Item | Value |
---|---|
geneid | 2001 |
ensemblid | ENSG00000135374.11 |
hgncid | 3320 |
symbol | ELF5 |
name | E74 like ETS transcription factor 5 |
refseq_nuc | NM_001422.4 |
refseq_prot | NP_001413.1 |
ensembl_nuc | ENST00000257832.7 |
ensembl_prot | ENSP00000257832.3 |
mane_status | MANE Select |
chr | chr11 |
start | 34478791 |
end | 34513794 |
strand | - |
ver | v1.2 |
region | chr11:34478791-34513794 |
region5000 | chr11:34473791-34518794 |
regionname0 | ELF5_chr11_34478791_34513794 |
regionname5000 | ELF5_chr11_34473791_34518794 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 255 | 425 | 94 | 76 | 203 | 16 | 34 | 159 | ELF5_chr11_34473791_34518794 | ELF5 | MLDSV others(250): Show |
chr11 | 34473791 | 34518794 |
a0002 | 0/0 | 255 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | ELF5_chr11_34473791_34518794 | ELF5 | MLDSV others(250): Show |
chr11 | 34473791 | 34518794 |
a0003 | 0/0 | 255 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | MLDSV others(250): Show |
chr11 | 34473791 | 34518794 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 765 | 374 | 93 | 55 | 194 | 11 | 20 | ELF5_chr11_34473791_34518794 | ELF5 | ATGTT others(760): Show |
chr11 | 34473791 | 34518794 | ||
a0001c0002 | 0/1 | 765 | 51 | 1 | 21 | 9 | 5 | 14 | ELF5_chr11_34473791_34518794 | ELF5 | ATGTT others(760): Show |
chr11 | 34473791 | 34518794 | ||
a0002c0003 | 0/0 | 765 | 10 | 0 | 0 | 10 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | ATGTT others(760): Show |
chr11 | 34473791 | 34518794 | ||
a0003c0004 | 0/0 | 765 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | ATGTT others(760): Show |
chr11 | 34473791 | 34518794 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2318 | 140 | 7 | 30 | 84 | 7 | 12 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2313): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0002 | 0/0 | 2317 | 73 | 12 | 4 | 55 | 2 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0003 | 1/0 | 2317 | 64 | 12 | 12 | 32 | 2 | 5 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0005 | 0/0 | 2317 | 45 | 41 | 4 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0006 | 0/0 | 2319 | 15 | 0 | 5 | 10 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2314): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0007 | 0/0 | 2318 | 8 | 8 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2313): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0008 | 0/0 | 2318 | 6 | 0 | 0 | 6 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2313): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0009 | 0/0 | 2317 | 6 | 3 | 0 | 3 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0010 | 0/0 | 2317 | 5 | 5 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0011 | 0/0 | 2317 | 2 | 2 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0012 | 0/0 | 2318 | 2 | 2 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2313): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0013 | 0/0 | 2318 | 2 | 0 | 0 | 0 | 0 | 2 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2313): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0014 | 0/0 | 2317 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0015 | 0/0 | 2317 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0017 | 0/0 | 2318 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2313): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0018 | 0/0 | 2319 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2314): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0019 | 0/0 | 2317 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0001t0020 | 0/0 | 2318 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2313): Show |
chr11 | 34473791 | 34518794 |
a0001c0002t0004 | 0/1 | 2317 | 50 | 1 | 20 | 9 | 5 | 14 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0001c0002t0016 | 0/0 | 2317 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2312): Show |
chr11 | 34473791 | 34518794 |
a0002c0003t0001 | 0/0 | 2318 | 10 | 0 | 0 | 10 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2313): Show |
chr11 | 34473791 | 34518794 |
a0003c0004t0008 | 0/0 | 2318 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | GTCAC others(2313): Show |
chr11 | 34473791 | 34518794 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0031 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0002 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0026 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0008g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0009g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0009g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0010g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0011g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0011g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0012g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0013g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0013g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0014g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0015g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0017g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0018g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0019g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0001t0020g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0006 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0020 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0055 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0001c0002t0016g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0002c0003t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0002c0003t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
a0003c0004t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0264 | EUR | GBR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | GBR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | GBR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0260 | EUR | FIN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00280 | hp2 | a0001 | c0002 | t0004 | g0161 | EUR | FIN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00323 | hp1 | a0001 | c0002 | t0004 | g0094 | EUR | FIN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | FIN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00544 | hp1 | a0001 | c0001 | t0006 | g0079 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00609 | hp1 | a0001 | c0001 | t0006 | g0173 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00621 | hp2 | a0001 | c0002 | t0004 | g0111 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0051 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00642 | hp1 | a0001 | c0002 | t0004 | g0021 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00733 | hp2 | a0001 | c0002 | t0004 | g0093 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00735 | hp1 | a0001 | c0002 | t0004 | g0195 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0316 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00741 | hp1 | a0001 | c0002 | t0004 | g0276 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01070 | hp2 | a0001 | c0002 | t0004 | g0021 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01071 | hp2 | a0001 | c0002 | t0004 | g0021 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01081 | hp2 | a0001 | c0002 | t0004 | g0119 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0050 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0261 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01243 | hp1 | a0001 | c0002 | t0004 | g0051 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0240 | AMR | PUR | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01257 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01258 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01358 | hp1 | a0001 | c0002 | t0016 | g0263 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01358 | hp2 | a0001 | c0002 | t0004 | g0277 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0053 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01496 | hp1 | a0001 | c0002 | t0004 | g0055 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01515 | hp2 | a0001 | c0002 | t0004 | g0319 | EUR | IBS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0294 | EUR | IBS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01517 | hp2 | a0001 | c0002 | t0004 | g0055 | EUR | IBS | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0186 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0259 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0180 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01928 | hp1 | a0001 | c0002 | t0004 | g0020 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0026 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01978 | hp2 | a0001 | c0002 | t0004 | g0112 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0215 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01993 | hp2 | a0001 | c0002 | t0004 | g0066 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02004 | hp2 | a0001 | c0002 | t0004 | g0303 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02015 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02040 | hp1 | a0001 | c0002 | t0004 | g0061 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02055 | hp1 | a0001 | c0001 | t0017 | g0306 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0077 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02129 | hp1 | a0001 | c0001 | t0006 | g0208 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0209 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0317 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0026 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0036 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0265 | AMR | PEL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02451 | hp1 | a0001 | c0001 | t0010 | g0302 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02523 | hp2 | a0001 | c0001 | t0006 | g0102 | EAS | KHV | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0300 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02622 | hp1 | a0001 | c0001 | t0012 | g0052 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0052 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02683 | hp1 | a0001 | c0002 | t0004 | g0020 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02717 | hp1 | a0001 | c0001 | t0010 | g0288 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02723 | hp2 | a0001 | c0001 | t0009 | g0103 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02738 | hp1 | a0001 | c0001 | t0013 | g0097 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02738 | hp2 | a0001 | c0002 | t0004 | g0314 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0292 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0272 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0311 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0249 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02965 | hp1 | a0001 | c0001 | t0010 | g0301 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0299 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03017 | hp1 | a0001 | c0001 | t0013 | g0128 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0296 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0219 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0254 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0321 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0286 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03491 | hp1 | a0001 | c0002 | t0004 | g0089 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | ESN | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0308 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03579 | hp2 | a0001 | c0001 | t0010 | g0222 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03688 | hp2 | a0001 | c0002 | t0004 | g0006 | SAS | STU | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03704 | hp2 | a0001 | c0002 | t0004 | g0269 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0113 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03927 | hp1 | a0001 | c0002 | t0004 | g0016 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03927 | hp2 | a0001 | c0002 | t0004 | g0117 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03942 | hp1 | a0001 | c0002 | t0004 | g0060 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03942 | hp2 | a0001 | c0002 | t0004 | g0020 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | STU | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG04184 | hp2 | a0001 | c0001 | t0018 | g0101 | SAS | BEB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG04199 | hp1 | a0001 | c0002 | t0004 | g0138 | SAS | STU | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG04199 | hp2 | a0001 | c0002 | t0004 | g0255 | SAS | STU | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG04228 | hp2 | a0001 | c0002 | t0004 | g0141 | SAS | STU | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0320 | AFR | YRI | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0237 | AFR | YRI | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CHB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18612 | hp2 | a0001 | c0001 | t0009 | g0043 | EAS | CHB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | YRI | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | YRI | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18941 | hp2 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18947 | hp2 | a0001 | c0001 | t0014 | g0210 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18949 | hp1 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18952 | hp2 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18957 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18957 | hp2 | a0001 | c0001 | t0019 | g0147 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18959 | hp2 | a0001 | c0001 | t0020 | g0245 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18963 | hp1 | a0001 | c0002 | t0004 | g0185 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18964 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18968 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18970 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18971 | hp2 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18972 | hp2 | a0002 | c0003 | t0001 | g0153 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18978 | hp2 | a0001 | c0001 | t0015 | g0250 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18983 | hp1 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18985 | hp2 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18986 | hp2 | a0001 | c0002 | t0004 | g0027 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18994 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18997 | hp1 | a0001 | c0002 | t0004 | g0027 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19002 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19003 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19004 | hp2 | a0001 | c0001 | t0008 | g0155 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19005 | hp2 | a0001 | c0001 | t0009 | g0043 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19012 | hp2 | a0001 | c0002 | t0004 | g0016 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | LWK | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0262 | AFR | LWK | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | LWK | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | LWK | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19056 | hp2 | a0003 | c0004 | t0008 | g0121 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19079 | hp2 | a0001 | c0002 | t0004 | g0027 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19082 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19086 | hp2 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19087 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0304 | AFR | YRI | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0230 | AFR | YRI | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0242 | AFR | ASW | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | ASW | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0267 | EUR | TSI | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | GIH | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0016 | SAS | GIH | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG01123 | hp2 | a0001 | c0002 | t0004 | g0278 | AMR | CLM | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0295 | AFR | MSL | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | USA | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | USA | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA18955 | hp2 | a0001 | c0001 | t0008 | g0203 | EAS | JPT | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0241 | AFR | USA | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | USA | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
homoSapiens | chm13v2 | a0001 | c0002 | t0004 | g0075 | REF | REF | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0116 | REF | REF | ELF5_chr11_34473791_34518794 | ELF5 | chr11 | 34473791 | 34518794 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:34480923 | G | C | 1 | a0002 | 10 | NA18941.hp2 NA18957.hp1 NA18964.hp2 others(7): Show |
missense_variant | MODERATE | c.520C>G | p.Leu174Val | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 6/7 | 642/2317 | 520/768 | 174/255 | chr11 | 34480923 | |||
chr11:34493613 | G | A | 1 | a0003 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.221C>T | p.Thr74Ile | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/7 | 343/2317 | 221/768 | 74/255 | chr11 | 34493613 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:34480798 | T | C | 1 | a0001c0002 | 50 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(47): Show |
synonymous_variant | LOW | c.645A>G | p.Thr215Thr | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 6/7 | 767/2317 | 645/768 | 215/255 | chr11 | 34480798 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:34478816 | C | T | 1 | a0001c0001t0012 | 2 | HG02622.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1402G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 1402 | chr11 | 34478816 | ||||||
chr11:34478884 | T | C | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(17): Show |
370 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(367): Show |
3_prime_UTR_variant | MODIFIER | c.*1334A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 1334 | chr11 | 34478884 | ||||||
chr11:34478928 | G | A | 2 | a0001c0001t0008 a0003c0004t0008 |
7 | NA18949.hp1 NA18952.hp2 NA18955.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1290C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 1290 | chr11 | 34478928 | ||||||
chr11:34479003 | G | A | 1 | a0001c0001t0010 | 5 | HG02451.hp1 HG02717.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1215C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 1215 | chr11 | 34479003 | ||||||
chr11:34479019 | G | C | 2 | a0001c0002t0004 a0001c0002t0016 |
50 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1199C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 1199 | chr11 | 34479019 | ||||||
chr11:34479139 | C | T | 1 | a0001c0001t0015 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1079G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 1079 | chr11 | 34479139 | ||||||
chr11:34479140 | G | A | 8 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(5): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1078C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 1078 | chr11 | 34479140 | ||||||
chr11:34479181 | A | G | 1 | a0001c0001t0014 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1037T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 1037 | chr11 | 34479181 | ||||||
chr11:34479251 | T | A | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(17): Show |
370 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(367): Show |
3_prime_UTR_variant | MODIFIER | c.*967A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 967 | chr11 | 34479251 | ||||||
chr11:34479362 | T | G | 1 | a0001c0001t0017 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*856A>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 856 | chr11 | 34479362 | ||||||
chr11:34479445 | G | T | 1 | a0001c0001t0011 | 2 | HG02896.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*773C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 773 | chr11 | 34479445 | ||||||
chr11:34479450 | T | C | 1 | a0001c0001t0011 | 2 | HG02896.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*768A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 768 | chr11 | 34479450 | ||||||
chr11:34479517 | C | A | 4 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0015 others(1): Show |
76 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*701G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 701 | chr11 | 34479517 | ||||||
chr11:34479605 | G | A | 1 | a0001c0002t0016 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*613C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 613 | chr11 | 34479605 | ||||||
chr11:34479619 | T | C | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(17): Show |
370 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(367): Show |
3_prime_UTR_variant | MODIFIER | c.*599A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 599 | chr11 | 34479619 | ||||||
chr11:34479663 | T | C | 2 | a0001c0001t0013 a0001c0001t0018 |
3 | HG02738.hp1 HG03017.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*555A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 555 | chr11 | 34479663 | ||||||
chr11:34479688 | C | CA | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(6): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*529dupT | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 529 | chr11 | 34479688 | ||||||
chr11:34479688 | C | CAA | 2 | a0001c0001t0006 a0001c0001t0018 |
16 | HG00544.hp1 HG00609.hp1 HG01934.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*528_*529dupTT | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 529 | chr11 | 34479688 | ||||||
chr11:34480049 | A | G | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(16): Show |
369 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(366): Show |
3_prime_UTR_variant | MODIFIER | c.*169T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 7/7 | 169 | chr11 | 34480049 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:34480389 | C | T | 1 | a0001c0001t0005g0321 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.672-75G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 6/6 | chr11 | 34480389 | |||||||
chr11:34480495 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
202 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.672-181G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 6/6 | chr11 | 34480495 | |||||||
chr11:34480540 | C | T | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.672-226G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 6/6 | chr11 | 34480540 | |||||||
chr11:34481004 | G | A | 5 | a0001c0001t0002g0181 a0001c0001t0002g0183 a0001c0001t0002g0223 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.476-37C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481004 | |||||||
chr11:34481306 | G | A | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.476-339C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481306 | |||||||
chr11:34481435 | A | C | 1 | a0001c0001t0003g0265 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.476-468T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481435 | |||||||
chr11:34481447 | C | T | 1 | a0001c0001t0003g0059 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.476-480G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481447 | |||||||
chr11:34481499 | C | T | 2 | a0001c0001t0006g0079 a0001c0001t0006g0100 |
2 | HG00544.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.476-532G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481499 | |||||||
chr11:34481638 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.476-671G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481638 | |||||||
chr11:34481675 | C | T | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.476-708G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481675 | |||||||
chr11:34481707 | T | C | 1 | a0001c0001t0007g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.475+724A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481707 | |||||||
chr11:34481819 | A | G | 4 | a0001c0001t0005g0080 a0001c0001t0005g0106 a0001c0001t0005g0237 others(1): Show |
4 | HG02622.hp2 HG02886.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+612T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481819 | |||||||
chr11:34481922 | T | C | 38 | a0001c0001t0005g0030 a0001c0001t0005g0049 a0001c0001t0005g0050 others(35): Show |
44 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.475+509A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34481922 | |||||||
chr11:34482014 | G | A | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.475+417C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34482014 | |||||||
chr11:34482102 | C | A | 2 | a0001c0001t0005g0168 a0001c0001t0005g0308 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.475+329G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34482102 | |||||||
chr11:34482186 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | NA18939.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.475+245T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34482186 | |||||||
chr11:34482210 | C | T | 1 | a0001c0001t0017g0306 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.475+221G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34482210 | |||||||
chr11:34482246 | G | T | 60 | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0031 others(57): Show |
73 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.475+185C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34482246 | |||||||
chr11:34482273 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.475+158T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34482273 | |||||||
chr11:34482279 | C | T | 2 | a0001c0001t0002g0226 a0001c0001t0002g0312 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.475+152G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 5/6 | chr11 | 34482279 | |||||||
chr11:34482541 | G | A | 1 | a0001c0002t0016g0263 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.407-42C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34482541 | |||||||
chr11:34482627 | G | T | 2 | a0001c0001t0005g0256 a0001c0001t0005g0257 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.407-128C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34482627 | |||||||
chr11:34482745 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.407-246C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34482745 | |||||||
chr11:34482792 | T | C | 2 | a0001c0001t0011g0249 a0001c0001t0011g0304 |
2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.407-293A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34482792 | |||||||
chr11:34482981 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.407-482C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34482981 | |||||||
chr11:34483004 | T | C | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.407-505A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483004 | |||||||
chr11:34483056 | C | T | 2 | a0001c0001t0003g0059 a0001c0001t0003g0150 |
2 | NA18954.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.407-557G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483056 | |||||||
chr11:34483112 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
370 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(367): Show |
intron_variant | MODIFIER | c.407-613T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483112 | |||||||
chr11:34483144 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.407-645A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483144 | |||||||
chr11:34483164 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(128): Show |
184 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.407-665A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483164 | |||||||
chr11:34483165 | G | A | 4 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0005g0256 others(1): Show |
4 | HG01884.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-666C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483165 | |||||||
chr11:34483173 | C | T | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.407-674G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483173 | |||||||
chr11:34483201 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.407-702G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483201 | |||||||
chr11:34483282 | C | G | 2 | a0001c0001t0005g0168 a0001c0001t0005g0308 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.407-783G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483282 | |||||||
chr11:34483291 | C | T | 17 | a0001c0001t0005g0049 a0001c0001t0005g0080 a0001c0001t0005g0106 others(14): Show |
18 | HG01243.hp2 HG02145.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.407-792G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483291 | |||||||
chr11:34483655 | A | G | 1 | a0001c0001t0005g0239 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.407-1156T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483655 | |||||||
chr11:34483868 | T | TTACTG | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
377 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(374): Show |
intron_variant | MODIFIER | c.407-1374_407-1370d others(7): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483868 | |||||||
chr11:34483888 | C | G | 4 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0005g0256 others(1): Show |
4 | HG01884.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-1389G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483888 | |||||||
chr11:34483906 | A | G | 38 | a0001c0001t0005g0030 a0001c0001t0005g0049 a0001c0001t0005g0050 others(35): Show |
44 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.407-1407T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483906 | |||||||
chr11:34483988 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
82 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.407-1489T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483988 | |||||||
chr11:34483999 | C | A | 1 | a0001c0001t0002g0064 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.407-1500G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34483999 | |||||||
chr11:34484008 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.407-1509G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484008 | |||||||
chr11:34484021 | TACTA | T | 3 | a0001c0001t0002g0037 a0001c0001t0002g0176 a0001c0001t0002g0216 |
4 | HG02074.hp1 NA18991.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-1526_407-1523d others(6): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484021 | |||||||
chr11:34484044 | G | A | 14 | a0001c0001t0007g0130 a0001c0001t0007g0214 a0001c0001t0007g0219 others(11): Show |
17 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.407-1545C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484044 | |||||||
chr11:34484191 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0078 |
2 | HG01074.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.407-1692A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484191 | |||||||
chr11:34484229 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
370 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(367): Show |
intron_variant | MODIFIER | c.407-1730G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484229 | |||||||
chr11:34484252 | CATACT | C | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.407-1758_407-1754d others(7): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484252 | |||||||
chr11:34484308 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0310 a0001c0001t0001g0315 others(1): Show |
4 | HG01106.hp2 HG01175.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-1809G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484308 | |||||||
chr11:34484359 | T | C | 1 | a0001c0001t0002g0248 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.407-1860A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484359 | |||||||
chr11:34484366 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
370 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(367): Show |
intron_variant | MODIFIER | c.407-1867G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484366 | |||||||
chr11:34484379 | C | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.407-1880G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484379 | |||||||
chr11:34484472 | CACTATAC others(2): Show |
C | 35 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0090 others(32): Show |
44 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.407-1982_407-1974d others(11): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484472 | |||||||
chr11:34484472 | CACTATAC others(7): Show |
C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0001g0122 others(10): Show |
16 | HG00544.hp1 HG01106.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.407-1987_407-1974d others(16): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484472 | |||||||
chr11:34484477 | TACTA | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
159 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.407-1982_407-1979d others(6): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484477 | |||||||
chr11:34484481 | A | AACTAT | 21 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0021 others(18): Show |
28 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.407-1987_407-1983d others(7): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | AACTATAC others(3): Show |
6 | a0001c0002t0004g0020 a0001c0002t0004g0027 a0001c0002t0004g0051 others(3): Show |
9 | HG00639.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-1992_407-1983d others(12): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | AT | 13 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0070 others(10): Show |
14 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.407-1983_407-1982i others(3): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | ATACTAT | 8 | a0001c0001t0002g0114 a0001c0001t0007g0214 a0001c0001t0007g0242 others(5): Show |
11 | HG01884.hp2 HG02559.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.407-1983_407-1982i others(8): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | ATACTATC others(4): Show |
9 | a0001c0001t0002g0226 a0001c0001t0002g0312 a0001c0001t0005g0168 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.407-1983_407-1982i others(13): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | ATACTATC others(9): Show |
3 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0007g0258 |
3 | HG01884.hp1 HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.407-1983_407-1982i others(18): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | ATACTATC others(14): Show |
2 | a0001c0001t0005g0256 a0001c0001t0005g0257 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.407-1983_407-1982i others(23): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | ATACTATC others(9): Show |
3 | a0001c0001t0002g0220 a0001c0001t0002g0322 a0001c0001t0014g0210 |
3 | HG02145.hp1 HG02615.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.407-1983_407-1982i others(18): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | ATACTATC others(14): Show |
12 | a0001c0001t0002g0019 a0001c0001t0002g0031 a0001c0001t0002g0073 others(9): Show |
14 | HG00099.hp2 HG01069.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.407-1983_407-1982i others(23): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | ATACTATC others(19): Show |
36 | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0037 others(33): Show |
43 | HG02074.hp1 HG02129.hp2 HG02135.hp1 others(40): Show |
intron_variant | MODIFIER | c.407-1983_407-1982i others(28): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | ATACTATC others(24): Show |
3 | a0001c0001t0002g0048 a0001c0001t0002g0063 a0001c0001t0002g0291 |
3 | HG00609.hp2 HG01496.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.407-1983_407-1982i others(33): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | A | ATACTATC others(24): Show |
1 | a0001c0001t0002g0225 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.407-1983_407-1982i others(33): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | AACTAT | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0015 others(34): Show |
50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.407-1987_407-1983d others(7): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | AACTATAC others(3): Show |
A | 13 | a0001c0001t0003g0002 a0001c0001t0003g0015 a0001c0001t0003g0017 others(10): Show |
14 | HG00735.hp2 HG01981.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.407-1992_407-1983d others(12): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484481 | AACTATAC others(13): Show |
A | 1 | a0001c0001t0003g0133 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.407-2002_407-1983d others(22): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484481 | |||||||
chr11:34484482 | A | C | 32 | a0001c0001t0002g0031 a0001c0001t0002g0073 a0001c0001t0002g0083 others(29): Show |
37 | HG00099.hp2 HG01069.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.407-1983T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484482 | |||||||
chr11:34484487 | A | C | 11 | a0001c0001t0001g0136 a0001c0001t0001g0158 a0001c0001t0001g0188 others(8): Show |
11 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(8): Show |
intron_variant | MODIFIER | c.407-1988T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484487 | |||||||
chr11:34484492 | A | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(41): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.407-1993T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484492 | |||||||
chr11:34484497 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.407-1998T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484497 | |||||||
chr11:34484528 | T | C | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.407-2029A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484528 | |||||||
chr11:34484791 | T | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.407-2292A>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484791 | |||||||
chr11:34484974 | G | T | 3 | a0002c0003t0001g0008 a0002c0003t0001g0012 a0002c0003t0001g0153 |
9 | NA18957.hp1 NA18964.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.407-2475C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34484974 | |||||||
chr11:34485023 | A | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0087 a0001c0001t0003g0115 others(6): Show |
12 | HG00544.hp2 HG02027.hp1 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.407-2524T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485023 | |||||||
chr11:34485058 | C | T | 1 | a0001c0001t0005g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.407-2559G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485058 | |||||||
chr11:34485175 | G | A | 2 | a0001c0001t0005g0232 a0001c0001t0005g0299 |
2 | HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.407-2676C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485175 | |||||||
chr11:34485179 | G | GAA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(77): Show |
105 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.407-2681_407-2680i others(4): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485179 | |||||||
chr11:34485303 | C | A | 3 | a0001c0001t0002g0107 a0001c0001t0002g0179 a0001c0001t0002g0212 |
3 | NA18747.hp1 NA18945.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.407-2804G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485303 | |||||||
chr11:34485450 | C | A | 2 | a0001c0001t0002g0226 a0001c0001t0002g0312 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.407-2951G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485450 | |||||||
chr11:34485624 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.407-3125C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485624 | |||||||
chr11:34485639 | G | A | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.407-3140C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485639 | |||||||
chr11:34485666 | C | T | 55 | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0031 others(52): Show |
66 | HG00099.hp2 HG00609.hp2 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.407-3167G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485666 | |||||||
chr11:34485792 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.407-3293T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485792 | |||||||
chr11:34485860 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(54): Show |
94 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.407-3361G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34485860 | |||||||
chr11:34486000 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.407-3501G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486000 | |||||||
chr11:34486072 | C | T | 1 | a0001c0002t0004g0138 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.407-3573G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486072 | |||||||
chr11:34486109 | G | A | 2 | a0001c0001t0011g0249 a0001c0001t0011g0304 |
2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.407-3610C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486109 | |||||||
chr11:34486332 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(117): Show |
169 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.406+3677C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486332 | |||||||
chr11:34486498 | GC | G | 5 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0297 others(2): Show |
6 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+3510delG | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486498 | |||||||
chr11:34486538 | G | C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0139 |
3 | NA18972.hp1 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.406+3471C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486538 | |||||||
chr11:34486552 | G | C | 1 | a0001c0001t0009g0103 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.406+3457C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486552 | |||||||
chr11:34486581 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(193): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.406+3428A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486581 | |||||||
chr11:34486592 | G | A | 2 | a0001c0001t0005g0168 a0001c0001t0005g0308 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.406+3417C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486592 | |||||||
chr11:34486714 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.406+3295T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486714 | |||||||
chr11:34486785 | C | T | 5 | a0001c0001t0007g0214 a0001c0001t0007g0242 a0001c0001t0007g0258 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+3224G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486785 | |||||||
chr11:34486838 | G | A | 2 | a0001c0001t0005g0168 a0001c0001t0005g0308 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.406+3171C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486838 | |||||||
chr11:34486879 | C | A | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.406+3130G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486879 | |||||||
chr11:34486880 | C | T | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.406+3129G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486880 | |||||||
chr11:34486898 | G | C | 7 | a0001c0001t0007g0130 a0001c0001t0007g0219 a0001c0001t0007g0300 others(4): Show |
10 | HG02572.hp1 HG02615.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.406+3111C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486898 | |||||||
chr11:34486899 | G | A | 1 | a0001c0001t0012g0052 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.406+3110C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34486899 | |||||||
chr11:34487011 | T | C | 1 | a0001c0002t0004g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.406+2998A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487011 | |||||||
chr11:34487070 | C | A | 1 | a0001c0001t0001g0283 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.406+2939G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487070 | |||||||
chr11:34487072 | C | T | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.406+2937G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487072 | |||||||
chr11:34487193 | G | A | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.406+2816C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487193 | |||||||
chr11:34487245 | C | T | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.406+2764G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487245 | |||||||
chr11:34487292 | G | A | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.406+2717C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487292 | |||||||
chr11:34487303 | G | A | 3 | a0001c0001t0003g0148 a0001c0001t0003g0149 a0001c0001t0003g0160 |
3 | HG00544.hp2 NA18975.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.406+2706C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487303 | |||||||
chr11:34487304 | G | C | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.406+2705C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487304 | |||||||
chr11:34487345 | C | T | 1 | a0002c0003t0001g0099 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.406+2664G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487345 | |||||||
chr11:34487504 | A | G | 1 | a0001c0001t0003g0041 | 2 | NA19065.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.406+2505T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487504 | |||||||
chr11:34487554 | C | T | 2 | a0001c0001t0005g0168 a0001c0001t0005g0308 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.406+2455G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487554 | |||||||
chr11:34487653 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.406+2356C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487653 | |||||||
chr11:34487669 | C | T | 1 | a0001c0001t0005g0321 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.406+2340G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487669 | |||||||
chr11:34487704 | C | T | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.406+2305G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487704 | |||||||
chr11:34487753 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.406+2256C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487753 | |||||||
chr11:34487771 | G | A | 1 | a0001c0001t0002g0031 | 3 | HG01069.hp2 HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.406+2238C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487771 | |||||||
chr11:34487829 | A | G | 1 | a0001c0001t0003g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.406+2180T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487829 | |||||||
chr11:34487861 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
82 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.406+2148T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487861 | |||||||
chr11:34487973 | C | T | 2 | a0001c0001t0011g0249 a0001c0001t0011g0304 |
2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.406+2036G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34487973 | |||||||
chr11:34488096 | A | C | 30 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(27): Show |
43 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.406+1913T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488096 | |||||||
chr11:34488237 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.406+1772G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488237 | |||||||
chr11:34488244 | A | T | 36 | a0001c0001t0005g0040 a0001c0002t0004g0006 a0001c0002t0004g0016 others(33): Show |
50 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.406+1765T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488244 | |||||||
chr11:34488336 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.406+1673C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488336 | |||||||
chr11:34488418 | C | T | 59 | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0031 others(56): Show |
70 | HG00099.hp2 HG00609.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.406+1591G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488418 | |||||||
chr11:34488465 | G | A | 36 | a0001c0001t0005g0040 a0001c0002t0004g0006 a0001c0002t0004g0016 others(33): Show |
50 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.406+1544C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488465 | |||||||
chr11:34488581 | T | A | 1 | a0001c0001t0003g0157 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.406+1428A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488581 | |||||||
chr11:34488790 | A | G | 4 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0005g0256 others(1): Show |
4 | HG01884.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+1219T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488790 | |||||||
chr11:34488867 | A | T | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.406+1142T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488867 | |||||||
chr11:34488928 | C | T | 4 | a0001c0001t0003g0029 a0001c0001t0003g0260 a0001c0001t0003g0264 others(1): Show |
6 | HG00099.hp1 HG00280.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+1081G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34488928 | |||||||
chr11:34489007 | A | T | 6 | a0001c0001t0002g0035 a0001c0001t0002g0064 a0001c0001t0002g0098 others(3): Show |
7 | HG00597.hp1 NA18942.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.406+1002T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489007 | |||||||
chr11:34489018 | C | T | 1 | a0001c0001t0011g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.406+991G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489018 | |||||||
chr11:34489019 | G | A | 3 | a0001c0001t0002g0031 a0001c0001t0002g0091 a0001c0001t0002g0294 |
5 | HG00099.hp2 HG01069.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.406+990C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489019 | |||||||
chr11:34489048 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
82 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.406+961A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489048 | |||||||
chr11:34489114 | C | T | 1 | a0001c0001t0003g0264 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.406+895G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489114 | |||||||
chr11:34489115 | G | A | 1 | a0001c0001t0012g0052 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.406+894C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489115 | |||||||
chr11:34489134 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(120): Show |
173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.406+875G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489134 | |||||||
chr11:34489172 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.406+837C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489172 | |||||||
chr11:34489294 | A | G | 1 | a0001c0001t0009g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.406+715T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489294 | |||||||
chr11:34489331 | G | A | 4 | a0001c0001t0003g0015 a0001c0001t0003g0028 a0001c0001t0003g0074 others(1): Show |
8 | HG02630.hp1 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.406+678C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489331 | |||||||
chr11:34489375 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.406+634C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489375 | |||||||
chr11:34489499 | T | C | 4 | a0001c0002t0004g0119 a0001c0002t0004g0261 a0001c0002t0004g0267 others(1): Show |
4 | HG01081.hp2 HG01123.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.406+510A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489499 | |||||||
chr11:34489568 | G | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
82 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.406+441C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489568 | |||||||
chr11:34489663 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.406+346T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489663 | |||||||
chr11:34489994 | C | A | 38 | a0001c0001t0005g0040 a0001c0001t0005g0168 a0001c0001t0005g0308 others(35): Show |
52 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.406+15G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 4/6 | chr11 | 34489994 | |||||||
chr11:34490063 | G | T | 1 | a0001c0001t0003g0233 | 1 | HG02895.hp2 | splice_region_variant&intron_variant | LOW | c.356-4C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490063 | |||||||
chr11:34490301 | G | A | 4 | a0001c0001t0007g0214 a0001c0001t0007g0242 a0001c0001t0007g0259 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-242C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490301 | |||||||
chr11:34490562 | T | C | 52 | a0001c0001t0005g0040 a0001c0001t0005g0168 a0001c0001t0005g0308 others(49): Show |
69 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.356-503A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490562 | |||||||
chr11:34490630 | T | C | 35 | a0001c0002t0004g0006 a0001c0002t0004g0016 a0001c0002t0004g0020 others(32): Show |
48 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.356-571A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490630 | |||||||
chr11:34490729 | G | T | 1 | a0001c0001t0006g0208 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.356-670C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490729 | |||||||
chr11:34490740 | C | T | 1 | a0001c0001t0005g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.356-681G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490740 | |||||||
chr11:34490762 | A | G | 5 | a0001c0001t0002g0081 a0001c0001t0002g0178 a0001c0001t0002g0206 others(2): Show |
5 | NA18939.hp1 NA18956.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-703T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490762 | |||||||
chr11:34490765 | A | G | 1 | a0001c0001t0003g0149 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.356-706T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490765 | |||||||
chr11:34490854 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.356-795G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490854 | |||||||
chr11:34490891 | C | T | 14 | a0001c0001t0007g0130 a0001c0001t0007g0214 a0001c0001t0007g0219 others(11): Show |
17 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.356-832G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34490891 | |||||||
chr11:34491014 | C | T | 2 | a0001c0001t0011g0249 a0001c0001t0011g0304 |
2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.356-955G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491014 | |||||||
chr11:34491015 | C | G | 52 | a0001c0001t0005g0040 a0001c0001t0005g0168 a0001c0001t0005g0308 others(49): Show |
69 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.356-956G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491015 | |||||||
chr11:34491029 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.356-970G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491029 | |||||||
chr11:34491029 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.356-970G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491029 | |||||||
chr11:34491145 | C | G | 1 | a0001c0001t0005g0321 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.356-1086G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491145 | |||||||
chr11:34491204 | G | A | 55 | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0031 others(52): Show |
66 | HG00099.hp2 HG00609.hp2 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.356-1145C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491204 | |||||||
chr11:34491257 | G | A | 2 | a0001c0002t0004g0113 a0001c0002t0004g0277 |
2 | HG01358.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.356-1198C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491257 | |||||||
chr11:34491435 | AC | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
82 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.356-1377delG | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491435 | |||||||
chr11:34491461 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.356-1402T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491461 | |||||||
chr11:34491478 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
82 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.356-1419T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491478 | |||||||
chr11:34491554 | G | A | 2 | a0001c0001t0005g0256 a0001c0001t0005g0257 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.356-1495C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491554 | |||||||
chr11:34491580 | G | GT | 7 | a0001c0001t0001g0167 a0001c0001t0002g0064 a0001c0001t0005g0062 others(4): Show |
7 | HG01884.hp1 HG02738.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-1522dupA | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491580 | |||||||
chr11:34491580 | GT | G | 6 | a0001c0001t0001g0104 a0001c0001t0002g0063 a0001c0001t0002g0137 others(3): Show |
6 | HG03579.hp2 NA18942.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.356-1522delA | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491580 | |||||||
chr11:34491644 | C | T | 1 | a0001c0001t0010g0288 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.356-1585G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491644 | |||||||
chr11:34491883 | T | A | 52 | a0001c0001t0005g0040 a0001c0001t0005g0168 a0001c0001t0005g0308 others(49): Show |
69 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.355+1596A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34491883 | |||||||
chr11:34492013 | G | C | 18 | a0001c0001t0005g0030 a0001c0001t0005g0050 a0001c0001t0005g0053 others(15): Show |
23 | HG00639.hp2 HG01109.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.355+1466C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492013 | |||||||
chr11:34492016 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.355+1463T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492016 | |||||||
chr11:34492024 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(155): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.355+1455T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492024 | |||||||
chr11:34492120 | A | T | 1 | a0001c0001t0003g0148 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.355+1359T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492120 | |||||||
chr11:34492127 | T | C | 1 | a0001c0001t0003g0162 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.355+1352A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492127 | |||||||
chr11:34492385 | G | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(100): Show |
155 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.355+1094C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492385 | |||||||
chr11:34492387 | G | A | 1 | a0001c0002t0004g0021 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.355+1092C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492387 | |||||||
chr11:34492432 | A | T | 1 | a0001c0001t0001g0166 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.355+1047T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492432 | |||||||
chr11:34492514 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.355+965T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492514 | |||||||
chr11:34492679 | T | C | 2 | a0001c0001t0005g0168 a0001c0001t0005g0308 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.355+800A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492679 | |||||||
chr11:34492724 | C | G | 52 | a0001c0001t0005g0040 a0001c0001t0005g0168 a0001c0001t0005g0308 others(49): Show |
69 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.355+755G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492724 | |||||||
chr11:34492790 | C | T | 1 | a0003c0004t0008g0121 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.355+689G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492790 | |||||||
chr11:34492813 | T | C | 1 | a0001c0001t0002g0156 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.355+666A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492813 | |||||||
chr11:34492865 | C | T | 56 | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0031 others(53): Show |
67 | HG00099.hp2 HG00609.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.355+614G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492865 | |||||||
chr11:34492967 | A | C | 1 | a0001c0001t0002g0175 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.355+512T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34492967 | |||||||
chr11:34493214 | G | A | 4 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0005g0256 others(1): Show |
4 | HG01884.hp1 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+265C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34493214 | |||||||
chr11:34493234 | C | T | 1 | a0001c0001t0005g0308 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.355+245G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34493234 | |||||||
chr11:34493242 | C | A | 1 | a0001c0001t0003g0133 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.355+237G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34493242 | |||||||
chr11:34493249 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.355+230A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34493249 | |||||||
chr11:34493293 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.355+186G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34493293 | |||||||
chr11:34493371 | G | A | 2 | a0001c0002t0004g0051 a0001c0002t0016g0263 |
3 | HG00639.hp1 HG01243.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.355+108C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34493371 | |||||||
chr11:34493394 | T | G | 52 | a0001c0001t0005g0040 a0001c0001t0005g0168 a0001c0001t0005g0308 others(49): Show |
69 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.355+85A>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 3/6 | chr11 | 34493394 | |||||||
chr11:34493715 | G | T | 1 | a0001c0001t0002g0206 | 1 | NA18939.hp1 | splice_region_variant&intron_variant | LOW | c.122-3C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34493715 | |||||||
chr11:34494105 | G | A | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.122-393C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34494105 | |||||||
chr11:34494175 | C | T | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.122-463G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34494175 | |||||||
chr11:34494402 | C | G | 1 | a0001c0001t0005g0040 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.122-690G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34494402 | |||||||
chr11:34494410 | C | T | 1 | a0001c0001t0003g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.122-698G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34494410 | |||||||
chr11:34494546 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(76): Show |
104 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.122-834G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34494546 | |||||||
chr11:34494603 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(156): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.122-891A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34494603 | |||||||
chr11:34494703 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(155): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.122-991A>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34494703 | |||||||
chr11:34495079 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(99): Show |
148 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.122-1367C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495079 | |||||||
chr11:34495164 | G | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(41): Show |
79 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.122-1452C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495164 | |||||||
chr11:34495252 | G | T | 1 | a0001c0001t0005g0321 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122-1540C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495252 | |||||||
chr11:34495309 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(125): Show |
182 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.122-1597T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495309 | |||||||
chr11:34495404 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.122-1692G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495404 | |||||||
chr11:34495437 | G | A | 49 | a0001c0001t0001g0266 a0001c0001t0005g0040 a0001c0001t0005g0062 others(46): Show |
66 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.122-1725C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495437 | |||||||
chr11:34495519 | C | G | 7 | a0001c0001t0005g0256 a0001c0001t0005g0257 a0001c0001t0007g0214 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-1807G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495519 | |||||||
chr11:34495662 | C | T | 2 | a0001c0001t0002g0226 a0001c0001t0002g0312 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.122-1950G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495662 | |||||||
chr11:34495803 | T | C | 1 | a0001c0001t0005g0320 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.122-2091A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495803 | |||||||
chr11:34495826 | T | C | 1 | a0001c0001t0005g0168 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.122-2114A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495826 | |||||||
chr11:34495867 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.122-2155G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495867 | |||||||
chr11:34495926 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(45): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.122-2214A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495926 | |||||||
chr11:34495948 | T | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(47): Show |
85 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.122-2236A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34495948 | |||||||
chr11:34496016 | A | ATTTCT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(45): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.122-2305_122-2304i others(7): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496016 | |||||||
chr11:34496050 | C | CCT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(45): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.122-2339_122-2338i others(4): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496050 | |||||||
chr11:34496103 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.122-2391G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496103 | |||||||
chr11:34496139 | G | A | 10 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0007g0130 others(7): Show |
13 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-2427C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496139 | |||||||
chr11:34496223 | G | C | 2 | a0001c0001t0005g0168 a0001c0001t0005g0308 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.122-2511C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496223 | |||||||
chr11:34496230 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(103): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.122-2518A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496230 | |||||||
chr11:34496385 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.122-2673A>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496385 | |||||||
chr11:34496385 | T | TCCAGAGG others(3): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(43): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.122-2674_122-2673i others(12): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496385 | |||||||
chr11:34496423 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
81 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.122-2711A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496423 | |||||||
chr11:34496453 | C | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
81 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.122-2741G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496453 | |||||||
chr11:34496459 | T | G | 2 | a0001c0001t0002g0226 a0001c0001t0002g0312 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.122-2747A>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496459 | |||||||
chr11:34496475 | C | T | 5 | a0001c0001t0005g0040 a0001c0001t0005g0256 a0001c0001t0005g0257 others(2): Show |
6 | HG01891.hp2 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-2763G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496475 | |||||||
chr11:34496477 | A | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(45): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.122-2765T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496477 | |||||||
chr11:34496494 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(55): Show |
96 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.122-2782A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496494 | |||||||
chr11:34496575 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(45): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.122-2863G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496575 | |||||||
chr11:34496686 | T | C | 2 | a0001c0001t0002g0226 a0001c0001t0002g0312 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.122-2974A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496686 | |||||||
chr11:34496766 | G | A | 2 | a0001c0001t0011g0249 a0001c0001t0011g0304 |
2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.122-3054C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496766 | |||||||
chr11:34496997 | A | T | 4 | a0001c0001t0005g0256 a0001c0001t0005g0257 a0001c0001t0007g0214 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-3285T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34496997 | |||||||
chr11:34497035 | A | G | 1 | a0001c0001t0011g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122-3323T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497035 | |||||||
chr11:34497102 | G | A | 1 | a0001c0001t0003g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.122-3390C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497102 | |||||||
chr11:34497163 | A | C | 7 | a0001c0001t0007g0130 a0001c0001t0007g0219 a0001c0001t0007g0300 others(4): Show |
10 | HG02572.hp1 HG02615.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-3451T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497163 | |||||||
chr11:34497311 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.122-3599T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497311 | |||||||
chr11:34497337 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.122-3625G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497337 | |||||||
chr11:34497391 | G | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.122-3679C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497391 | |||||||
chr11:34497393 | C | T | 37 | a0001c0001t0002g0225 a0001c0001t0005g0030 a0001c0001t0005g0049 others(34): Show |
43 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.122-3681G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497393 | |||||||
chr11:34497677 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.122-3965G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497677 | |||||||
chr11:34497787 | A | C | 1 | a0001c0001t0001g0174 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.122-4075T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497787 | |||||||
chr11:34497810 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.122-4098T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34497810 | |||||||
chr11:34498031 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.122-4319T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498031 | |||||||
chr11:34498050 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(84): Show |
115 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.122-4338A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498050 | |||||||
chr11:34498081 | T | C | 1 | a0001c0001t0003g0265 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.122-4369A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498081 | |||||||
chr11:34498104 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.122-4392T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498104 | |||||||
chr11:34498242 | G | A | 7 | a0001c0001t0007g0130 a0001c0001t0007g0219 a0001c0001t0007g0300 others(4): Show |
10 | HG02572.hp1 HG02615.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-4530C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498242 | |||||||
chr11:34498352 | AT | A | 10 | a0001c0001t0002g0322 a0001c0001t0005g0040 a0001c0001t0005g0256 others(7): Show |
11 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.122-4641delA | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498352 | |||||||
chr11:34498352 | ATT | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
82 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.122-4642_122-4641d others(4): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498352 | |||||||
chr11:34498588 | C | T | 3 | a0001c0001t0002g0226 a0001c0001t0002g0312 a0001c0001t0002g0322 |
3 | HG02145.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.122-4876G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498588 | |||||||
chr11:34498615 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.122-4903G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498615 | |||||||
chr11:34498664 | C | T | 5 | a0001c0001t0005g0256 a0001c0001t0005g0257 a0001c0001t0007g0214 others(2): Show |
5 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-4952G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498664 | |||||||
chr11:34498682 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(45): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.122-4970T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498682 | |||||||
chr11:34498885 | A | G | 1 | a0001c0001t0005g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.122-5173T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498885 | |||||||
chr11:34498963 | C | T | 7 | a0001c0001t0007g0130 a0001c0001t0007g0219 a0001c0001t0007g0300 others(4): Show |
10 | HG02572.hp1 HG02615.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-5251G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34498963 | |||||||
chr11:34499092 | C | CA | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(50): Show |
88 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.122-5381dupT | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34499092 | |||||||
chr11:34499252 | G | T | 2 | a0001c0001t0007g0214 a0001c0001t0007g0258 |
2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.122-5540C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34499252 | |||||||
chr11:34499305 | G | A | 55 | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0031 others(52): Show |
66 | HG00099.hp2 HG00609.hp2 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.122-5593C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34499305 | |||||||
chr11:34499319 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.122-5607C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34499319 | |||||||
chr11:34499467 | C | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(74): Show |
102 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.122-5755G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34499467 | |||||||
chr11:34499554 | A | G | 3 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0007g0242 |
3 | HG01884.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.122-5842T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34499554 | |||||||
chr11:34499813 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.121+5816C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34499813 | |||||||
chr11:34499931 | C | G | 5 | a0001c0001t0002g0081 a0001c0001t0002g0178 a0001c0001t0002g0206 others(2): Show |
5 | NA18939.hp1 NA18956.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+5698G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34499931 | |||||||
chr11:34500048 | ATAAGTCA others(5): Show |
A | 2 | a0001c0001t0003g0015 a0001c0001t0003g0074 |
4 | HG02818.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+5569_121+5580d others(14): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500048 | |||||||
chr11:34500102 | C | T | 55 | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0031 others(52): Show |
66 | HG00099.hp2 HG00609.hp2 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.121+5527G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500102 | |||||||
chr11:34500126 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.121+5503C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500126 | |||||||
chr11:34500216 | C | G | 1 | a0001c0001t0005g0320 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.121+5413G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500216 | |||||||
chr11:34500284 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.121+5345C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500284 | |||||||
chr11:34500319 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+5310T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500319 | |||||||
chr11:34500350 | T | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+5279A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500350 | |||||||
chr11:34500370 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+5259C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500370 | |||||||
chr11:34500427 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0034 others(24): Show |
48 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.121+5202G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500427 | |||||||
chr11:34500475 | T | A | 1 | a0001c0001t0019g0147 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.121+5154A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500475 | |||||||
chr11:34500476 | T | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+5153A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500476 | |||||||
chr11:34500481 | C | T | 1 | a0001c0002t0016g0263 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.121+5148G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500481 | |||||||
chr11:34500555 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0131 |
2 | HG02523.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.121+5074C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500555 | |||||||
chr11:34500682 | G | A | 3 | a0001c0001t0002g0226 a0001c0001t0002g0312 a0001c0001t0002g0322 |
3 | HG02145.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.121+4947C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500682 | |||||||
chr11:34500868 | CT | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.121+4760delA | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500868 | |||||||
chr11:34500968 | TTATCATG others(1): Show |
T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+4653_121+4660d others(10): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34500968 | |||||||
chr11:34501044 | T | A | 5 | a0001c0001t0005g0256 a0001c0001t0005g0257 a0001c0001t0007g0214 others(2): Show |
5 | HG01891.hp2 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+4585A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501044 | |||||||
chr11:34501066 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+4563C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501066 | |||||||
chr11:34501095 | C | T | 3 | a0001c0001t0002g0226 a0001c0001t0002g0312 a0001c0001t0002g0322 |
3 | HG02145.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.121+4534G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501095 | |||||||
chr11:34501134 | G | A | 2 | a0001c0001t0003g0134 a0001c0001t0003g0151 |
2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.121+4495C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501134 | |||||||
chr11:34501318 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(47): Show |
86 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.121+4311T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501318 | |||||||
chr11:34501490 | T | A | 2 | a0001c0001t0005g0241 a0001c0001t0005g0296 |
2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.121+4139A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501490 | |||||||
chr11:34501503 | G | A | 30 | a0001c0001t0001g0126 a0001c0002t0004g0006 a0001c0002t0004g0016 others(27): Show |
43 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.121+4126C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501503 | |||||||
chr11:34501578 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.121+4051G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501578 | |||||||
chr11:34501596 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+4033G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501596 | |||||||
chr11:34501610 | T | C | 1 | a0001c0001t0005g0056 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.121+4019A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501610 | |||||||
chr11:34501626 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+4003C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501626 | |||||||
chr11:34501855 | G | T | 7 | a0001c0001t0007g0130 a0001c0001t0007g0219 a0001c0001t0007g0300 others(4): Show |
10 | HG02572.hp1 HG02615.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.121+3774C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501855 | |||||||
chr11:34501903 | C | T | 2 | a0001c0001t0005g0256 a0001c0001t0005g0257 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.121+3726G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501903 | |||||||
chr11:34501959 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+3670G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34501959 | |||||||
chr11:34502117 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+3512G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502117 | |||||||
chr11:34502177 | G | A | 1 | a0001c0001t0005g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.121+3452C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502177 | |||||||
chr11:34502378 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.121+3251C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502378 | |||||||
chr11:34502421 | C | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(47): Show |
86 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.121+3208G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502421 | |||||||
chr11:34502480 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.121+3149G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502480 | |||||||
chr11:34502481 | G | A | 1 | a0001c0001t0002g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.121+3148C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502481 | |||||||
chr11:34502516 | T | C | 3 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0007g0242 |
3 | HG01884.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.121+3113A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502516 | |||||||
chr11:34502575 | C | G | 2 | a0001c0001t0005g0040 a0001c0001t0011g0249 |
3 | HG02896.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.121+3054G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502575 | |||||||
chr11:34502614 | C | T | 1 | a0001c0001t0005g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.121+3015G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502614 | |||||||
chr11:34502664 | C | T | 1 | a0001c0001t0019g0147 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.121+2965G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502664 | |||||||
chr11:34502671 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+2958G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502671 | |||||||
chr11:34502737 | G | T | 3 | a0001c0001t0002g0226 a0001c0001t0002g0312 a0001c0001t0002g0322 |
3 | HG02145.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.121+2892C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502737 | |||||||
chr11:34502874 | C | A | 1 | a0001c0001t0002g0091 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.121+2755G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502874 | |||||||
chr11:34502909 | G | A | 1 | a0001c0001t0005g0321 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.121+2720C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34502909 | |||||||
chr11:34503101 | T | C | 1 | a0001c0001t0002g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.121+2528A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503101 | |||||||
chr11:34503167 | C | CT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+2461dupA | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503167 | |||||||
chr11:34503305 | C | T | 1 | a0001c0001t0011g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.121+2324G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503305 | |||||||
chr11:34503349 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.121+2280C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503349 | |||||||
chr11:34503379 | T | C | 1 | a0001c0001t0006g0077 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.121+2250A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503379 | |||||||
chr11:34503380 | A | G | 1 | a0001c0001t0006g0077 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.121+2249T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503380 | |||||||
chr11:34503451 | T | C | 2 | a0001c0001t0002g0226 a0001c0001t0002g0312 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.121+2178A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503451 | |||||||
chr11:34503456 | G | A | 37 | a0001c0001t0001g0126 a0001c0001t0001g0266 a0001c0002t0004g0006 others(34): Show |
50 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.121+2173C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503456 | |||||||
chr11:34503466 | C | CT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+2162dupA | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503466 | |||||||
chr11:34503542 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(42): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.121+2087C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503542 | |||||||
chr11:34503789 | A | G | 31 | a0001c0001t0001g0126 a0001c0002t0004g0006 a0001c0002t0004g0016 others(28): Show |
44 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.121+1840T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34503789 | |||||||
chr11:34504000 | C | T | 1 | a0001c0001t0003g0087 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.121+1629G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504000 | |||||||
chr11:34504192 | C | T | 21 | a0001c0001t0003g0028 a0001c0001t0003g0233 a0001c0001t0005g0049 others(18): Show |
24 | HG01243.hp2 HG02145.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.121+1437G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504192 | |||||||
chr11:34504225 | G | T | 2 | a0001c0001t0005g0168 a0001c0001t0005g0308 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.121+1404C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504225 | |||||||
chr11:34504265 | G | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0038 others(11): Show |
26 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+1364C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504265 | |||||||
chr11:34504297 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
5 | NA18747.hp2 NA18993.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+1332A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504297 | |||||||
chr11:34504377 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0191 |
4 | HG01255.hp2 HG01346.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+1252C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504377 | |||||||
chr11:34504400 | C | CAT | 2 | a0001c0001t0005g0050 a0001c0001t0005g0251 |
3 | HG01109.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.121+1228_121+1229i others(4): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504400 | |||||||
chr11:34504400 | C | CGT | 44 | a0001c0001t0002g0225 a0001c0001t0003g0015 a0001c0001t0003g0028 others(41): Show |
53 | HG00639.hp2 HG01243.hp2 HG01433.hp2 others(50): Show |
intron_variant | MODIFIER | c.121+1227_121+1228d others(4): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504400 | |||||||
chr11:34504438 | T | C | 2 | a0001c0001t0005g0040 a0001c0001t0011g0249 |
3 | HG02896.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.121+1191A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504438 | |||||||
chr11:34504837 | T | TA | 3 | a0001c0001t0002g0226 a0001c0001t0002g0312 a0001c0001t0002g0322 |
3 | HG02145.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.121+791_121+792ins others(1): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504837 | |||||||
chr11:34504838 | G | A | 3 | a0001c0001t0002g0226 a0001c0001t0002g0312 a0001c0001t0002g0322 |
3 | HG02145.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.121+791C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34504838 | |||||||
chr11:34505312 | C | T | 1 | a0001c0001t0002g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.121+317G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34505312 | |||||||
chr11:34505364 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.121+265C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34505364 | |||||||
chr11:34505484 | C | G | 2 | a0001c0001t0002g0226 a0001c0001t0002g0312 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.121+145G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34505484 | |||||||
chr11:34505549 | T | A | 2 | a0001c0001t0002g0226 a0001c0001t0002g0312 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.121+80A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34505549 | |||||||
chr11:34505605 | A | G | 30 | a0001c0001t0001g0126 a0001c0002t0004g0006 a0001c0002t0004g0016 others(27): Show |
43 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.121+24T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 2/6 | chr11 | 34505605 | |||||||
chr11:34505833 | C | T | 1 | a0001c0001t0011g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-4-80G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34505833 | |||||||
chr11:34505846 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-4-93A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34505846 | |||||||
chr11:34505889 | G | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(51): Show |
91 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.-4-136C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34505889 | |||||||
chr11:34506005 | G | A | 1 | a0001c0002t0004g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-4-252C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506005 | |||||||
chr11:34506042 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-4-289C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506042 | |||||||
chr11:34506090 | T | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(40): Show |
78 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.-4-337A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506090 | |||||||
chr11:34506302 | A | G | 36 | a0001c0001t0001g0126 a0001c0001t0001g0266 a0001c0002t0004g0006 others(33): Show |
49 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.-4-549T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506302 | |||||||
chr11:34506348 | G | A | 3 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0007g0242 |
3 | HG01884.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-4-595C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506348 | |||||||
chr11:34506354 | G | A | 36 | a0001c0001t0001g0126 a0001c0001t0001g0266 a0001c0002t0004g0006 others(33): Show |
49 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.-4-601C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506354 | |||||||
chr11:34506427 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-4-674T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506427 | |||||||
chr11:34506455 | A | G | 50 | a0001c0001t0002g0225 a0001c0001t0003g0015 a0001c0001t0003g0028 others(47): Show |
61 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4-702T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506455 | |||||||
chr11:34506617 | G | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-4-864C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506617 | |||||||
chr11:34506638 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-4-885G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506638 | |||||||
chr11:34506814 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-4-1061C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506814 | |||||||
chr11:34506819 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-4-1066T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506819 | |||||||
chr11:34506999 | A | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(39): Show |
77 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.-4-1246T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34506999 | |||||||
chr11:34507092 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4-1339A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507092 | |||||||
chr11:34507155 | C | T | 1 | a0001c0002t0004g0111 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-4-1402G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507155 | |||||||
chr11:34507171 | A | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-4-1418T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507171 | |||||||
chr11:34507219 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
178 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-4-1466G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507219 | |||||||
chr11:34507271 | T | C | 3 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0007g0242 |
3 | HG01884.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-4-1518A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507271 | |||||||
chr11:34507421 | G | A | 2 | a0001c0001t0005g0040 a0001c0001t0011g0249 |
3 | HG02896.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-4-1668C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507421 | |||||||
chr11:34507551 | G | T | 1 | a0001c0001t0002g0035 | 2 | NA18995.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-4-1798C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507551 | |||||||
chr11:34507631 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(43): Show |
82 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.-4-1878C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507631 | |||||||
chr11:34507651 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-4-1898T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507651 | |||||||
chr11:34507762 | A | G | 3 | a0001c0001t0005g0062 a0001c0001t0005g0186 a0001c0001t0007g0242 |
3 | HG01884.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-4-2009T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507762 | |||||||
chr11:34507919 | G | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
83 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-4-2166C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34507919 | |||||||
chr11:34508228 | G | A | 1 | a0001c0001t0011g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-4-2475C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508228 | |||||||
chr11:34508267 | C | T | 2 | a0001c0001t0005g0256 a0001c0001t0005g0257 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-4-2514G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508267 | |||||||
chr11:34508284 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(183): Show |
256 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-4-2531A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508284 | |||||||
chr11:34508395 | C | T | 1 | a0001c0001t0005g0320 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-4-2642G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508395 | |||||||
chr11:34508422 | G | C | 3 | a0001c0001t0005g0106 a0001c0001t0005g0237 a0001c0001t0005g0311 |
3 | HG02622.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-4-2669C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508422 | |||||||
chr11:34508444 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0158 |
2 | HG00408.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.-4-2691T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508444 | |||||||
chr11:34508469 | C | T | 1 | a0001c0001t0010g0301 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-4-2716G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508469 | |||||||
chr11:34508481 | C | T | 2 | a0001c0001t0002g0226 a0001c0001t0002g0312 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-4-2728G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508481 | |||||||
chr11:34508505 | AAAAAAAT others(7): Show |
A | 1 | a0001c0001t0001g0253 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-4-2766_-4-2753del others(14): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508505 | |||||||
chr11:34508519 | T | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
97 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-4-2766A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508519 | |||||||
chr11:34508571 | G | T | 1 | a0001c0001t0003g0086 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-4-2818C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508571 | |||||||
chr11:34508721 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0001g0122 others(9): Show |
15 | HG02040.hp2 NA18949.hp2 NA18970.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4-2968A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508721 | |||||||
chr11:34508724 | T | C | 54 | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0031 others(51): Show |
65 | HG00099.hp2 HG00609.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.-4-2971A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34508724 | |||||||
chr11:34509051 | C | T | 17 | a0001c0001t0002g0225 a0001c0001t0003g0015 a0001c0001t0003g0074 others(14): Show |
23 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-3298G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509051 | |||||||
chr11:34509057 | C | T | 1 | a0001c0002t0004g0111 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-4-3304G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509057 | |||||||
chr11:34509212 | C | T | 4 | a0001c0001t0005g0186 a0001c0001t0005g0308 a0001c0001t0005g0321 others(1): Show |
4 | HG01884.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-3459G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509212 | |||||||
chr11:34509213 | C | T | 2 | a0001c0001t0002g0322 a0001c0001t0007g0219 |
2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-4-3460G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509213 | |||||||
chr11:34509328 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(225): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-4-3575C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509328 | |||||||
chr11:34509335 | A | G | 1 | a0001c0002t0004g0138 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-4-3582T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509335 | |||||||
chr11:34509354 | C | T | 3 | a0001c0001t0002g0291 a0001c0001t0002g0312 a0001c0001t0008g0011 |
6 | HG01496.hp2 HG02809.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-3601G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509354 | |||||||
chr11:34509470 | T | C | 14 | a0001c0001t0002g0181 a0001c0001t0002g0322 a0001c0001t0005g0030 others(11): Show |
18 | HG00735.hp1 HG01109.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-4-3717A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509470 | |||||||
chr11:34509586 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0005g0311 a0001c0002t0016g0263 |
3 | HG01099.hp1 HG01358.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-4-3833T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509586 | |||||||
chr11:34509615 | A | T | 129 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0057 others(126): Show |
157 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-4-3862T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509615 | |||||||
chr11:34509630 | G | A | 1 | a0001c0001t0007g0242 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-4-3877C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509630 | |||||||
chr11:34509743 | G | A | 21 | a0001c0001t0001g0274 a0001c0001t0001g0285 a0001c0001t0001g0287 others(18): Show |
22 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.-5+3934C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509743 | |||||||
chr11:34509863 | C | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.-5+3814G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509863 | |||||||
chr11:34509894 | T | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
9 | HG02074.hp1 NA18970.hp1 NA19010.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+3783A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34509894 | |||||||
chr11:34510117 | T | C | 1 | a0001c0001t0003g0217 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-5+3560A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510117 | |||||||
chr11:34510118 | A | T | 1 | a0001c0001t0003g0217 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-5+3559T>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510118 | |||||||
chr11:34510294 | TA | T | 4 | a0001c0001t0005g0256 a0001c0001t0005g0257 a0001c0001t0007g0258 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+3382delT | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510294 | |||||||
chr11:34510311 | G | GT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(79): Show |
116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-5+3365dupA | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510311 | |||||||
chr11:34510311 | G | GTT | 26 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0136 others(23): Show |
29 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-5+3364_-5+3365dup others(2): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510311 | |||||||
chr11:34510378 | C | G | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0274 others(18): Show |
29 | HG00323.hp2 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-5+3299G>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510378 | |||||||
chr11:34510627 | G | A | 4 | a0001c0001t0005g0256 a0001c0001t0005g0257 a0001c0001t0007g0258 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+3050C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510627 | |||||||
chr11:34510657 | T | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0274 others(18): Show |
29 | HG00323.hp2 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-5+3020A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510657 | |||||||
chr11:34510820 | G | C | 2 | a0001c0001t0001g0270 a0001c0002t0004g0269 |
2 | HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-5+2857C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510820 | |||||||
chr11:34510920 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-5+2757G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510920 | |||||||
chr11:34510936 | T | G | 1 | a0001c0001t0006g0215 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-5+2741A>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510936 | |||||||
chr11:34510947 | A | G | 42 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0266 others(39): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.-5+2730T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510947 | |||||||
chr11:34510989 | T | C | 27 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(24): Show |
30 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5+2688A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34510989 | |||||||
chr11:34511022 | T | C | 1 | a0001c0002t0004g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-5+2655A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511022 | |||||||
chr11:34511403 | C | T | 4 | a0001c0001t0005g0256 a0001c0001t0005g0257 a0001c0001t0007g0258 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+2274G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511403 | |||||||
chr11:34511410 | G | T | 1 | a0001c0001t0007g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-5+2267C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511410 | |||||||
chr11:34511446 | T | C | 16 | a0001c0001t0001g0266 a0001c0001t0001g0270 a0001c0001t0001g0271 others(13): Show |
20 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-5+2231A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511446 | |||||||
chr11:34511455 | A | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0274 others(20): Show |
31 | HG00323.hp2 HG00639.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+2222T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511455 | |||||||
chr11:34511497 | GAATCAGG others(15): Show |
G | 1 | a0001c0002t0004g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-5+2158_-5+2179del others(22): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511497 | |||||||
chr11:34511683 | C | A | 1 | a0001c0001t0002g0216 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-5+1994G>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511683 | |||||||
chr11:34511778 | G | A | 28 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(25): Show |
31 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.-5+1899C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511778 | |||||||
chr11:34511801 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-5+1876A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511801 | |||||||
chr11:34511984 | T | A | 1 | a0001c0001t0003g0273 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-5+1693A>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34511984 | |||||||
chr11:34512033 | G | A | 5 | a0001c0001t0002g0244 a0001c0001t0002g0246 a0001c0001t0002g0247 others(2): Show |
5 | NA18959.hp2 NA18971.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1644C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512033 | |||||||
chr11:34512050 | G | T | 2 | a0001c0001t0001g0307 a0001c0001t0005g0308 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-5+1627C>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512050 | |||||||
chr11:34512257 | TTGC | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(187): Show |
250 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.-5+1417_-5+1419del others(3): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512257 | |||||||
chr11:34512314 | C | T | 16 | a0001c0001t0001g0310 a0001c0001t0001g0315 a0001c0001t0001g0318 others(13): Show |
18 | HG00738.hp2 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-5+1363G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512314 | |||||||
chr11:34512317 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-5+1360C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512317 | |||||||
chr11:34512488 | A | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(192): Show |
255 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.-5+1189T>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512488 | |||||||
chr11:34512543 | C | T | 1 | a0001c0001t0003g0127 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-5+1134G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512543 | |||||||
chr11:34512583 | A | AT | 9 | a0001c0001t0001g0253 a0001c0001t0002g0252 a0001c0001t0005g0050 others(6): Show |
10 | HG01109.hp2 HG01515.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5+1093dupA | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512583 | |||||||
chr11:34512583 | A | ATT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(178): Show |
240 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.-5+1092_-5+1093dup others(2): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512583 | |||||||
chr11:34512583 | AT | A | 19 | a0001c0001t0001g0266 a0001c0001t0001g0270 a0001c0001t0001g0271 others(16): Show |
23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+1093delA | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512583 | |||||||
chr11:34512583 | ATT | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0274 others(20): Show |
31 | HG00323.hp2 HG00639.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.-5+1092_-5+1093del others(2): Show |
ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512583 | |||||||
chr11:34512626 | C | T | 1 | a0001c0002t0004g0060 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-5+1051G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512626 | |||||||
chr11:34512747 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-5+930C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512747 | |||||||
chr11:34512794 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-5+883C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512794 | |||||||
chr11:34512999 | T | C | 2 | a0001c0001t0001g0307 a0001c0001t0005g0308 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-5+678A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34512999 | |||||||
chr11:34513110 | G | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(234): Show |
309 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-5+567C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34513110 | |||||||
chr11:34513341 | A | G | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02074.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-5+336T>C | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34513341 | |||||||
chr11:34513355 | T | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0274 others(34): Show |
47 | HG00323.hp2 HG00639.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.-5+322A>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34513355 | |||||||
chr11:34513514 | G | C | 1 | a0001c0001t0001g0323 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-5+163C>G | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34513514 | |||||||
chr11:34513584 | G | A | 37 | a0001c0001t0001g0293 a0001c0001t0001g0297 a0001c0001t0001g0298 others(34): Show |
43 | HG00738.hp2 HG01069.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.-5+93C>T | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34513584 | |||||||
chr11:34513615 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-5+62G>A | ELF5 | ENSG00000135374.11 | transcript | ENST00000257832.7 | protein_coding | 1/6 | chr11 | 34513615 |