.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.635-3180T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260992 | |||||||
chr11:86261048 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.635-3124C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261048 | |||||||
chr11:86261090 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.635-3082A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261090 | |||||||
chr11:86261120 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0139 a0001c0001t0001g0296 |
6 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-3052G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261120 | |||||||
chr11:86261152 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.635-3020C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261152 | |||||||
chr11:86261200 | A | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0062 others(4): Show |
9 | NA18959.hp2 NA18967.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-2972A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261200 | |||||||
chr11:86261254 | C | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.635-2918C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261254 | |||||||
chr11:86261274 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.635-2898C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261274 | |||||||
chr11:86261404 | GC | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.635-2764delC | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86261404 | ||||||
chr11:86261436 | C | T | 94 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0140 others(91): Show |
121 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.635-2736C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261436 | |||||||
chr11:86261733 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.635-2439G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261733 | |||||||
chr11:86261752 | C | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.635-2420C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261752 | |||||||
chr11:86261897 | T | C | 142 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0030 others(139): Show |
177 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.635-2275T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261897 | |||||||
chr11:86261963 | A | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.635-2209A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261963 | |||||||
chr11:86262176 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.635-1996C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262176 | |||||||
chr11:86262547 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.635-1625C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262547 | |||||||
chr11:86262578 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0205 |
2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.635-1594A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262578 | |||||||
chr11:86262599 | C | T | 2 | a0001c0001t0001g0164 a0001c0002t0001g0200 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.635-1573C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262599 | |||||||
chr11:86262673 | G | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.635-1499G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262673 | |||||||
chr11:86262813 | C | CT | 46 | a0001c0001t0001g0032 a0001c0001t0001g0054 a0001c0001t0001g0136 others(43): Show |
59 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.635-1346dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86262813 | ||||||
chr11:86262813 | C | CTT | 55 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0140 others(52): Show |
70 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.635-1347_635-1346d others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86262813 | ||||||
chr11:86262827 | C | T | 142 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0030 others(139): Show |
177 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.635-1345C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262827 | |||||||
chr11:86262960 | C | T | 5 | a0001c0002t0001g0176 a0001c0002t0001g0180 a0001c0002t0001g0190 others(2): Show |
5 | HG00544.hp2 NA18941.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-1212C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262960 | |||||||
chr11:86263033 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0079 |
2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.635-1139C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263033 | |||||||
chr11:86263046 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.635-1126G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263046 | |||||||
chr11:86263150 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.635-1022T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263150 | |||||||
chr11:86263354 | G | C | 1 | a0001c0002t0001g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.635-818G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263354 | |||||||
chr11:86263547 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.635-625A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263547 | |||||||
chr11:86263932 | T | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.635-240T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263932 | |||||||
chr11:86264118 | G | A | 1 | a0001c0002t0001g0170 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.635-54G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86264118 | |||||||
chr11:86264295 | A | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0119 others(1): Show |
8 | HG00140.hp2 HG00280.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.726+32A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264295 | |||||||
chr11:86264334 | C | T | 1 | a0001c0002t0001g0162 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.726+71C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264334 | |||||||
chr11:86264439 | A | ATATT | 116 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0031 others(113): Show |
145 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.726+190_726+193dup others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 86264439 | ||||||
chr11:86264633 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.726+370G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264633 | |||||||
chr11:86264730 | A | G | 18 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0140 others(15): Show |
23 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.726+467A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264730 | |||||||
chr11:86264851 | C | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0069 a0001c0001t0001g0080 others(3): Show |
7 | HG00323.hp2 HG00738.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.726+588C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264851 | |||||||
chr11:86265169 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.726+906A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265169 | |||||||
chr11:86265320 | C | G | 1 | a0001c0001t0001g0044 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.727-763C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265320 | |||||||
chr11:86265439 | G | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.727-644G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265439 | |||||||
chr11:86265495 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.727-588C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265495 | |||||||
chr11:86265990 | A | T | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.727-93A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265990 | |||||||
chr11:86266075 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
splice_region_variant&intron_variant | LOW | c.727-8G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86266075 | |||||||
chr11:86266497 | T | C | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.860+281T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86266497 | |||||||
chr11:86266849 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0148 |
3 | HG01496.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.860+633C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86266849 | |||||||
chr11:86266873 | T | G | 1 | a0001c0001t0001g0101 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.860+657T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86266873 | |||||||
chr11:86266958 | C | T | 142 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0030 others(139): Show |
177 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.860+742C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86266958 | |||||||
chr11:86267144 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.860+928A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267144 | |||||||
chr11:86267156 | G | A | 1 | a0001c0002t0001g0182 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.860+940G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267156 | |||||||
chr11:86267218 | A | G | 1 | a0001c0002t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.860+1002A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267218 | |||||||
chr11:86267394 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.861-1062A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267394 | |||||||
chr11:86267622 | C | T | 142 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0030 others(139): Show |
177 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.861-834C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267622 | |||||||
chr11:86267689 | C | G | 1 | a0001c0002t0001g0189 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.861-767C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267689 | |||||||
chr11:86267692 | G | C | 142 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0030 others(139): Show |
177 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.861-764G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267692 | |||||||
chr11:86267766 | A | AT | 11 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0068 others(8): Show |
12 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-670dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | ||||||
chr11:86267766 | A | ATT | 8 | a0001c0001t0001g0032 a0001c0001t0001g0136 a0001c0001t0001g0137 others(5): Show |
9 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.861-671_861-670dup others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | ||||||
chr11:86267766 | A | ATTT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0041 others(52): Show |
72 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.861-672_861-670dup others(3): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | ||||||
chr11:86267766 | A | ATTTT | 126 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0030 others(123): Show |
160 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.861-673_861-670dup others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | ||||||
chr11:86267766 | A | ATTTTT | 13 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0150 others(10): Show |
13 | HG02145.hp1 HG02970.hp1 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.861-674_861-670dup others(5): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | ||||||
chr11:86267821 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.861-635G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267821 | |||||||
chr11:86267932 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.861-524G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267932 | |||||||
chr11:86267968 | G | C | 115 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0031 others(112): Show |
144 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.861-488G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267968 | |||||||
chr11:86268007 | TG | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.861-448delG | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86268007 | |||||||
chr11:86268153 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0231 a0001c0001t0004g0230 |
4 | HG02615.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-303C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86268153 | |||||||
chr11:86268194 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.861-262C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86268194 | |||||||
chr11:86268228 | T | G | 97 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0140 others(94): Show |
124 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.861-228T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86268228 | |||||||
chr11:86268591 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.966+30C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86268591 | |||||||
chr11:86268594 | C | CGT | 32 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(29): Show |
40 | HG00558.hp1 HG01074.hp2 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.966+64_966+65dupGT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | ||||||
chr11:86268594 | C | CGTGT | 68 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(65): Show |
86 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.966+62_966+65dupGT others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | ||||||
chr11:86268594 | C | CGTGTGT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0053 a0001c0001t0001g0066 others(9): Show |
17 | HG02027.hp2 HG02080.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.966+60_966+65dupGT others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | ||||||
chr11:86268594 | C | CGTGTGTG others(1): Show |
49 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0042 others(46): Show |
62 | HG00140.hp1 HG00323.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.966+58_966+65dupGT others(6): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | ||||||
chr11:86268594 | C | CGTGTGTG others(3): Show |
6 | a0001c0001t0001g0157 a0001c0001t0001g0208 a0001c0001t0001g0214 others(3): Show |
6 | HG00639.hp1 HG01175.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+56_966+65dupGT others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | ||||||
chr11:86268594 | C | CGTGTGTG others(5): Show |
2 | a0001c0001t0001g0203 a0001c0001t0001g0231 |
2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.966+54_966+65dupGT others(10): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | ||||||
chr11:86268594 | C | CGTGTGTG others(15): Show |
1 | a0001c0002t0001g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.966+44_966+65dupGT others(20): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | ||||||
chr11:86268594 | CGT | C | 41 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0091 others(38): Show |
55 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.966+64_966+65delGT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | ||||||
chr11:86268601 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0048 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.966+49_966+50insAT others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268601 | ||||||
chr11:86268623 | GTGTA | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0134 |
3 | HG03471.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.966+66_966+69delAT others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268623 | ||||||
chr11:86268624 | TGTATGTG others(5): Show |
T | 1 | a0001c0001t0001g0049 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.966+65_966+76delTA others(10): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268624 | ||||||
chr11:86268627 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
21 | HG01074.hp2 HG01884.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.966+66A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86268627 | |||||||
chr11:86268636 | C | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0121 others(14): Show |
19 | HG01074.hp2 HG01884.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.966+75C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86268636 | |||||||
chr11:86268910 | T | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
12 | HG00140.hp2 HG00280.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+349T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86268910 | |||||||
chr11:86269031 | C | T | 142 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0030 others(139): Show |
177 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.966+470C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269031 | |||||||
chr11:86269115 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.966+554G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269115 | |||||||
chr11:86269193 | A | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
25 | HG00741.hp1 HG01192.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.966+632A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269193 | |||||||
chr11:86269311 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.966+750C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269311 | |||||||
chr11:86269432 | A | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0099 |
2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.966+871A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269432 | |||||||
chr11:86269773 | A | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0079 others(1): Show |
6 | HG02258.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+1212A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269773 | |||||||
chr11:86269786 | C | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0002t0001g0005 others(49): Show |
66 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.966+1225C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269786 | |||||||
chr11:86269895 | C | G | 1 | a0001c0002t0001g0191 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.966+1334C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269895 | |||||||
chr11:86269915 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+1354C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269915 | |||||||
chr11:86269916 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(200): Show |
255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.966+1355A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269916 | |||||||
chr11:86269919 | T | G | 1 | a0001c0002t0001g0240 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.966+1358T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269919 | |||||||
chr11:86270126 | A | G | 1 | a0001c0002t0001g0186 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.966+1565A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270126 | |||||||
chr11:86270213 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.966+1652T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270213 | |||||||
chr11:86270272 | C | CTTAT | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.966+1715_966+1718d others(6): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86270272 | ||||||
chr11:86270293 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.966+1732C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270293 | |||||||
chr11:86270355 | GT | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
363 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(360): Show |
intron_variant | MODIFIER | c.966+1810delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86270355 | ||||||
chr11:86270355 | GTT | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0062 others(6): Show |
12 | HG01496.hp2 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.966+1809_966+1810d others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86270355 | ||||||
chr11:86270545 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0228 |
2 | HG01070.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.966+1984A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270545 | |||||||
chr11:86270835 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.966+2274G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270835 | |||||||
chr11:86271149 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.966+2588C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271149 | |||||||
chr11:86271269 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.966+2708A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271269 | |||||||
chr11:86271271 | G | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.966+2710G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271271 | |||||||
chr11:86271628 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.966+3067G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271628 | |||||||
chr11:86271665 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(30): Show |
46 | HG00140.hp1 HG01069.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.966+3104T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271665 | |||||||
chr11:86271941 | C | CT | 39 | a0001c0001t0001g0206 a0001c0002t0001g0002 a0001c0002t0001g0021 others(36): Show |
52 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.966+3390dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86271941 | ||||||
chr11:86272056 | A | ATTTTGTT others(896): Show |
13 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(10): Show |
15 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(12): Show |
intron_variant | MODIFIER | c.966+3499_966+3500i others(905): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | ||||||
chr11:86272056 | A | ATTTTGTT others(897): Show |
1 | a0001c0001t0001g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.966+3499_966+3500i others(906): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | ||||||
chr11:86272056 | A | ATTTTGTT others(897): Show |
3 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02976.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.966+3499_966+3500i others(906): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | ||||||
chr11:86272056 | A | ATTTTGTT others(898): Show |
1 | a0001c0001t0001g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.966+3499_966+3500i others(907): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | ||||||
chr11:86272056 | A | ATTTTTTT others(894): Show |
1 | a0001c0001t0001g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | ||||||
chr11:86272056 | A | ATTTTTTT others(895): Show |
1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(904): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | ||||||
chr11:86272057 | T | TTTTTTTT others(892): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0082 others(8): Show |
16 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.966+3519_966+3520i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272057 | T | TTTTTTTT others(893): Show |
1 | a0001c0001t0001g0096 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272057 | T | TTTTTTTT others(893): Show |
37 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
51 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272057 | T | TTTTTTTT others(894): Show |
1 | a0001c0002t0001g0274 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272057 | T | TTTTTTTT others(894): Show |
1 | a0001c0001t0001g0092 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272057 | T | TTTTTTTT others(894): Show |
38 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
57 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272057 | T | TTTTTTTT others(894): Show |
1 | a0001c0001t0001g0008 | 4 | HG01099.hp2 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272057 | T | TTTTTTTT others(895): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0119 |
2 | HG02280.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.966+3514_966+3515i others(904): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272057 | T | TTTTTTTT others(896): Show |
1 | a0001c0001t0001g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(905): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272057 | T | TTTTTTTT others(897): Show |
1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(906): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | ||||||
chr11:86272058 | T | TTTTTTTT others(890): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.966+3513_966+3514i others(899): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(892): Show |
1 | a0001c0002t0001g0277 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(892): Show |
1 | a0001c0002t0001g0187 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(892): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0286 |
3 | HG01256.hp2 HG01258.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.966+3514_966+3515i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(893): Show |
1 | a0001c0001t0001g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(893): Show |
32 | a0001c0001t0001g0206 a0001c0002t0001g0002 a0001c0002t0001g0021 others(29): Show |
44 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(893): Show |
1 | a0001c0002t0001g0039 | 2 | NA18977.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(893): Show |
45 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0140 others(42): Show |
59 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(893): Show |
1 | a0001c0002t0001g0172 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(893): Show |
10 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(7): Show |
10 | HG00323.hp1 HG00639.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(893): Show |
38 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(35): Show |
52 | HG00140.hp1 HG01069.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(894): Show |
4 | a0001c0002t0001g0249 a0001c0002t0001g0256 a0001c0002t0001g0258 others(1): Show |
4 | HG02074.hp1 HG03942.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(894): Show |
6 | a0001c0001t0001g0164 a0001c0002t0001g0178 a0001c0002t0001g0183 others(3): Show |
6 | HG01981.hp2 HG03130.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(894): Show |
1 | a0001c0001t0001g0291 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(894): Show |
12 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0050 others(9): Show |
14 | HG01175.hp2 HG01517.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(894): Show |
1 | a0001c0002t0001g0163 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(895): Show |
18 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(15): Show |
24 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(904): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(895): Show |
1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(904): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272058 | T | TTTTTTTT others(896): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0155 |
3 | HG02027.hp1 NA19066.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.966+3514_966+3515i others(905): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | ||||||
chr11:86272059 | T | TTTTTTTT others(891): Show |
1 | a0001c0002t0001g0171 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(900): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272059 | ||||||
chr11:86272059 | T | TTTTTTTT others(892): Show |
1 | a0001c0002t0001g0271 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272059 | ||||||
chr11:86272061 | T | TTTTTTTT others(890): Show |
1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(899): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272061 | ||||||
chr11:86272076 | G | A | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.966+3515G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272076 | |||||||
chr11:86272092 | C | G | 94 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0140 others(91): Show |
121 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.966+3531C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272092 | |||||||
chr11:86272118 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.966+3557C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272118 | |||||||
chr11:86272218 | C | T | 2 | a0001c0001t0001g0206 a0001c0002t0001g0255 |
2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.966+3657C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272218 | |||||||
chr11:86272279 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.966+3718C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272279 | |||||||
chr11:86272304 | T | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.966+3743T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272304 | |||||||
chr11:86272317 | C | T | 5 | a0001c0002t0001g0047 a0001c0002t0001g0252 a0001c0002t0001g0253 others(2): Show |
6 | HG02056.hp1 NA18952.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3756C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272317 | |||||||
chr11:86272338 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+3777G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272338 | |||||||
chr11:86272406 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.966+3845C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272406 | |||||||
chr11:86272455 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0078 |
2 | HG03831.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.966+3894A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272455 | |||||||
chr11:86272556 | G | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.966+3995G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272556 | |||||||
chr11:86272565 | T | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0095 |
2 | NA19068.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.966+4004T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272565 | |||||||
chr11:86272661 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0228 |
2 | HG01070.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.966+4100A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272661 | |||||||
chr11:86272907 | T | A | 1 | a0001c0002t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.967-4073T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272907 | |||||||
chr11:86272927 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.967-4053T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272927 | |||||||
chr11:86273148 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.967-3832C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273148 | |||||||
chr11:86273257 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.967-3723A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273257 | |||||||
chr11:86273347 | T | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | NA18993.hp1 NA19003.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.967-3633T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273347 | |||||||
chr11:86273694 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.967-3286T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273694 | |||||||
chr11:86273880 | T | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-3100T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273880 | |||||||
chr11:86273905 | A | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0057 |
3 | HG00741.hp1 HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.967-3075A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273905 | |||||||
chr11:86274057 | A | G | 2 | a0001c0002t0001g0250 a0001c0002t0001g0273 |
2 | NA18950.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.967-2923A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274057 | |||||||
chr11:86274101 | CT | C | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(16): Show |
21 | HG01074.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.967-2866delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86274101 | ||||||
chr11:86274157 | T | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-2823T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274157 | |||||||
chr11:86274194 | T | G | 1 | a0001c0001t0001g0110 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.967-2786T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274194 | |||||||
chr11:86274203 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.967-2777T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274203 | |||||||
chr11:86274455 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.967-2525C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274455 | |||||||
chr11:86274488 | C | G | 1 | a0001c0001t0001g0207 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.967-2492C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274488 | |||||||
chr11:86274635 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0157 |
2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.967-2345C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274635 | |||||||
chr11:86274661 | G | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-2319G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274661 | |||||||
chr11:86274696 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0205 |
5 | HG00544.hp1 HG03209.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.967-2284C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274696 | |||||||
chr11:86274697 | C | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0251 |
3 | HG01346.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.967-2283C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274697 | |||||||
chr11:86274758 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-2222A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274758 | |||||||
chr11:86274811 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.967-2169G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274811 | |||||||
chr11:86275005 | A | G | 24 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(21): Show |
38 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.967-1975A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275005 | |||||||
chr11:86275070 | G | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1910G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275070 | |||||||
chr11:86275090 | T | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1890T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275090 | |||||||
chr11:86275202 | T | C | 2 | a0001c0002t0001g0264 a0001c0002t0001g0270 |
2 | HG01255.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.967-1778T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275202 | |||||||
chr11:86275203 | G | A | 2 | a0001c0002t0001g0264 a0001c0002t0001g0270 |
2 | HG01255.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.967-1777G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275203 | |||||||
chr11:86275367 | G | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1613G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275367 | |||||||
chr11:86275411 | C | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1569C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275411 | |||||||
chr11:86275476 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(225): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.967-1504G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275476 | |||||||
chr11:86275601 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.967-1379A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275601 | |||||||
chr11:86275618 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.967-1362C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275618 | |||||||
chr11:86275745 | T | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1235T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275745 | |||||||
chr11:86275846 | G | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.967-1134G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275846 | |||||||
chr11:86276022 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.967-958G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276022 | |||||||
chr11:86276146 | C | G | 18 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0140 others(15): Show |
23 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.967-834C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276146 | |||||||
chr11:86276488 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-492A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276488 | |||||||
chr11:86276548 | G | A | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0049 others(15): Show |
20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-432G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276548 | |||||||
chr11:86276563 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.967-417G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276563 | |||||||
chr11:86276776 | A | C | 30 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
40 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.967-204A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276776 | |||||||
chr11:86277184 | A | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0081 a0001c0001t0001g0099 |
4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+46A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 10/11 | chr11 | 86277184 | |||||||
chr11:86277585 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-333A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 10/11 | chr11 | 86277585 | |||||||
chr11:86277788 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1126-130G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 10/11 | chr11 | 86277788 | |||||||
chr11:86278001 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1199+10T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 11/11 | chr11 | 86278001 |