Item | Value |
---|---|
geneid | 26298 |
ensemblid | ENSG00000135373.13 |
hgncid | 3246 |
symbol | EHF |
name | ETS homologous factor |
refseq_nuc | NM_012153.6 |
refseq_prot | NP_036285.2 |
ensembl_nuc | ENST00000257831.8 |
ensembl_prot | ENSP00000257831.3 |
mane_status | MANE Select |
chr | chr11 |
start | 34621093 |
end | 34663288 |
strand | + |
ver | v1.2 |
region | chr11:34621093-34663288 |
region5000 | chr11:34616093-34668288 |
regionname0 | EHF_chr11_34621093_34663288 |
regionname5000 | EHF_chr11_34616093_34668288 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 300 | 399 | 92 | 74 | 177 | 12 | 42 | 141 | EHF_chr11_34616093_34668288 | EHF | MILEG others(295): Show |
chr11 | 34616093 | 34668288 |
a0002 | 0/0 | 300 | 10 | 0 | 2 | 6 | 0 | 2 | 5 | EHF_chr11_34616093_34668288 | EHF | MILEG others(295): Show |
chr11 | 34616093 | 34668288 |
a0003 | 0/0 | 300 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | MILEG others(295): Show |
chr11 | 34616093 | 34668288 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 900 | 259 | 69 | 52 | 107 | 8 | 22 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 | ||
a0001c0002 | 0/0 | 900 | 91 | 10 | 16 | 55 | 1 | 9 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 | ||
a0001c0003 | 0/1 | 900 | 30 | 7 | 5 | 3 | 3 | 11 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 | ||
a0001c0004 | 0/0 | 900 | 11 | 0 | 1 | 10 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 | ||
a0001c0006 | 0/0 | 900 | 6 | 6 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 | ||
a0001c0007 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 | ||
a0001c0010 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 | ||
a0002c0005 | 0/0 | 900 | 9 | 0 | 2 | 6 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 | ||
a0002c0009 | 0/0 | 900 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 | ||
a0003c0008 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ATGAT others(895): Show |
chr11 | 34616093 | 34668288 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5399 | 51 | 2 | 21 | 25 | 1 | 2 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0002 | 0/0 | 5399 | 47 | 3 | 16 | 16 | 2 | 10 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0003 | 0/0 | 5399 | 35 | 0 | 3 | 32 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0004 | 0/0 | 5399 | 2 | 1 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0005 | 0/0 | 5399 | 4 | 0 | 4 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0006 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0007 | 0/0 | 5399 | 18 | 1 | 3 | 11 | 0 | 3 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0008 | 0/0 | 5399 | 4 | 0 | 1 | 2 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0009 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0010 | 0/0 | 5399 | 13 | 1 | 0 | 10 | 0 | 2 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0012 | 0/0 | 5399 | 6 | 6 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0013 | 0/0 | 5399 | 4 | 4 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0014 | 0/0 | 5399 | 7 | 6 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0015 | 0/0 | 5399 | 5 | 0 | 0 | 1 | 1 | 3 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0016 | 0/0 | 5399 | 3 | 2 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0017 | 0/0 | 5399 | 5 | 4 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0019 | 0/0 | 5399 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0021 | 0/0 | 5399 | 3 | 3 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0022 | 0/0 | 5399 | 3 | 3 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0026 | 0/0 | 5399 | 2 | 0 | 0 | 2 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0027 | 0/0 | 5399 | 2 | 0 | 0 | 0 | 0 | 2 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0028 | 0/0 | 5399 | 2 | 0 | 0 | 0 | 2 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0029 | 0/0 | 5399 | 2 | 0 | 0 | 2 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0031 | 0/0 | 5399 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0032 | 0/0 | 5399 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0033 | 0/0 | 5399 | 2 | 1 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0035 | 0/0 | 5399 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0036 | 0/0 | 5399 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0038 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0041 | 1/0 | 5399 | 1 | 0 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0042 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0045 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0046 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0047 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0050 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0053 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0054 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0055 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0057 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0060 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0061 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0062 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0063 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0064 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0065 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0066 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0067 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0068 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0069 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0072 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0074 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0075 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0079 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0080 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0001t0081 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0001 | 0/0 | 5399 | 2 | 0 | 1 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0002 | 0/0 | 5399 | 3 | 1 | 0 | 0 | 1 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0004 | 0/0 | 5399 | 24 | 0 | 8 | 13 | 0 | 3 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0006 | 0/0 | 5399 | 17 | 0 | 0 | 17 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0008 | 0/0 | 5399 | 13 | 0 | 1 | 10 | 0 | 2 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0009 | 0/0 | 5399 | 12 | 0 | 0 | 11 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0012 | 0/0 | 5399 | 3 | 3 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0016 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0019 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0023 | 0/0 | 5399 | 3 | 0 | 3 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0024 | 0/0 | 5399 | 2 | 1 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0025 | 0/0 | 5399 | 2 | 0 | 0 | 2 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0034 | 0/0 | 5399 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0039 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0043 | 0/0 | 5399 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0044 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0048 | 0/0 | 5399 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0071 | 0/0 | 5399 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0002t0073 | 0/0 | 5399 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0005 | 0/0 | 5399 | 12 | 5 | 1 | 0 | 0 | 6 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0011 | 0/0 | 5399 | 3 | 1 | 0 | 1 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0016 | 0/0 | 5399 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0018 | 0/0 | 5399 | 5 | 0 | 2 | 0 | 3 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0020 | 0/0 | 5399 | 2 | 0 | 0 | 1 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0030 | 0/0 | 5399 | 2 | 0 | 1 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0040 | 0/0 | 5399 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0051 | 0/0 | 5382 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5377): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0058 | 0/1 | 5399 | 1 | 0 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0077 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0003t0078 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0004t0005 | 0/0 | 5399 | 4 | 0 | 0 | 4 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0004t0011 | 0/0 | 5399 | 5 | 0 | 0 | 5 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0004t0049 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0004t0052 | 0/0 | 5399 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0006t0013 | 0/0 | 5399 | 3 | 3 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0006t0037 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0006t0056 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0006t0059 | 0/0 | 5399 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0007t0070 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0001c0010t0001 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0002c0005t0005 | 0/0 | 5399 | 4 | 0 | 0 | 3 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0002c0005t0006 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0002c0005t0009 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0002c0005t0011 | 0/0 | 5399 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0002c0005t0020 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0002c0005t0076 | 0/0 | 5399 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0002c0009t0015 | 0/0 | 5399 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
a0003c0008t0003 | 0/0 | 5399 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | ACTCT others(5394): Show |
chr11 | 34616093 | 34668288 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0001 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0004g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0005g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0007g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0008g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0008g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0010g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0012g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0012g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0012g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0012g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0012g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0013g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0013g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0013g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0013g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0014g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0014g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0014g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0014g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0014g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0015g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0015g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0015g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0015g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0015g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0016g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0016g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0016g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0017g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0017g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0017g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0017g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0019g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0019g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0021g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0021g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0021g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0022g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0022g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0022g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0026g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0027g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0027g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0028g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0028g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0029g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0029g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0031g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0031g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0032g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0032g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0033g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0033g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0035g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0036g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0036g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0038g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0041g0347 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0042g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0045g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0046g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0047g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0050g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0053g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0054g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0055g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0057g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0060g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0061g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0062g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0063g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0064g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0065g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0066g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0067g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0068g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0069g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0072g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0074g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0075g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0079g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0080g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0001t0081g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0008g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0009g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0012g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0012g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0019g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0023g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0023g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0023g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0024g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0024g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0025g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0025g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0034g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0034g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0039g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0043g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0044g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0048g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0071g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0002t0073g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0005g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0011g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0016g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0018g0005 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0018g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0018g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0020g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0020g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0030g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0030g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0040g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0051g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0058g0330 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0077g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0003t0078g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0011g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0011g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0011g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0011g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0011g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0049g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0004t0052g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0006t0013g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0006t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0006t0013g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0006t0037g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0006t0056g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0006t0059g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0007t0070g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0001c0010t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0002c0005t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0002c0005t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0002c0005t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0002c0005t0006g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0002c0005t0009g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0002c0005t0011g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0002c0005t0020g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0002c0005t0076g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0002c0009t0015g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
a0003c0008t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0033 | g0252 | EUR | GBR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0138 | EUR | GBR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | FIN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0212 | EUR | FIN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00408 | hp1 | a0001 | c0002 | t0006 | g0276 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00408 | hp2 | a0001 | c0001 | t0010 | g0360 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00423 | hp1 | a0001 | c0001 | t0007 | g0049 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00423 | hp2 | a0002 | c0005 | t0020 | g0349 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00597 | hp1 | a0001 | c0001 | t0008 | g0073 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00621 | hp2 | a0001 | c0002 | t0004 | g0136 | EAS | CHS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0123 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00733 | hp2 | a0001 | c0004 | t0052 | g0032 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00735 | hp1 | a0002 | c0005 | t0076 | g0145 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00738 | hp2 | a0001 | c0003 | t0005 | g0141 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0067 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG00741 | hp2 | a0001 | c0002 | t0004 | g0213 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0191 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01074 | hp1 | a0001 | c0002 | t0023 | g0135 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01074 | hp2 | a0001 | c0003 | t0030 | g0100 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0332 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01099 | hp2 | a0001 | c0002 | t0004 | g0142 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01109 | hp2 | a0001 | c0001 | t0016 | g0255 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01167 | hp2 | a0001 | c0003 | t0018 | g0005 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01168 | hp1 | a0001 | c0002 | t0073 | g0282 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01169 | hp2 | a0001 | c0003 | t0018 | g0171 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01175 | hp2 | a0001 | c0002 | t0004 | g0134 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01243 | hp1 | a0001 | c0001 | t0014 | g0371 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01257 | hp2 | a0001 | c0002 | t0004 | g0012 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01258 | hp2 | a0001 | c0002 | t0004 | g0012 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01261 | hp1 | a0001 | c0002 | t0004 | g0211 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01346 | hp1 | a0001 | c0003 | t0051 | g0318 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01358 | hp1 | a0001 | c0002 | t0071 | g0116 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01361 | hp1 | a0001 | c0002 | t0004 | g0163 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01361 | hp2 | a0001 | c0001 | t0007 | g0097 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01496 | hp1 | a0001 | c0001 | t0017 | g0373 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01515 | hp1 | a0001 | c0001 | t0015 | g0352 | EUR | IBS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01515 | hp2 | a0001 | c0001 | t0028 | g0316 | EUR | IBS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01516 | hp1 | a0001 | c0003 | t0018 | g0005 | EUR | IBS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01517 | hp1 | a0001 | c0001 | t0028 | g0327 | EUR | IBS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01517 | hp2 | a0001 | c0003 | t0018 | g0005 | EUR | IBS | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0378 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01884 | hp2 | a0001 | c0001 | t0013 | g0309 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01891 | hp1 | a0001 | c0001 | t0014 | g0218 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01891 | hp2 | a0001 | c0003 | t0005 | g0190 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01952 | hp2 | a0001 | c0002 | t0023 | g0130 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01975 | hp1 | a0001 | c0002 | t0048 | g0329 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01978 | hp1 | a0002 | c0005 | t0011 | g0311 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01993 | hp1 | a0001 | c0002 | t0008 | g0321 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02015 | hp1 | a0001 | c0001 | t0015 | g0353 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02027 | hp1 | a0001 | c0001 | t0007 | g0066 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02027 | hp2 | a0001 | c0002 | t0006 | g0231 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02040 | hp1 | a0001 | c0001 | t0010 | g0344 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02040 | hp2 | a0001 | c0003 | t0020 | g0343 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0098 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02055 | hp2 | a0001 | c0002 | t0039 | g0345 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02056 | hp1 | a0001 | c0004 | t0049 | g0086 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02083 | hp2 | a0001 | c0001 | t0069 | g0277 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02129 | hp2 | a0001 | c0002 | t0006 | g0292 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02132 | hp2 | a0001 | c0002 | t0006 | g0258 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02135 | hp1 | a0001 | c0002 | t0008 | g0052 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02135 | hp2 | a0001 | c0004 | t0005 | g0259 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02145 | hp1 | a0001 | c0001 | t0032 | g0176 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02145 | hp2 | a0001 | c0001 | t0066 | g0197 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02148 | hp1 | a0001 | c0002 | t0004 | g0154 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02155 | hp1 | a0003 | c0008 | t0003 | g0059 | EAS | CDX | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02155 | hp2 | a0001 | c0001 | t0010 | g0342 | EAS | CDX | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | CDX | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02257 | hp1 | a0001 | c0002 | t0034 | g0230 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02257 | hp2 | a0001 | c0001 | t0012 | g0021 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02258 | hp1 | a0001 | c0001 | t0022 | g0102 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0319 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02273 | hp2 | a0001 | c0002 | t0023 | g0257 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02280 | hp1 | a0001 | c0001 | t0045 | g0181 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02280 | hp2 | a0001 | c0006 | t0059 | g0199 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0320 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02523 | hp1 | a0001 | c0001 | t0010 | g0354 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02523 | hp2 | a0001 | c0002 | t0008 | g0058 | EAS | KHV | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02572 | hp1 | a0001 | c0002 | t0016 | g0182 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02572 | hp2 | a0001 | c0001 | t0013 | g0324 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02615 | hp1 | a0001 | c0001 | t0017 | g0017 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02615 | hp2 | a0001 | c0001 | t0016 | g0379 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02622 | hp1 | a0001 | c0001 | t0057 | g0178 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02622 | hp2 | a0001 | c0003 | t0005 | g0014 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02630 | hp1 | a0001 | c0001 | t0019 | g0341 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02630 | hp2 | a0001 | c0003 | t0005 | g0014 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02647 | hp1 | a0001 | c0006 | t0037 | g0355 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02647 | hp2 | a0001 | c0001 | t0054 | g0308 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02698 | hp1 | a0002 | c0005 | t0005 | g0242 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02698 | hp2 | a0001 | c0002 | t0004 | g0151 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02717 | hp1 | a0001 | c0001 | t0047 | g0101 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02717 | hp2 | a0001 | c0003 | t0078 | g0186 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02723 | hp1 | a0001 | c0001 | t0080 | g0298 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02723 | hp2 | a0001 | c0001 | t0031 | g0179 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02735 | hp1 | a0001 | c0003 | t0005 | g0271 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02738 | hp2 | a0001 | c0002 | t0004 | g0214 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02809 | hp1 | a0001 | c0001 | t0079 | g0228 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02809 | hp2 | a0001 | c0001 | t0031 | g0312 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02818 | hp2 | a0001 | c0002 | t0012 | g0170 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02886 | hp1 | a0001 | c0001 | t0053 | g0177 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02895 | hp1 | a0001 | c0001 | t0021 | g0103 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02895 | hp2 | a0001 | c0001 | t0067 | g0376 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02896 | hp1 | a0001 | c0006 | t0013 | g0111 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02896 | hp2 | a0001 | c0003 | t0005 | g0174 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02897 | hp1 | a0001 | c0001 | t0021 | g0104 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02897 | hp2 | a0001 | c0006 | t0013 | g0113 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02922 | hp1 | a0001 | c0001 | t0032 | g0175 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0368 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02965 | hp1 | a0001 | c0001 | t0046 | g0112 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02965 | hp2 | a0001 | c0001 | t0022 | g0325 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02970 | hp1 | a0001 | c0001 | t0017 | g0375 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02970 | hp2 | a0001 | c0001 | t0013 | g0307 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02976 | hp1 | a0001 | c0001 | t0013 | g0310 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02976 | hp2 | a0001 | c0001 | t0068 | g0189 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03017 | hp1 | a0001 | c0002 | t0008 | g0085 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03041 | hp1 | a0001 | c0006 | t0056 | g0305 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03098 | hp1 | a0001 | c0003 | t0005 | g0377 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03098 | hp2 | a0001 | c0001 | t0012 | g0374 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03130 | hp1 | a0001 | c0001 | t0016 | g0219 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0226 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03139 | hp1 | a0001 | c0002 | t0024 | g0340 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03139 | hp2 | a0001 | c0001 | t0017 | g0155 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03195 | hp1 | a0001 | c0002 | t0034 | g0185 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03195 | hp2 | a0001 | c0001 | t0035 | g0011 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03209 | hp1 | a0001 | c0001 | t0022 | g0313 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03209 | hp2 | a0001 | c0001 | t0014 | g0184 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0357 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03225 | hp2 | a0001 | c0006 | t0013 | g0304 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03239 | hp1 | a0001 | c0002 | t0008 | g0050 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03453 | hp1 | a0001 | c0003 | t0011 | g0180 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03453 | hp2 | a0001 | c0001 | t0021 | g0326 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03491 | hp1 | a0001 | c0003 | t0011 | g0080 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03492 | hp1 | a0001 | c0001 | t0015 | g0356 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03516 | hp1 | a0001 | c0001 | t0036 | g0334 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03516 | hp2 | a0001 | c0001 | t0061 | g0198 | AFR | ESN | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03540 | hp2 | a0001 | c0001 | t0017 | g0017 | AFR | GWD | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0021 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03579 | hp2 | a0001 | c0001 | t0014 | g0369 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03654 | hp2 | a0001 | c0003 | t0005 | g0119 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03669 | hp1 | a0001 | c0002 | t0009 | g0054 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03669 | hp2 | a0001 | c0002 | t0024 | g0350 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03688 | hp2 | a0001 | c0003 | t0016 | g0196 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03704 | hp1 | a0001 | c0003 | t0030 | g0099 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03704 | hp2 | a0001 | c0002 | t0043 | g0331 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0133 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0241 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03831 | hp2 | a0002 | c0009 | t0015 | g0366 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03834 | hp2 | a0001 | c0003 | t0005 | g0286 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03927 | hp1 | a0001 | c0003 | t0005 | g0302 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03927 | hp2 | a0001 | c0001 | t0027 | g0328 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03942 | hp1 | a0001 | c0003 | t0005 | g0150 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03942 | hp2 | a0001 | c0001 | t0007 | g0057 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04115 | hp1 | a0001 | c0001 | t0007 | g0051 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04115 | hp2 | a0001 | c0001 | t0015 | g0358 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04184 | hp1 | a0001 | c0003 | t0040 | g0351 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04184 | hp2 | a0001 | c0001 | t0007 | g0323 | SAS | BEB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04199 | hp1 | a0001 | c0001 | t0015 | g0338 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04199 | hp2 | a0001 | c0003 | t0005 | g0285 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04204 | hp1 | a0001 | c0001 | t0010 | g0361 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04228 | hp1 | a0001 | c0001 | t0027 | g0317 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18522 | hp1 | a0001 | c0002 | t0012 | g0227 | AFR | YRI | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18522 | hp2 | a0001 | c0001 | t0036 | g0365 | AFR | YRI | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18612 | hp2 | a0001 | c0002 | t0006 | g0115 | EAS | CHB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18747 | hp1 | a0001 | c0003 | t0077 | g0270 | EAS | CHB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18747 | hp2 | a0001 | c0002 | t0006 | g0243 | EAS | CHB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18906 | hp1 | a0001 | c0002 | t0012 | g0216 | AFR | YRI | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18906 | hp2 | a0001 | c0001 | t0019 | g0337 | AFR | YRI | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18939 | hp1 | a0001 | c0002 | t0004 | g0248 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18939 | hp2 | a0001 | c0001 | t0026 | g0007 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18941 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18949 | hp2 | a0001 | c0001 | t0006 | g0245 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18951 | hp2 | a0001 | c0002 | t0009 | g0070 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18952 | hp2 | a0001 | c0002 | t0009 | g0041 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18953 | hp2 | a0001 | c0002 | t0009 | g0089 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18957 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18959 | hp2 | a0001 | c0002 | t0006 | g0234 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18960 | hp2 | a0001 | c0002 | t0008 | g0087 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18961 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18962 | hp1 | a0001 | c0002 | t0008 | g0084 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18962 | hp2 | a0001 | c0001 | t0055 | g0303 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18964 | hp2 | a0001 | c0002 | t0025 | g0348 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18965 | hp1 | a0001 | c0001 | t0010 | g0364 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18966 | hp2 | a0001 | c0004 | t0005 | g0293 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18967 | hp1 | a0001 | c0002 | t0006 | g0296 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18968 | hp1 | a0001 | c0002 | t0006 | g0294 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18970 | hp1 | a0001 | c0002 | t0008 | g0034 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18970 | hp2 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18971 | hp2 | a0001 | c0001 | t0029 | g0061 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18973 | hp1 | a0001 | c0001 | t0042 | g0072 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18974 | hp2 | a0001 | c0002 | t0004 | g0206 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18975 | hp2 | a0001 | c0002 | t0004 | g0251 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0315 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18977 | hp2 | a0001 | c0004 | t0011 | g0038 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18979 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18980 | hp1 | a0002 | c0005 | t0006 | g0336 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18980 | hp2 | a0001 | c0002 | t0006 | g0264 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18981 | hp1 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18981 | hp2 | a0001 | c0002 | t0009 | g0095 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18983 | hp1 | a0001 | c0003 | t0011 | g0060 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18983 | hp2 | a0001 | c0001 | t0010 | g0363 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18984 | hp1 | a0001 | c0002 | t0006 | g0275 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18985 | hp2 | a0001 | c0002 | t0008 | g0035 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18988 | hp2 | a0001 | c0002 | t0004 | g0233 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18990 | hp1 | a0001 | c0001 | t0026 | g0007 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18990 | hp2 | a0001 | c0002 | t0009 | g0068 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18991 | hp1 | a0001 | c0002 | t0008 | g0026 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18992 | hp1 | a0001 | c0002 | t0004 | g0284 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18994 | hp2 | a0001 | c0002 | t0009 | g0076 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18995 | hp1 | a0001 | c0002 | t0008 | g0081 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18997 | hp1 | a0001 | c0004 | t0005 | g0157 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18997 | hp2 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18998 | hp2 | a0001 | c0002 | t0006 | g0260 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18999 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19000 | hp2 | a0001 | c0001 | t0029 | g0091 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19001 | hp1 | a0001 | c0001 | t0050 | g0029 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19001 | hp2 | a0001 | c0002 | t0009 | g0105 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19003 | hp1 | a0001 | c0001 | t0007 | g0055 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19003 | hp2 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19004 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19005 | hp2 | a0001 | c0002 | t0006 | g0114 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19006 | hp2 | a0001 | c0002 | t0025 | g0359 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19009 | hp1 | a0001 | c0004 | t0011 | g0062 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19010 | hp2 | a0001 | c0002 | t0044 | g0046 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19011 | hp2 | a0001 | c0001 | t0009 | g0069 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19012 | hp1 | a0001 | c0002 | t0009 | g0009 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19012 | hp2 | a0001 | c0002 | t0004 | g0261 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19030 | hp1 | a0001 | c0001 | t0012 | g0217 | AFR | LWK | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19030 | hp2 | a0001 | c0002 | t0019 | g0346 | AFR | LWK | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19043 | hp1 | a0001 | c0001 | t0014 | g0183 | AFR | LWK | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19043 | hp2 | a0001 | c0001 | t0060 | g0205 | AFR | LWK | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19055 | hp2 | a0002 | c0005 | t0005 | g0018 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19056 | hp1 | a0001 | c0002 | t0006 | g0246 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19056 | hp2 | a0001 | c0001 | t0007 | g0028 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19058 | hp1 | a0002 | c0005 | t0005 | g0244 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19060 | hp1 | a0001 | c0002 | t0004 | g0283 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19060 | hp2 | a0001 | c0002 | t0006 | g0335 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19062 | hp1 | a0001 | c0002 | t0004 | g0280 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19062 | hp2 | a0001 | c0002 | t0009 | g0037 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19063 | hp2 | a0001 | c0002 | t0006 | g0269 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19066 | hp2 | a0001 | c0002 | t0009 | g0009 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19068 | hp2 | a0001 | c0002 | t0008 | g0083 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19075 | hp2 | a0001 | c0004 | t0011 | g0078 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19077 | hp2 | a0001 | c0002 | t0006 | g0295 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19079 | hp1 | a0001 | c0002 | t0009 | g0108 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19079 | hp2 | a0001 | c0004 | t0005 | g0235 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19082 | hp2 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19083 | hp1 | a0001 | c0002 | t0008 | g0082 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19083 | hp2 | a0001 | c0007 | t0070 | g0262 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19084 | hp1 | a0001 | c0010 | t0001 | g0278 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19084 | hp2 | a0002 | c0005 | t0005 | g0018 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19085 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19085 | hp2 | a0002 | c0005 | t0009 | g0033 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19086 | hp2 | a0001 | c0004 | t0011 | g0314 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19090 | hp1 | a0001 | c0004 | t0011 | g0096 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA20129 | hp1 | a0001 | c0001 | t0075 | g0195 | AFR | ASW | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA20129 | hp2 | a0001 | c0001 | t0035 | g0011 | AFR | ASW | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA20752 | hp1 | a0001 | c0001 | t0008 | g0333 | EUR | TSI | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA20752 | hp2 | a0001 | c0003 | t0018 | g0140 | EUR | TSI | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA20905 | hp1 | a0001 | c0001 | t0010 | g0339 | SAS | GIH | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA20905 | hp2 | a0001 | c0003 | t0020 | g0362 | SAS | GIH | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02109 | hp1 | a0001 | c0001 | t0014 | g0188 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02109 | hp2 | a0001 | c0001 | t0065 | g0202 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02486 | hp1 | a0001 | c0001 | t0072 | g0370 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02486 | hp2 | a0001 | c0001 | t0062 | g0201 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02559 | hp1 | a0001 | c0001 | t0074 | g0223 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG02559 | hp2 | a0001 | c0001 | t0038 | g0200 | AFR | ACB | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0187 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG03471 | hp2 | a0001 | c0001 | t0064 | g0204 | AFR | MSL | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG06807 | hp1 | a0001 | c0001 | t0081 | g0372 | AFR | USA | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
HG06807 | hp2 | a0001 | c0001 | t0063 | g0203 | AFR | USA | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18955 | hp1 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA21309 | hp1 | a0001 | c0001 | t0012 | g0367 | AFR | LWK | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
NA21309 | hp2 | a0001 | c0001 | t0033 | g0220 | AFR | LWK | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
homoSapiens | chm13v2 | a0001 | c0003 | t0058 | g0330 | REF | REF | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
homoSapiens | grch38p0 | a0001 | c0001 | t0041 | g0347 | REF | REF | EHF_chr11_34616093_34668288 | EHF | chr11 | 34616093 | 34668288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:34646628 | C | T | 1 | a0002 | 10 | HG00423.hp2 HG00735.hp1 HG01978.hp1 others(7): Show |
missense_variant | MODERATE | c.287C>T | p.Ala96Val | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/9 | 426/5399 | 287/903 | 96/300 | chr11 | 34646628 | |||
chr11:34651602 | G | A | 1 | a0003 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.467G>A | p.Ser156Asn | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 5/9 | 606/5399 | 467/903 | 156/300 | chr11 | 34651602 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:34646584 | C | T | 1 | a0001c0010 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.243C>T | p.Asn81Asn | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/9 | 382/5399 | 243/903 | 81/300 | chr11 | 34646584 | |||
chr11:34646596 | C | T | 2 | a0001c0002 a0001c0004 |
102 | HG00280.hp2 HG00408.hp1 HG00621.hp2 others(99): Show |
synonymous_variant | LOW | c.255C>T | p.Leu85Leu | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/9 | 394/5399 | 255/903 | 85/300 | chr11 | 34646596 | |||
chr11:34646614 | G | A | 1 | a0001c0007 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.273G>A | p.Gln91Gln | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/9 | 412/5399 | 273/903 | 91/300 | chr11 | 34646614 | |||
chr11:34649059 | C | T | 1 | a0001c0006 | 6 | HG02280.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
synonymous_variant | LOW | c.384C>T | p.Val128Val | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/9 | 523/5399 | 384/903 | 128/300 | chr11 | 34649059 | |||
chr11:34658853 | T | A | 3 | a0001c0003 a0001c0004 a0002c0005 |
49 | HG00423.hp2 HG00733.hp2 HG00735.hp1 others(46): Show |
synonymous_variant | LOW | c.825T>A | p.Ile275Ile | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 964/5399 | 825/903 | 275/300 | chr11 | 34658853 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:34621121 | A | G | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(48): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
5_prime_UTR_variant | MODIFIER | c.-111A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/9 | 21510 | chr11 | 34621121 | ||||||
chr11:34621181 | A | T | 80 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(77): Show |
367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
5_prime_UTR_variant | MODIFIER | c.-51A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/9 | 21450 | chr11 | 34621181 | ||||||
chr11:34658934 | C | A | 1 | a0001c0001t0026 | 2 | NA18939.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3 | chr11 | 34658934 | ||||||
chr11:34659046 | G | A | 1 | a0001c0001t0032 | 2 | HG02145.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 115 | chr11 | 34659046 | ||||||
chr11:34659051 | C | A | 19 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(16): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*120C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 120 | chr11 | 34659051 | ||||||
chr11:34659087 | G | A | 98 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(95): Show |
404 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(401): Show |
3_prime_UTR_variant | MODIFIER | c.*156G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 156 | chr11 | 34659087 | ||||||
chr11:34659306 | G | T | 41 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(38): Show |
178 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*375G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 375 | chr11 | 34659306 | ||||||
chr11:34659429 | G | A | 1 | a0001c0002t0071 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 498 | chr11 | 34659429 | ||||||
chr11:34659489 | A | G | 2 | a0001c0001t0075 a0001c0006t0056 |
2 | HG03041.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*558A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 558 | chr11 | 34659489 | ||||||
chr11:34659604 | G | A | 5 | a0001c0001t0013 a0001c0001t0067 a0001c0006t0013 others(2): Show |
10 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*673G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 673 | chr11 | 34659604 | ||||||
chr11:34659737 | A | G | 1 | a0001c0001t0055 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 806 | chr11 | 34659737 | ||||||
chr11:34659744 | C | T | 2 | a0001c0002t0023 a0001c0002t0048 |
4 | HG01074.hp1 HG01952.hp2 HG01975.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*813C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 813 | chr11 | 34659744 | ||||||
chr11:34659794 | A | G | 3 | a0001c0003t0018 a0001c0003t0030 a0001c0003t0040 |
8 | HG01074.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*863A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 863 | chr11 | 34659794 | ||||||
chr11:34659915 | A | G | 23 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0012 others(20): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*984A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 984 | chr11 | 34659915 | ||||||
chr11:34659917 | A | C | 1 | a0001c0001t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*986A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 986 | chr11 | 34659917 | ||||||
chr11:34659935 | C | T | 1 | a0001c0001t0061 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1004C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1004 | chr11 | 34659935 | ||||||
chr11:34660045 | A | G | 2 | a0001c0001t0054 a0001c0001t0080 |
2 | HG02647.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1114A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1114 | chr11 | 34660045 | ||||||
chr11:34660077 | T | C | 1 | a0001c0001t0072 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1146T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1146 | chr11 | 34660077 | ||||||
chr11:34660130 | G | A | 24 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0012 others(21): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1199G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1199 | chr11 | 34660130 | ||||||
chr11:34660214 | T | C | 12 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0072 others(9): Show |
54 | HG00597.hp1 HG00621.hp2 HG00741.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1283T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1283 | chr11 | 34660214 | ||||||
chr11:34660313 | G | A | 1 | a0001c0004t0049 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1382G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1382 | chr11 | 34660313 | ||||||
chr11:34660387 | A | G | 1 | a0001c0001t0079 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1456A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1456 | chr11 | 34660387 | ||||||
chr11:34660418 | A | T | 1 | a0001c0001t0066 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1487A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1487 | chr11 | 34660418 | ||||||
chr11:34660628 | A | G | 1 | a0001c0007t0070 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1697A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1697 | chr11 | 34660628 | ||||||
chr11:34660915 | T | C | 1 | a0001c0001t0074 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1984T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 1984 | chr11 | 34660915 | ||||||
chr11:34660948 | A | G | 6 | a0001c0001t0017 a0001c0001t0036 a0001c0001t0053 others(3): Show |
11 | HG01496.hp1 HG02109.hp2 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2017A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2017 | chr11 | 34660948 | ||||||
chr11:34661000 | T | C | 93 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(90): Show |
392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
3_prime_UTR_variant | MODIFIER | c.*2069T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2069 | chr11 | 34661000 | ||||||
chr11:34661022 | G | T | 1 | a0001c0001t0042 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2091G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2091 | chr11 | 34661022 | ||||||
chr11:34661215 | T | C | 2 | a0001c0001t0027 a0001c0001t0033 |
4 | HG00099.hp1 HG03927.hp2 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2284T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2284 | chr11 | 34661215 | ||||||
chr11:34661220 | C | T | 26 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0009 others(23): Show |
86 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2289C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2289 | chr11 | 34661220 | ||||||
chr11:34661221 | G | T | 1 | a0001c0002t0073 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2290G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2290 | chr11 | 34661221 | ||||||
chr11:34661331 | A | G | 1 | a0001c0002t0044 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2400A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2400 | chr11 | 34661331 | ||||||
chr11:34661415 | G | T | 13 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0015 others(10): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2484G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2484 | chr11 | 34661415 | ||||||
chr11:34661630 | G | A | 1 | a0001c0001t0057 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2699G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2699 | chr11 | 34661630 | ||||||
chr11:34661775 | TCACCTGT others(10): Show |
T | 1 | a0001c0003t0051 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2848_*2864delCTGT others(13): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2848 | INFO_REALIGN_3_PRIME | chr11 | 34661775 | |||||
chr11:34661779 | C | T | 1 | a0001c0001t0001 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2848C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 2848 | chr11 | 34661779 | ||||||
chr11:34661967 | C | G | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0010 others(13): Show |
116 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*3036C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3036 | chr11 | 34661967 | ||||||
chr11:34662031 | G | A | 21 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(18): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3100G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3100 | chr11 | 34662031 | ||||||
chr11:34662251 | T | C | 7 | a0001c0001t0013 a0001c0001t0035 a0001c0001t0062 others(4): Show |
13 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3320T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3320 | chr11 | 34662251 | ||||||
chr11:34662288 | C | G | 1 | a0001c0001t0050 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3357C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3357 | chr11 | 34662288 | ||||||
chr11:34662294 | C | T | 1 | a0001c0003t0078 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3363C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3363 | chr11 | 34662294 | ||||||
chr11:34662375 | G | A | 3 | a0001c0003t0051 a0001c0004t0052 a0002c0005t0076 |
3 | HG00733.hp2 HG00735.hp1 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3444G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3444 | chr11 | 34662375 | ||||||
chr11:34662376 | T | A | 1 | a0001c0001t0045 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3445T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3445 | chr11 | 34662376 | ||||||
chr11:34662484 | A | C | 1 | a0001c0003t0077 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3553A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3553 | chr11 | 34662484 | ||||||
chr11:34662496 | T | C | 1 | a0001c0001t0035 | 2 | HG03195.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3565T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3565 | chr11 | 34662496 | ||||||
chr11:34662615 | T | C | 2 | a0001c0001t0046 a0001c0002t0034 |
3 | HG02257.hp1 HG02965.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3684T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3684 | chr11 | 34662615 | ||||||
chr11:34662644 | T | C | 1 | a0001c0001t0029 | 2 | NA18971.hp2 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3713T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3713 | chr11 | 34662644 | ||||||
chr11:34662869 | A | G | 1 | a0001c0001t0028 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3938A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3938 | chr11 | 34662869 | ||||||
chr11:34662875 | T | C | 1 | a0001c0001t0069 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3944T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 3944 | chr11 | 34662875 | ||||||
chr11:34662996 | C | A | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0010 others(13): Show |
116 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*4065C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 4065 | chr11 | 34662996 | ||||||
chr11:34663034 | T | C | 1 | a0001c0002t0043 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4103T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 9/9 | 4103 | chr11 | 34663034 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:34621276 | T | C | 184 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(181): Show |
197 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.-4+48T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34621276 | |||||||
chr11:34621318 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-4+90C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34621318 | |||||||
chr11:34621419 | G | A | 1 | a0001c0001t0075g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-4+191G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34621419 | |||||||
chr11:34621451 | AT | A | 92 | a0001c0001t0002g0063 a0001c0001t0003g0008 a0001c0001t0003g0010 others(89): Show |
96 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-4+225delT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34621451 | ||||||
chr11:34621478 | T | TTTA | 14 | a0001c0001t0002g0378 a0001c0001t0004g0368 a0001c0001t0012g0021 others(11): Show |
15 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4+251_-4+253dupTT others(1): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34621478 | ||||||
chr11:34621677 | T | C | 1 | a0001c0003t0016g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-4+449T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34621677 | |||||||
chr11:34621895 | G | A | 347 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(344): Show |
375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.-4+667G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34621895 | |||||||
chr11:34622027 | G | A | 1 | a0001c0001t0066g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-4+799G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622027 | |||||||
chr11:34622174 | T | C | 254 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(251): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-4+946T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622174 | |||||||
chr11:34622184 | G | A | 14 | a0001c0001t0002g0378 a0001c0001t0004g0368 a0001c0001t0012g0021 others(11): Show |
15 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4+956G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622184 | |||||||
chr11:34622199 | C | T | 3 | a0001c0001t0003g0107 a0001c0001t0003g0109 a0001c0002t0009g0108 |
3 | NA18967.hp2 NA19007.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-4+971C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622199 | |||||||
chr11:34622233 | A | G | 139 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0209 others(136): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.-4+1005A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622233 | |||||||
chr11:34622257 | G | T | 2 | a0001c0002t0006g0335 a0002c0005t0006g0336 |
2 | NA18980.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-4+1029G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622257 | |||||||
chr11:34622356 | A | C | 2 | a0001c0001t0008g0106 a0001c0002t0009g0105 |
2 | NA18981.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-4+1128A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622356 | |||||||
chr11:34622408 | G | A | 84 | a0001c0001t0002g0063 a0001c0001t0003g0008 a0001c0001t0003g0010 others(81): Show |
88 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.-4+1180G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622408 | |||||||
chr11:34622433 | A | G | 1 | a0001c0001t0036g0334 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-4+1205A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622433 | |||||||
chr11:34622592 | G | A | 1 | a0001c0001t0019g0337 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-4+1364G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622592 | |||||||
chr11:34622616 | T | C | 254 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(251): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-4+1388T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622616 | |||||||
chr11:34622636 | G | T | 92 | a0001c0001t0002g0063 a0001c0001t0003g0008 a0001c0001t0003g0010 others(89): Show |
96 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-4+1408G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622636 | |||||||
chr11:34622659 | A | T | 1 | a0001c0004t0011g0096 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-4+1431A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622659 | |||||||
chr11:34622662 | TA | T | 31 | a0001c0001t0003g0306 a0001c0001t0003g0319 a0001c0001t0003g0322 others(28): Show |
32 | HG01081.hp2 HG01192.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.-4+1438delA | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34622662 | ||||||
chr11:34622686 | C | A | 1 | a0001c0001t0002g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-4+1458C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622686 | |||||||
chr11:34622846 | C | T | 193 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(190): Show |
206 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.-4+1618C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622846 | |||||||
chr11:34622852 | C | T | 1 | a0001c0003t0005g0302 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-4+1624C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622852 | |||||||
chr11:34622853 | G | A | 93 | a0001c0001t0002g0063 a0001c0001t0003g0008 a0001c0001t0003g0010 others(90): Show |
97 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-4+1625G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622853 | |||||||
chr11:34622907 | C | T | 93 | a0001c0001t0002g0063 a0001c0001t0003g0008 a0001c0001t0003g0010 others(90): Show |
97 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-4+1679C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622907 | |||||||
chr11:34622936 | C | T | 152 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0209 others(149): Show |
167 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.-4+1708C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622936 | |||||||
chr11:34622938 | C | T | 9 | a0001c0001t0038g0200 a0001c0001t0060g0205 a0001c0001t0061g0198 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+1710C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34622938 | |||||||
chr11:34623098 | G | GT | 7 | a0001c0001t0001g0193 a0001c0001t0001g0301 a0001c0001t0004g0192 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4+1879dupT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34623098 | ||||||
chr11:34623122 | G | T | 93 | a0001c0001t0002g0063 a0001c0001t0003g0008 a0001c0001t0003g0010 others(90): Show |
97 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-4+1894G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34623122 | |||||||
chr11:34623129 | A | G | 3 | a0001c0001t0007g0332 a0001c0001t0008g0333 a0001c0002t0043g0331 |
3 | HG01081.hp2 HG03704.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-4+1901A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34623129 | |||||||
chr11:34623283 | A | G | 254 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(251): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-4+2055A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34623283 | |||||||
chr11:34623329 | A | G | 1 | a0001c0001t0036g0365 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-4+2101A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34623329 | |||||||
chr11:34623571 | A | G | 1 | a0001c0001t0002g0300 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-4+2343A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34623571 | |||||||
chr11:34623616 | G | A | 4 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0007g0023 others(1): Show |
5 | NA18939.hp2 NA18988.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+2388G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34623616 | |||||||
chr11:34623621 | C | T | 12 | a0001c0001t0002g0378 a0001c0001t0012g0021 a0001c0001t0012g0374 others(9): Show |
13 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4+2393C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34623621 | |||||||
chr11:34623656 | C | T | 93 | a0001c0001t0002g0063 a0001c0001t0003g0008 a0001c0001t0003g0010 others(90): Show |
97 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-4+2428C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34623656 | |||||||
chr11:34623714 | T | C | 1 | a0001c0001t0035g0011 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-4+2486T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34623714 | |||||||
chr11:34623932 | CT | C | 5 | a0001c0001t0001g0209 a0001c0001t0002g0208 a0001c0002t0001g0207 others(2): Show |
8 | NA18941.hp2 NA18961.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4+2708delT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34623932 | ||||||
chr11:34624089 | A | G | 31 | a0001c0001t0003g0306 a0001c0001t0003g0319 a0001c0001t0003g0322 others(28): Show |
32 | HG01081.hp2 HG01192.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.-4+2861A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624089 | |||||||
chr11:34624150 | T | C | 10 | a0001c0001t0012g0021 a0001c0001t0012g0374 a0001c0001t0014g0369 others(7): Show |
11 | HG01243.hp1 HG01496.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+2922T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624150 | |||||||
chr11:34624454 | T | C | 1 | a0001c0006t0013g0304 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-4+3226T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624454 | |||||||
chr11:34624461 | T | C | 2 | a0001c0001t0010g0339 a0001c0001t0015g0338 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-4+3233T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624461 | |||||||
chr11:34624618 | C | A | 3 | a0001c0001t0046g0112 a0001c0006t0013g0111 a0001c0006t0013g0113 |
3 | HG02896.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-4+3390C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624618 | |||||||
chr11:34624645 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-4+3417A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624645 | |||||||
chr11:34624715 | C | T | 8 | a0001c0001t0014g0184 a0001c0001t0014g0187 a0001c0001t0014g0188 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+3487C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624715 | |||||||
chr11:34624825 | C | T | 8 | a0001c0001t0014g0184 a0001c0001t0014g0187 a0001c0001t0014g0188 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+3597C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624825 | |||||||
chr11:34624832 | C | G | 8 | a0001c0001t0014g0184 a0001c0001t0014g0187 a0001c0001t0014g0188 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+3604C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624832 | |||||||
chr11:34624907 | T | G | 116 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(113): Show |
126 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(123): Show |
intron_variant | MODIFIER | c.-4+3679T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624907 | |||||||
chr11:34624955 | G | A | 3 | a0001c0001t0046g0112 a0001c0006t0013g0111 a0001c0006t0013g0113 |
3 | HG02896.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-4+3727G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34624955 | |||||||
chr11:34625212 | G | GT | 117 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(114): Show |
127 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.-4+3984_-4+3985ins others(1): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34625212 | |||||||
chr11:34625335 | G | A | 72 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(69): Show |
80 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.-4+4107G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34625335 | |||||||
chr11:34625384 | A | T | 1 | a0001c0001t0002g0297 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-4+4156A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34625384 | |||||||
chr11:34625386 | G | A | 2 | a0001c0002t0006g0114 a0001c0002t0006g0115 |
2 | NA18612.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-4+4158G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34625386 | |||||||
chr11:34625484 | T | C | 9 | a0001c0001t0038g0200 a0001c0001t0060g0205 a0001c0001t0061g0198 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+4256T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34625484 | |||||||
chr11:34625532 | C | A | 3 | a0001c0001t0038g0200 a0001c0001t0061g0198 a0001c0006t0059g0199 |
3 | HG02280.hp2 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-4+4304C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34625532 | |||||||
chr11:34625615 | C | G | 4 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0003t0018g0005 others(1): Show |
6 | HG01167.hp2 HG01169.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4+4387C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34625615 | |||||||
chr11:34625833 | AC | A | 9 | a0001c0001t0038g0200 a0001c0001t0060g0205 a0001c0001t0061g0198 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+4608delC | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34625833 | ||||||
chr11:34625981 | G | C | 107 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(104): Show |
116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-4+4753G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34625981 | |||||||
chr11:34626139 | A | G | 1 | a0001c0001t0075g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-4+4911A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34626139 | |||||||
chr11:34626140 | A | T | 1 | a0001c0002t0048g0329 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-4+4912A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34626140 | |||||||
chr11:34626219 | G | T | 5 | a0001c0002t0006g0292 a0001c0002t0006g0294 a0001c0002t0006g0295 others(2): Show |
5 | HG02129.hp2 NA18966.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+4991G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34626219 | |||||||
chr11:34626431 | T | A | 102 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(99): Show |
111 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.-4+5203T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34626431 | |||||||
chr11:34626442 | A | T | 145 | a0001c0001t0001g0209 a0001c0001t0001g0263 a0001c0001t0001g0265 others(142): Show |
153 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-4+5214A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34626442 | |||||||
chr11:34627068 | C | T | 102 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(99): Show |
111 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.-4+5840C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627068 | |||||||
chr11:34627093 | T | G | 4 | a0001c0001t0007g0097 a0001c0001t0007g0098 a0001c0003t0030g0099 others(1): Show |
4 | HG01074.hp2 HG01361.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+5865T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627093 | |||||||
chr11:34627112 | T | G | 2 | a0001c0001t0003g0025 a0001c0002t0008g0026 |
2 | NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-4+5884T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627112 | |||||||
chr11:34627112 | T | TTG | 134 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0215 others(131): Show |
146 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.-4+5915_-4+5916dup others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34627112 | ||||||
chr11:34627112 | T | TTGTG | 47 | a0001c0001t0001g0209 a0001c0001t0001g0263 a0001c0001t0001g0265 others(44): Show |
51 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.-4+5913_-4+5916dup others(4): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34627112 | ||||||
chr11:34627112 | T | TTGTGTG | 11 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0291 others(8): Show |
12 | HG02132.hp1 HG03834.hp2 HG04199.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+5911_-4+5916dup others(6): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34627112 | ||||||
chr11:34627112 | TTG | T | 45 | a0001c0001t0002g0378 a0001c0001t0003g0306 a0001c0001t0003g0319 others(42): Show |
47 | HG01081.hp2 HG01192.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-4+5915_-4+5916del others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34627112 | ||||||
chr11:34627112 | TTGTGTGT others(1): Show |
T | 101 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(98): Show |
110 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.-4+5909_-4+5916del others(8): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34627112 | ||||||
chr11:34627230 | T | C | 2 | a0001c0003t0005g0285 a0001c0003t0005g0286 |
2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-4+6002T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627230 | |||||||
chr11:34627329 | G | A | 3 | a0001c0001t0046g0112 a0001c0006t0013g0111 a0001c0006t0013g0113 |
3 | HG02896.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-4+6101G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627329 | |||||||
chr11:34627531 | A | T | 1 | a0001c0004t0049g0086 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-4+6303A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627531 | |||||||
chr11:34627574 | A | G | 1 | a0001c0002t0008g0085 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-4+6346A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627574 | |||||||
chr11:34627645 | C | G | 43 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0159 others(40): Show |
47 | HG00735.hp2 HG01123.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.-4+6417C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627645 | |||||||
chr11:34627759 | C | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0222 others(46): Show |
58 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-4+6531C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627759 | |||||||
chr11:34627851 | C | A | 1 | a0001c0002t0009g0105 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-4+6623C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627851 | |||||||
chr11:34627984 | T | C | 2 | a0001c0001t0019g0341 a0001c0002t0024g0340 |
2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-4+6756T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34627984 | |||||||
chr11:34628262 | A | C | 1 | a0001c0001t0036g0365 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-4+7034A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628262 | |||||||
chr11:34628262 | A | G | 1 | a0001c0002t0004g0284 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-4+7034A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628262 | |||||||
chr11:34628280 | C | T | 25 | a0001c0001t0001g0006 a0001c0001t0001g0232 a0001c0001t0001g0236 others(22): Show |
28 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-4+7052C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628280 | |||||||
chr11:34628352 | T | A | 1 | a0001c0002t0071g0116 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-4+7124T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628352 | |||||||
chr11:34628653 | G | A | 55 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(52): Show |
60 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-4+7425G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628653 | |||||||
chr11:34628734 | G | C | 50 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0159 others(47): Show |
54 | HG00735.hp2 HG01123.hp1 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.-4+7506G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628734 | |||||||
chr11:34628772 | C | T | 1 | a0001c0001t0010g0363 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-4+7544C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628772 | |||||||
chr11:34628840 | C | T | 1 | a0001c0001t0036g0365 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-4+7612C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628840 | |||||||
chr11:34628852 | C | T | 50 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0159 others(47): Show |
54 | HG00735.hp2 HG01123.hp1 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.-4+7624C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628852 | |||||||
chr11:34628903 | A | G | 2 | a0001c0001t0001g0229 a0001c0002t0034g0230 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-4+7675A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34628903 | |||||||
chr11:34629055 | T | A | 3 | a0001c0001t0002g0300 a0001c0001t0012g0217 a0001c0002t0012g0216 |
3 | HG03540.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-4+7827T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629055 | |||||||
chr11:34629151 | C | T | 5 | a0001c0001t0012g0226 a0001c0001t0017g0017 a0001c0001t0036g0334 others(2): Show |
6 | HG02615.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+7923C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629151 | |||||||
chr11:34629152 | G | A | 22 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0159 others(19): Show |
25 | HG00735.hp2 HG01123.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.-4+7924G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629152 | |||||||
chr11:34629156 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-4+7928T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629156 | |||||||
chr11:34629156 | T | C | 49 | a0001c0001t0001g0153 a0001c0001t0001g0159 a0001c0001t0001g0160 others(46): Show |
53 | HG00735.hp2 HG01123.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.-4+7928T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629156 | |||||||
chr11:34629192 | A | C | 8 | a0001c0001t0014g0184 a0001c0001t0014g0187 a0001c0001t0014g0188 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4+7964A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629192 | |||||||
chr11:34629217 | A | G | 262 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(259): Show |
280 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.-4+7989A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629217 | |||||||
chr11:34629280 | G | T | 7 | a0001c0001t0060g0205 a0001c0001t0061g0198 a0001c0001t0062g0201 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+8052G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629280 | |||||||
chr11:34629293 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-4+8065G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629293 | |||||||
chr11:34629365 | G | A | 41 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0159 others(38): Show |
45 | HG00735.hp2 HG01123.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.-4+8137G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629365 | |||||||
chr11:34629409 | A | G | 1 | a0001c0001t0035g0011 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-4+8181A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34629409 | |||||||
chr11:34629859 | GT | G | 218 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(215): Show |
231 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.-4+8641delT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34629859 | ||||||
chr11:34630060 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-4+8832A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630060 | |||||||
chr11:34630142 | AACTTTGA others(10): Show |
A | 1 | a0001c0002t0004g0283 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-4+8916_-4+8932del others(17): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34630142 | ||||||
chr11:34630330 | T | G | 1 | a0001c0001t0066g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-4+9102T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630330 | |||||||
chr11:34630588 | A | T | 3 | a0001c0001t0010g0361 a0001c0003t0020g0362 a0002c0009t0015g0366 |
3 | HG03831.hp2 HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-4+9360A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630588 | |||||||
chr11:34630643 | C | T | 1 | a0001c0001t0010g0360 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-4+9415C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630643 | |||||||
chr11:34630670 | A | G | 1 | a0001c0001t0075g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-4+9442A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630670 | |||||||
chr11:34630677 | G | T | 14 | a0001c0001t0002g0378 a0001c0001t0004g0368 a0001c0001t0012g0021 others(11): Show |
15 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4+9449G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630677 | |||||||
chr11:34630686 | A | ATTTT | 342 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(339): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.-4+9459_-4+9460ins others(4): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34630686 | ||||||
chr11:34630712 | T | A | 1 | a0001c0001t0002g0378 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-4+9484T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630712 | |||||||
chr11:34630761 | C | T | 32 | a0001c0001t0001g0215 a0001c0001t0003g0319 a0001c0001t0003g0322 others(29): Show |
33 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-4+9533C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630761 | |||||||
chr11:34630789 | C | T | 12 | a0001c0001t0002g0378 a0001c0001t0012g0021 a0001c0001t0012g0374 others(9): Show |
13 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-4+9561C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630789 | |||||||
chr11:34630807 | C | A | 3 | a0001c0001t0003g0306 a0001c0001t0013g0307 a0001c0006t0056g0305 |
3 | HG01192.hp1 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-4+9579C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630807 | |||||||
chr11:34630817 | C | T | 3 | a0001c0001t0046g0112 a0001c0006t0013g0111 a0001c0006t0013g0113 |
3 | HG02896.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-4+9589C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630817 | |||||||
chr11:34630853 | C | T | 2 | a0001c0001t0019g0337 a0001c0001t0038g0200 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-4+9625C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630853 | |||||||
chr11:34630887 | C | A | 3 | a0001c0001t0046g0112 a0001c0006t0013g0111 a0001c0006t0013g0113 |
3 | HG02896.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-4+9659C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630887 | |||||||
chr11:34630938 | C | A | 340 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(337): Show |
368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.-4+9710C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630938 | |||||||
chr11:34630985 | C | A | 1 | a0001c0001t0036g0365 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-4+9757C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34630985 | |||||||
chr11:34631044 | T | A | 1 | a0001c0002t0006g0231 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-4+9816T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631044 | |||||||
chr11:34631052 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-4+9824A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631052 | |||||||
chr11:34631186 | C | A | 1 | a0001c0001t0010g0342 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-4+9958C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631186 | |||||||
chr11:34631276 | C | A | 1 | a0001c0001t0036g0365 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-4+10048C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631276 | |||||||
chr11:34631283 | C | T | 1 | a0001c0001t0003g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-4+10055C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631283 | |||||||
chr11:34631284 | G | A | 1 | a0001c0003t0020g0343 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-4+10056G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631284 | |||||||
chr11:34631429 | C | T | 1 | a0001c0001t0033g0252 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-4+10201C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631429 | |||||||
chr11:34631476 | T | C | 32 | a0001c0001t0001g0215 a0001c0001t0003g0319 a0001c0001t0003g0322 others(29): Show |
33 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-4+10248T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631476 | |||||||
chr11:34631577 | G | A | 88 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0215 others(85): Show |
98 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-4+10349G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631577 | |||||||
chr11:34631598 | G | A | 2 | a0001c0002t0006g0335 a0002c0005t0006g0336 |
2 | NA18980.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-4+10370G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631598 | |||||||
chr11:34631621 | A | C | 2 | a0001c0001t0004g0368 a0001c0001t0012g0367 |
2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-4+10393A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631621 | |||||||
chr11:34631670 | G | A | 3 | a0001c0001t0007g0332 a0001c0001t0008g0333 a0001c0002t0043g0331 |
3 | HG01081.hp2 HG03704.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-4+10442G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631670 | |||||||
chr11:34631730 | G | A | 2 | a0001c0002t0004g0261 a0001c0002t0006g0260 |
2 | NA18998.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-4+10502G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631730 | |||||||
chr11:34631844 | G | T | 1 | a0001c0006t0059g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-4+10616G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631844 | |||||||
chr11:34631862 | G | C | 1 | a0001c0001t0054g0308 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-4+10634G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34631862 | |||||||
chr11:34632007 | G | A | 1 | a0001c0001t0075g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-3-10621G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632007 | |||||||
chr11:34632102 | G | A | 1 | a0001c0001t0062g0201 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3-10526G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632102 | |||||||
chr11:34632144 | G | A | 3 | a0001c0001t0007g0097 a0001c0001t0007g0098 a0001c0003t0030g0100 |
3 | HG01074.hp2 HG01361.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-3-10484G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632144 | |||||||
chr11:34632224 | T | G | 36 | a0001c0001t0001g0215 a0001c0001t0003g0306 a0001c0001t0003g0319 others(33): Show |
37 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3-10404T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632224 | |||||||
chr11:34632387 | A | G | 2 | a0001c0001t0019g0337 a0001c0001t0038g0200 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-3-10241A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632387 | |||||||
chr11:34632610 | A | AG | 5 | a0001c0001t0031g0179 a0001c0001t0045g0181 a0001c0001t0053g0177 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-10016dupG | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34632610 | ||||||
chr11:34632809 | G | C | 2 | a0001c0001t0001g0232 a0001c0002t0004g0233 |
2 | NA18988.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-3-9819G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632809 | |||||||
chr11:34632820 | T | A | 2 | a0001c0001t0003g0027 a0001c0004t0011g0096 |
2 | NA18993.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-3-9808T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632820 | |||||||
chr11:34632890 | G | A | 3 | a0001c0001t0013g0309 a0001c0001t0013g0310 a0001c0006t0013g0304 |
3 | HG01884.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-3-9738G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632890 | |||||||
chr11:34632947 | T | C | 1 | a0001c0001t0029g0091 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-3-9681T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632947 | |||||||
chr11:34632978 | C | T | 1 | a0001c0001t0013g0310 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-3-9650C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632978 | |||||||
chr11:34632993 | A | G | 4 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0007g0023 others(1): Show |
5 | NA18939.hp2 NA18988.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-9635A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34632993 | |||||||
chr11:34633173 | C | T | 3 | a0001c0002t0008g0082 a0001c0002t0008g0083 a0001c0002t0008g0084 |
3 | NA18962.hp1 NA19068.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-3-9455C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633173 | |||||||
chr11:34633254 | T | C | 2 | a0001c0002t0048g0329 a0002c0005t0011g0311 |
2 | HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-3-9374T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633254 | |||||||
chr11:34633390 | T | A | 9 | a0001c0001t0012g0374 a0001c0001t0014g0369 a0001c0001t0014g0371 others(6): Show |
9 | HG01243.hp1 HG01496.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3-9238T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633390 | |||||||
chr11:34633530 | A | T | 1 | a0001c0002t0008g0081 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-3-9098A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633530 | |||||||
chr11:34633535 | G | A | 2 | a0001c0001t0004g0368 a0001c0001t0012g0367 |
2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-3-9093G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633535 | |||||||
chr11:34633554 | G | T | 3 | a0001c0001t0046g0112 a0001c0006t0013g0111 a0001c0006t0013g0113 |
3 | HG02896.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-3-9074G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633554 | |||||||
chr11:34633605 | G | C | 8 | a0001c0001t0014g0184 a0001c0001t0014g0187 a0001c0001t0014g0188 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-9023G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633605 | |||||||
chr11:34633697 | C | G | 202 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(199): Show |
215 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.-3-8931C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633697 | |||||||
chr11:34633816 | A | G | 349 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(346): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.-3-8812A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633816 | |||||||
chr11:34633817 | G | T | 2 | a0001c0001t0019g0337 a0001c0001t0038g0200 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-3-8811G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633817 | |||||||
chr11:34633971 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0035g0011 a0001c0002t0012g0170 |
4 | HG02818.hp2 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-8657A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633971 | |||||||
chr11:34633993 | C | G | 1 | a0001c0001t0047g0101 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-3-8635C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34633993 | |||||||
chr11:34634190 | A | AT | 114 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0209 others(111): Show |
128 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-3-8429dupT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34634190 | ||||||
chr11:34634389 | T | G | 113 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(110): Show |
117 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-3-8239T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34634389 | |||||||
chr11:34634659 | A | G | 2 | a0001c0001t0019g0337 a0001c0001t0038g0200 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-3-7969A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34634659 | |||||||
chr11:34634927 | G | C | 1 | a0001c0001t0010g0344 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-3-7701G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34634927 | |||||||
chr11:34635050 | A | G | 67 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(64): Show |
73 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-3-7578A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635050 | |||||||
chr11:34635117 | G | A | 225 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(222): Show |
239 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-3-7511G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635117 | |||||||
chr11:34635450 | C | CT | 206 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0209 others(203): Show |
224 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-3-7160dupT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34635450 | ||||||
chr11:34635450 | C | CTT | 12 | a0001c0001t0001g0222 a0001c0001t0002g0256 a0001c0001t0003g0109 others(9): Show |
12 | HG01517.hp1 HG02145.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3-7161_-3-7160dup others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34635450 | ||||||
chr11:34635450 | C | CTTTTT | 53 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(50): Show |
58 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3-7164_-3-7160dup others(5): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34635450 | ||||||
chr11:34635450 | C | CTTTTTT | 12 | a0001c0001t0002g0378 a0001c0001t0012g0021 a0001c0001t0012g0374 others(9): Show |
13 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3-7165_-3-7160dup others(6): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34635450 | ||||||
chr11:34635492 | C | A | 27 | a0001c0001t0003g0319 a0001c0001t0003g0322 a0001c0001t0007g0020 others(24): Show |
28 | HG01081.hp2 HG01346.hp1 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.-3-7136C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635492 | |||||||
chr11:34635514 | C | T | 67 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(64): Show |
73 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-3-7114C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635514 | |||||||
chr11:34635597 | T | C | 112 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0209 others(109): Show |
126 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-3-7031T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635597 | |||||||
chr11:34635605 | T | G | 1 | a0001c0001t0001g0272 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-3-7023T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635605 | |||||||
chr11:34635674 | C | T | 152 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0152 others(149): Show |
170 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.-3-6954C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635674 | |||||||
chr11:34635701 | C | CT | 186 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0122 others(183): Show |
198 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.-3-6909dupT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34635701 | ||||||
chr11:34635701 | C | CTT | 9 | a0001c0001t0002g0221 a0001c0001t0003g0079 a0001c0001t0004g0368 others(6): Show |
9 | HG00597.hp2 HG01346.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-6910_-3-6909dup others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34635701 | ||||||
chr11:34635800 | T | C | 121 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(118): Show |
125 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.-3-6828T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635800 | |||||||
chr11:34635837 | G | A | 113 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(110): Show |
117 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-3-6791G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635837 | |||||||
chr11:34635838 | A | G | 375 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(372): Show |
406 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.-3-6790A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635838 | |||||||
chr11:34635868 | G | A | 12 | a0001c0001t0002g0378 a0001c0001t0012g0021 a0001c0001t0012g0374 others(9): Show |
13 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3-6760G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635868 | |||||||
chr11:34635869 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-3-6759G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635869 | |||||||
chr11:34635915 | C | G | 1 | a0001c0003t0005g0150 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-3-6713C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635915 | |||||||
chr11:34635929 | C | T | 1 | a0001c0001t0016g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-3-6699C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34635929 | |||||||
chr11:34636255 | A | T | 2 | a0001c0002t0006g0269 a0001c0003t0077g0270 |
2 | NA18747.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-3-6373A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636255 | |||||||
chr11:34636355 | T | C | 52 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(49): Show |
57 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-3-6273T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636355 | |||||||
chr11:34636445 | C | T | 85 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0209 others(82): Show |
98 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-3-6183C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636445 | |||||||
chr11:34636464 | A | G | 5 | a0001c0001t0060g0205 a0001c0001t0062g0201 a0001c0001t0063g0203 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-6164A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636464 | |||||||
chr11:34636529 | G | A | 212 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(209): Show |
225 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.-3-6099G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636529 | |||||||
chr11:34636653 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-3-5975A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636653 | |||||||
chr11:34636807 | C | A | 6 | a0001c0001t0001g0149 a0001c0001t0002g0172 a0001c0002t0001g0121 others(3): Show |
9 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3-5821C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636807 | |||||||
chr11:34636882 | A | C | 1 | a0001c0001t0038g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-3-5746A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636882 | |||||||
chr11:34636890 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0122 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-3-5738G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636890 | |||||||
chr11:34636990 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-3-5638T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34636990 | |||||||
chr11:34637017 | G | A | 1 | a0001c0002t0008g0034 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-3-5611G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637017 | |||||||
chr11:34637029 | C | CA | 71 | a0001c0001t0001g0152 a0001c0001t0001g0159 a0001c0001t0001g0160 others(68): Show |
79 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-3-5578dupA | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34637029 | ||||||
chr11:34637029 | C | CAA | 19 | a0001c0001t0001g0153 a0001c0001t0001g0229 a0001c0001t0002g0378 others(16): Show |
19 | HG00642.hp2 HG01243.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-3-5579_-3-5578dup others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34637029 | ||||||
chr11:34637029 | CA | C | 150 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0143 others(147): Show |
163 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.-3-5578delA | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34637029 | ||||||
chr11:34637038 | A | G | 1 | a0001c0002t0009g0105 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-3-5590A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637038 | |||||||
chr11:34637285 | G | T | 3 | a0001c0001t0003g0043 a0001c0001t0007g0028 a0001c0001t0007g0044 |
3 | NA18997.hp2 NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-3-5343G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637285 | |||||||
chr11:34637310 | G | A | 250 | a0001c0001t0001g0006 a0001c0001t0001g0149 a0001c0001t0001g0166 others(247): Show |
267 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.-3-5318G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637310 | |||||||
chr11:34637431 | T | C | 3 | a0001c0001t0001g0169 a0001c0001t0012g0374 a0001c0006t0013g0304 |
3 | HG03041.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-3-5197T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637431 | |||||||
chr11:34637454 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-3-5174G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637454 | |||||||
chr11:34637517 | G | A | 1 | a0001c0001t0047g0101 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-3-5111G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637517 | |||||||
chr11:34637633 | G | A | 1 | a0001c0001t0015g0358 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-3-4995G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637633 | |||||||
chr11:34637640 | T | A | 1 | a0001c0010t0001g0278 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-3-4988T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637640 | |||||||
chr11:34637899 | C | A | 3 | a0001c0001t0053g0177 a0001c0001t0065g0202 a0001c0003t0011g0180 |
3 | HG02109.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-3-4729C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637899 | |||||||
chr11:34637899 | C | CT | 129 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(126): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-3-4716dupT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34637899 | ||||||
chr11:34637912 | T | C | 4 | a0001c0001t0013g0309 a0001c0001t0013g0310 a0001c0001t0014g0371 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-4716T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637912 | |||||||
chr11:34637970 | C | T | 2 | a0001c0002t0025g0359 a0002c0005t0020g0349 |
2 | HG00423.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-3-4658C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637970 | |||||||
chr11:34637971 | G | A | 3 | a0001c0001t0053g0177 a0001c0001t0065g0202 a0001c0003t0011g0180 |
3 | HG02109.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-3-4657G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637971 | |||||||
chr11:34637979 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-3-4649G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637979 | |||||||
chr11:34637991 | T | G | 1 | a0001c0002t0006g0243 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-3-4637T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34637991 | |||||||
chr11:34638141 | A | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(119): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-3-4487A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34638141 | |||||||
chr11:34638260 | G | T | 175 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0132 others(172): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-3-4368G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34638260 | |||||||
chr11:34638286 | A | T | 174 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0132 others(171): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-3-4342A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34638286 | |||||||
chr11:34638464 | G | T | 1 | a0001c0003t0040g0351 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-3-4164G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34638464 | |||||||
chr11:34638530 | G | A | 3 | a0001c0001t0001g0263 a0001c0002t0006g0335 a0001c0002t0025g0348 |
3 | HG00438.hp2 NA18964.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-3-4098G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34638530 | |||||||
chr11:34638611 | G | C | 2 | a0001c0001t0001g0290 a0001c0001t0003g0036 |
2 | HG01978.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.-3-4017G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34638611 | |||||||
chr11:34638710 | T | C | 18 | a0001c0001t0001g0169 a0001c0001t0002g0378 a0001c0001t0010g0357 others(15): Show |
20 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-3-3918T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34638710 | |||||||
chr11:34638755 | G | A | 13 | a0001c0001t0001g0169 a0001c0001t0002g0378 a0001c0001t0010g0357 others(10): Show |
15 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.-3-3873G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34638755 | |||||||
chr11:34638934 | A | T | 14 | a0001c0001t0001g0131 a0001c0001t0001g0247 a0001c0001t0001g0249 others(11): Show |
15 | HG00558.hp2 HG00733.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3-3694A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34638934 | |||||||
chr11:34639071 | C | A | 156 | a0001c0001t0001g0132 a0001c0001t0001g0153 a0001c0001t0001g0166 others(153): Show |
166 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-3-3557C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639071 | |||||||
chr11:34639082 | C | G | 1 | a0001c0001t0014g0371 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-3-3546C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639082 | |||||||
chr11:34639112 | C | A | 9 | a0001c0001t0001g0144 a0001c0001t0001g0152 a0001c0001t0002g0013 others(6): Show |
10 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-3-3516C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639112 | |||||||
chr11:34639112 | C | T | 5 | a0001c0001t0001g0301 a0001c0001t0002g0378 a0001c0001t0031g0179 others(2): Show |
5 | HG01884.hp1 HG02056.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3-3516C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639112 | |||||||
chr11:34639203 | A | C | 3 | a0001c0001t0021g0103 a0001c0001t0021g0104 a0001c0001t0060g0205 |
3 | HG02895.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-3-3425A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639203 | |||||||
chr11:34639231 | A | AT | 104 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0131 others(101): Show |
111 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-3-3387dupT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34639231 | ||||||
chr11:34639231 | AT | A | 39 | a0001c0001t0001g0153 a0001c0001t0001g0222 a0001c0001t0001g0274 others(36): Show |
40 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-3-3387delT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34639231 | ||||||
chr11:34639447 | G | T | 9 | a0001c0001t0001g0169 a0001c0001t0002g0378 a0001c0001t0012g0021 others(6): Show |
11 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3-3181G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639447 | |||||||
chr11:34639475 | A | G | 60 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0131 others(57): Show |
63 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-3-3153A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639475 | |||||||
chr11:34639524 | C | T | 3 | a0001c0001t0007g0066 a0001c0001t0068g0189 a0001c0002t0004g0214 |
3 | HG02027.hp1 HG02738.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-3-3104C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639524 | |||||||
chr11:34639558 | C | G | 160 | a0001c0001t0001g0006 a0001c0001t0001g0118 a0001c0001t0001g0122 others(157): Show |
170 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.-3-3070C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639558 | |||||||
chr11:34639638 | T | C | 2 | a0001c0001t0047g0101 a0001c0001t0057g0178 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-3-2990T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639638 | |||||||
chr11:34639764 | C | T | 13 | a0001c0001t0001g0169 a0001c0001t0002g0378 a0001c0001t0012g0021 others(10): Show |
15 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3-2864C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639764 | |||||||
chr11:34639824 | C | G | 1 | a0001c0003t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-3-2804C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639824 | |||||||
chr11:34639892 | T | A | 1 | a0001c0001t0079g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-3-2736T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34639892 | |||||||
chr11:34640022 | C | CT | 90 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0131 others(87): Show |
95 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3-2593dupT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34640022 | ||||||
chr11:34640088 | T | G | 1 | a0001c0001t0014g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3-2540T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640088 | |||||||
chr11:34640252 | C | T | 1 | a0001c0002t0009g0108 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-3-2376C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640252 | |||||||
chr11:34640253 | G | A | 3 | a0001c0001t0031g0179 a0001c0001t0072g0370 a0001c0003t0005g0377 |
3 | HG02486.hp1 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-3-2375G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640253 | |||||||
chr11:34640306 | C | G | 39 | a0001c0001t0001g0153 a0001c0001t0001g0222 a0001c0001t0001g0274 others(36): Show |
40 | HG00423.hp2 HG01099.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-3-2322C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640306 | |||||||
chr11:34640545 | C | A | 1 | a0001c0002t0004g0206 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-3-2083C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640545 | |||||||
chr11:34640573 | G | A | 66 | a0001c0001t0001g0132 a0001c0001t0001g0153 a0001c0001t0001g0169 others(63): Show |
69 | HG00423.hp2 HG01099.hp1 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.-3-2055G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640573 | |||||||
chr11:34640647 | G | T | 1 | a0001c0001t0003g0094 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-3-1981G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640647 | |||||||
chr11:34640846 | A | G | 3 | a0001c0001t0001g0239 a0001c0001t0001g0301 a0001c0001t0003g0027 |
3 | HG00558.hp1 HG02056.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-3-1782A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640846 | |||||||
chr11:34640851 | C | G | 13 | a0001c0001t0001g0169 a0001c0001t0002g0378 a0001c0001t0012g0021 others(10): Show |
15 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3-1777C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640851 | |||||||
chr11:34640929 | A | G | 1 | a0001c0003t0005g0150 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-3-1699A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34640929 | |||||||
chr11:34641263 | T | A | 144 | a0001c0001t0001g0117 a0001c0001t0001g0159 a0001c0001t0001g0160 others(141): Show |
155 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.-3-1365T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34641263 | |||||||
chr11:34641315 | G | A | 1 | a0001c0001t0016g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-3-1313G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34641315 | |||||||
chr11:34641332 | T | C | 8 | a0001c0001t0014g0187 a0001c0001t0014g0188 a0001c0001t0017g0155 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-1296T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34641332 | |||||||
chr11:34641414 | A | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(275): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.-3-1214A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34641414 | |||||||
chr11:34641441 | C | G | 286 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(283): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-3-1187C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34641441 | |||||||
chr11:34641776 | G | A | 1 | a0001c0002t0004g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-3-852G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34641776 | |||||||
chr11:34642000 | T | C | 4 | a0001c0001t0001g0279 a0001c0001t0069g0277 a0001c0002t0004g0284 others(1): Show |
4 | HG02083.hp2 NA18952.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-628T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642000 | |||||||
chr11:34642007 | G | C | 1 | a0002c0005t0005g0244 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-3-621G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642007 | |||||||
chr11:34642143 | G | A | 4 | a0001c0001t0036g0334 a0001c0002t0039g0345 a0001c0006t0013g0111 others(1): Show |
4 | HG02055.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-485G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642143 | |||||||
chr11:34642145 | A | G | 4 | a0001c0001t0053g0177 a0001c0001t0057g0178 a0001c0001t0065g0202 others(1): Show |
4 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3-483A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642145 | |||||||
chr11:34642170 | G | A | 1 | a0001c0002t0019g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-458G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642170 | |||||||
chr11:34642173 | T | G | 2 | a0001c0001t0002g0378 a0001c0001t0016g0255 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-3-455T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642173 | |||||||
chr11:34642180 | C | T | 1 | a0001c0001t0038g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-3-448C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642180 | |||||||
chr11:34642290 | T | TA | 15 | a0001c0001t0001g0143 a0001c0001t0001g0263 a0001c0001t0001g0290 others(12): Show |
15 | HG00280.hp2 HG00438.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-3-328dupA | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34642290 | ||||||
chr11:34642301 | G | A | 71 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0149 others(68): Show |
73 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-3-327G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642301 | |||||||
chr11:34642301 | GA | G | 30 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0229 others(27): Show |
31 | HG01496.hp1 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.-3-316delA | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34642301 | ||||||
chr11:34642314 | T | C | 353 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(350): Show |
382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.-3-314T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642314 | |||||||
chr11:34642315 | G | A | 1 | a0001c0001t0007g0023 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-3-313G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642315 | |||||||
chr11:34642348 | G | A | 2 | a0001c0003t0030g0099 a0001c0003t0040g0351 |
2 | HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-3-280G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642348 | |||||||
chr11:34642487 | C | T | 1 | a0001c0002t0006g0276 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-3-141C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | chr11 | 34642487 | |||||||
chr11:34642532 | CTT | C | 3 | a0001c0002t0004g0136 a0001c0002t0048g0329 a0002c0009t0015g0366 |
3 | HG00621.hp2 HG01975.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-3-94_-3-93delTT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 34642532 | ||||||
chr11:34642816 | T | C | 11 | a0001c0001t0014g0184 a0001c0001t0014g0218 a0001c0001t0016g0219 others(8): Show |
11 | HG01891.hp1 HG02280.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+89T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34642816 | |||||||
chr11:34642874 | T | C | 6 | a0001c0001t0007g0055 a0001c0002t0008g0082 a0001c0002t0008g0083 others(3): Show |
6 | NA18962.hp1 NA18966.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.97+147T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34642874 | |||||||
chr11:34642905 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0010g0339 |
2 | HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.97+178A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34642905 | |||||||
chr11:34642975 | G | C | 4 | a0001c0001t0036g0334 a0001c0002t0039g0345 a0001c0006t0013g0111 others(1): Show |
4 | HG02055.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+248G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34642975 | |||||||
chr11:34642976 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.97+249G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34642976 | |||||||
chr11:34643065 | G | GGT | 65 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0149 others(62): Show |
68 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.97+339_97+340dupGT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643065 | ||||||
chr11:34643065 | G | GGTGT | 3 | a0001c0001t0001g0249 a0001c0001t0075g0195 a0001c0002t0009g0108 |
3 | NA19011.hp1 NA19079.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.97+340_97+341insGT others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643065 | ||||||
chr11:34643065 | G | GGTGTGTG others(1): Show |
3 | a0001c0001t0002g0378 a0001c0001t0032g0175 a0001c0001t0068g0189 |
3 | HG01884.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.97+340_97+341insGT others(6): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643065 | ||||||
chr11:34643065 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0032g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97+340_97+341insGT others(8): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643065 | ||||||
chr11:34643065 | GGTAT | G | 4 | a0001c0001t0057g0178 a0001c0001t0062g0201 a0001c0001t0064g0204 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+341_97+344delAT others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643065 | ||||||
chr11:34643068 | A | ATG | 20 | a0001c0001t0001g0229 a0001c0001t0002g0237 a0001c0001t0002g0300 others(17): Show |
23 | HG01515.hp1 HG01884.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.97+369_97+370dupGT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643068 | ||||||
chr11:34643068 | A | ATGTG | 6 | a0001c0001t0004g0368 a0001c0001t0017g0155 a0001c0001t0022g0313 others(3): Show |
6 | HG02922.hp2 HG03139.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.97+367_97+370dupGT others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643068 | ||||||
chr11:34643068 | A | ATGTGTG | 9 | a0001c0001t0012g0021 a0001c0001t0014g0183 a0001c0001t0014g0187 others(6): Show |
11 | HG02109.hp1 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+365_97+370dupGT others(4): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643068 | ||||||
chr11:34643068 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0038g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.97+361_97+370dupGT others(8): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643068 | ||||||
chr11:34643068 | A | G | 76 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0149 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.97+341A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643068 | |||||||
chr11:34643068 | ATG | A | 30 | a0001c0001t0002g0110 a0001c0001t0002g0238 a0001c0001t0002g0256 others(27): Show |
31 | HG00597.hp1 HG00741.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.97+369_97+370delGT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643068 | ||||||
chr11:34643068 | ATGTG | A | 3 | a0001c0001t0026g0007 a0001c0002t0008g0052 a0001c0004t0005g0235 |
4 | HG02135.hp1 NA18939.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+367_97+370delGT others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643068 | ||||||
chr11:34643106 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.97+379G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643106 | |||||||
chr11:34643191 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.97+464G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643191 | |||||||
chr11:34643329 | C | CCTGAATC others(11): Show |
1 | a0001c0001t0002g0137 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.97+616_97+633dupAA others(16): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643329 | ||||||
chr11:34643347 | TCTGAATC others(9): Show |
T | 16 | a0001c0001t0001g0281 a0001c0001t0001g0301 a0001c0001t0003g0027 others(13): Show |
19 | HG02056.hp2 HG02735.hp1 HG04199.hp2 others(16): Show |
intron_variant | MODIFIER | c.97+628_97+643delAA others(14): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34643347 | ||||||
chr11:34643377 | C | T | 1 | a0001c0002t0016g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97+650C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643377 | |||||||
chr11:34643378 | C | T | 18 | a0001c0001t0002g0110 a0001c0001t0002g0238 a0001c0001t0002g0256 others(15): Show |
19 | HG00597.hp1 HG00741.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.97+651C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643378 | |||||||
chr11:34643552 | C | T | 2 | a0001c0001t0017g0373 a0001c0001t0079g0228 |
2 | HG01496.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.97+825C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643552 | |||||||
chr11:34643600 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.97+873C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643600 | |||||||
chr11:34643674 | G | A | 1 | a0001c0003t0005g0285 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.97+947G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643674 | |||||||
chr11:34643974 | A | G | 1 | a0001c0001t0016g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.97+1247A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643974 | |||||||
chr11:34643986 | T | C | 1 | a0001c0002t0073g0282 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.97+1259T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34643986 | |||||||
chr11:34644136 | T | G | 11 | a0001c0001t0014g0184 a0001c0001t0014g0218 a0001c0001t0016g0219 others(8): Show |
11 | HG01891.hp1 HG02280.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+1409T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34644136 | |||||||
chr11:34644175 | G | C | 1 | a0001c0001t0003g0094 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.97+1448G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34644175 | |||||||
chr11:34644318 | C | T | 24 | a0001c0001t0001g0132 a0001c0001t0001g0222 a0001c0001t0002g0019 others(21): Show |
25 | HG00423.hp2 HG00741.hp1 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.97+1591C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34644318 | |||||||
chr11:34644378 | G | T | 75 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0149 others(72): Show |
78 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.97+1651G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34644378 | |||||||
chr11:34644516 | C | A | 63 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0149 others(60): Show |
65 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.97+1789C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34644516 | |||||||
chr11:34644587 | A | G | 1 | a0001c0001t0068g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98-1852A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34644587 | |||||||
chr11:34644682 | C | A | 3 | a0001c0001t0014g0218 a0001c0001t0016g0219 a0001c0001t0016g0379 |
3 | HG01891.hp1 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.98-1757C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34644682 | |||||||
chr11:34644689 | CT | C | 4 | a0001c0001t0001g0229 a0001c0001t0017g0373 a0001c0001t0019g0337 others(1): Show |
4 | HG01496.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1747delT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34644689 | ||||||
chr11:34644715 | G | C | 68 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0149 others(65): Show |
71 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.98-1724G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34644715 | |||||||
chr11:34644805 | T | C | 8 | a0001c0001t0014g0184 a0001c0001t0014g0218 a0001c0001t0016g0219 others(5): Show |
8 | HG01891.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.98-1634T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34644805 | |||||||
chr11:34645120 | A | G | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.98-1319A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645120 | |||||||
chr11:34645203 | G | A | 1 | a0001c0001t0047g0101 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.98-1236G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645203 | |||||||
chr11:34645238 | A | C | 2 | a0001c0002t0004g0283 a0001c0007t0070g0262 |
2 | NA19060.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.98-1201A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645238 | |||||||
chr11:34645303 | A | G | 66 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0122 others(63): Show |
70 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.98-1136A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645303 | |||||||
chr11:34645316 | C | T | 215 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(212): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.98-1123C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645316 | |||||||
chr11:34645356 | C | T | 375 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(372): Show |
406 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.98-1083C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645356 | |||||||
chr11:34645410 | C | T | 1 | a0001c0002t0019g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-1029C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645410 | |||||||
chr11:34645534 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.98-905G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645534 | |||||||
chr11:34645924 | T | C | 16 | a0001c0001t0012g0021 a0001c0001t0012g0217 a0001c0001t0012g0226 others(13): Show |
17 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.98-515T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645924 | |||||||
chr11:34645981 | C | T | 1 | a0001c0003t0077g0270 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.98-458C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34645981 | |||||||
chr11:34646027 | G | GGT | 8 | a0001c0001t0002g0173 a0001c0001t0002g0254 a0001c0001t0016g0379 others(5): Show |
10 | HG01074.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.98-373_98-372dupGT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34646027 | ||||||
chr11:34646027 | GGT | G | 85 | a0001c0001t0007g0049 a0001c0001t0008g0073 a0001c0001t0014g0188 others(82): Show |
90 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.98-373_98-372delGT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34646027 | ||||||
chr11:34646027 | GGTGT | G | 11 | a0001c0001t0002g0158 a0001c0001t0003g0306 a0001c0001t0014g0184 others(8): Show |
11 | HG01123.hp2 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-375_98-372delGT others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34646027 | ||||||
chr11:34646027 | GGTGTGT | G | 46 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0122 others(43): Show |
48 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.98-377_98-372delGT others(4): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34646027 | ||||||
chr11:34646027 | GGTGTGTG others(1): Show |
G | 110 | a0001c0001t0001g0016 a0001c0001t0001g0132 a0001c0001t0001g0143 others(107): Show |
120 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.98-379_98-372delGT others(6): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34646027 | ||||||
chr11:34646027 | GGTGTGTG others(3): Show |
G | 11 | a0001c0001t0001g0263 a0001c0001t0017g0017 a0001c0001t0017g0155 others(8): Show |
12 | HG00438.hp2 HG01496.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-381_98-372delGT others(8): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34646027 | ||||||
chr11:34646027 | GGTGTGTG others(7): Show |
G | 1 | a0001c0001t0001g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.98-385_98-372delGT others(12): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34646027 | ||||||
chr11:34646035 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.98-404T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34646035 | |||||||
chr11:34646062 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0007g0067 |
2 | HG00741.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.98-377G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34646062 | |||||||
chr11:34646101 | T | C | 1 | a0001c0001t0022g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.98-338T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | chr11 | 34646101 | |||||||
chr11:34646348 | G | GAT | 4 | a0001c0001t0035g0011 a0001c0001t0057g0178 a0001c0001t0062g0201 others(1): Show |
5 | HG02486.hp2 HG02622.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-88_98-87dupAT | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 34646348 | ||||||
chr11:34646693 | C | T | 1 | a0001c0001t0013g0307 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.343+9C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34646693 | |||||||
chr11:34646742 | A | C | 1 | a0001c0004t0052g0032 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.343+58A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34646742 | |||||||
chr11:34646790 | C | T | 1 | a0001c0001t0002g0300 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343+106C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34646790 | |||||||
chr11:34646852 | G | A | 1 | a0001c0001t0007g0097 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.343+168G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34646852 | |||||||
chr11:34646989 | T | C | 1 | a0001c0001t0014g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.343+305T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34646989 | |||||||
chr11:34647049 | A | C | 2 | a0001c0001t0012g0021 a0001c0001t0031g0179 |
3 | HG02257.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.343+365A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647049 | |||||||
chr11:34647054 | A | C | 7 | a0001c0001t0038g0200 a0001c0001t0047g0101 a0001c0001t0075g0195 others(4): Show |
8 | HG01891.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.343+370A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647054 | |||||||
chr11:34647083 | A | ACCC | 5 | a0001c0001t0004g0368 a0001c0001t0016g0219 a0001c0001t0016g0379 others(2): Show |
5 | HG02615.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+399_343+400ins others(3): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647083 | |||||||
chr11:34647084 | A | AC | 38 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0193 others(35): Show |
39 | HG00733.hp2 HG00735.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.343+408dupC | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 34647084 | ||||||
chr11:34647084 | A | ACC | 132 | a0001c0001t0001g0149 a0001c0001t0001g0165 a0001c0001t0001g0169 others(129): Show |
143 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.343+407_343+408dup others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 34647084 | ||||||
chr11:34647084 | A | C | 14 | a0001c0001t0003g0075 a0001c0001t0004g0368 a0001c0001t0014g0183 others(11): Show |
14 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.343+400A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647084 | |||||||
chr11:34647091 | CCA | C | 157 | a0001c0001t0001g0149 a0001c0001t0001g0169 a0001c0001t0001g0222 others(154): Show |
172 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.343+420_343+421del others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 34647091 | ||||||
chr11:34647093 | A | C | 206 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(203): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.343+409A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647093 | |||||||
chr11:34647095 | A | C | 132 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0118 others(129): Show |
145 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.343+411A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647095 | |||||||
chr11:34647097 | A | C | 2 | a0001c0001t0009g0069 a0001c0001t0010g0344 |
2 | HG02040.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.343+413A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647097 | |||||||
chr11:34647296 | T | G | 10 | a0001c0001t0001g0229 a0001c0001t0017g0017 a0001c0001t0017g0155 others(7): Show |
11 | HG01496.hp1 HG02615.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.343+612T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647296 | |||||||
chr11:34647404 | T | G | 5 | a0001c0002t0001g0207 a0001c0002t0004g0002 a0001c0002t0004g0206 others(2): Show |
8 | HG02132.hp2 NA18941.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.343+720T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647404 | |||||||
chr11:34647543 | C | A | 130 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0131 others(127): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.343+859C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647543 | |||||||
chr11:34647555 | T | C | 5 | a0001c0001t0013g0307 a0001c0001t0013g0309 a0001c0001t0013g0310 others(2): Show |
5 | HG01884.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+871T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647555 | |||||||
chr11:34647609 | G | A | 1 | a0001c0001t0007g0031 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.343+925G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647609 | |||||||
chr11:34647707 | A | T | 8 | a0001c0001t0016g0255 a0001c0001t0061g0198 a0001c0006t0013g0111 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.343+1023A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647707 | |||||||
chr11:34647844 | T | C | 4 | a0001c0003t0005g0014 a0001c0003t0005g0174 a0001c0003t0005g0190 others(1): Show |
5 | HG01891.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+1160T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34647844 | |||||||
chr11:34648278 | G | T | 1 | a0001c0001t0003g0319 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.344-741G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648278 | |||||||
chr11:34648346 | A | AAT | 22 | a0001c0001t0001g0143 a0001c0001t0002g0167 a0001c0001t0004g0368 others(19): Show |
23 | HG00738.hp1 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.344-655_344-654dup others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 34648346 | ||||||
chr11:34648346 | A | AATAT | 12 | a0001c0001t0014g0183 a0001c0001t0014g0188 a0001c0001t0016g0219 others(9): Show |
12 | HG02109.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.344-657_344-654dup others(4): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 34648346 | ||||||
chr11:34648346 | A | AATATAT | 8 | a0001c0001t0012g0217 a0001c0001t0012g0226 a0001c0001t0012g0367 others(5): Show |
8 | HG02258.hp1 HG02559.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.344-659_344-654dup others(6): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 34648346 | ||||||
chr11:34648346 | AAT | A | 6 | a0001c0001t0035g0011 a0001c0001t0057g0178 a0001c0001t0062g0201 others(3): Show |
7 | HG02486.hp2 HG02622.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.344-655_344-654del others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 34648346 | ||||||
chr11:34648405 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-614G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648405 | |||||||
chr11:34648406 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-613G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648406 | |||||||
chr11:34648411 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-608G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648411 | |||||||
chr11:34648417 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-602A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648417 | |||||||
chr11:34648423 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-596G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648423 | |||||||
chr11:34648486 | TTTATCCA others(4): Show |
T | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-531_344-521del others(11): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 34648486 | ||||||
chr11:34648517 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-502A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648517 | |||||||
chr11:34648521 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-498A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648521 | |||||||
chr11:34648522 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.344-497T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648522 | |||||||
chr11:34648716 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.344-303A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 3/8 | chr11 | 34648716 | |||||||
chr11:34649642 | C | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0239 a0001c0001t0001g0272 others(28): Show |
36 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.406+561C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34649642 | |||||||
chr11:34649722 | T | G | 1 | a0001c0002t0006g0335 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.406+641T>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34649722 | |||||||
chr11:34649807 | C | T | 1 | a0001c0001t0004g0368 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.406+726C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34649807 | |||||||
chr11:34650023 | T | C | 1 | a0001c0001t0014g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.406+942T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34650023 | |||||||
chr11:34650298 | A | C | 1 | a0001c0001t0001g0016 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.406+1217A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34650298 | |||||||
chr11:34650501 | G | A | 2 | a0001c0001t0002g0210 a0001c0001t0002g0240 |
2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.407-1041G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34650501 | |||||||
chr11:34650614 | G | A | 42 | a0001c0001t0001g0169 a0001c0001t0001g0229 a0001c0001t0002g0147 others(39): Show |
46 | HG00423.hp2 HG00735.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.407-928G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34650614 | |||||||
chr11:34650723 | G | A | 1 | a0001c0001t0016g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.407-819G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34650723 | |||||||
chr11:34650818 | G | A | 1 | a0001c0002t0023g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.407-724G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34650818 | |||||||
chr11:34651042 | T | A | 1 | a0001c0001t0003g0022 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.407-500T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651042 | |||||||
chr11:34651103 | C | T | 1 | a0001c0001t0007g0066 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.407-439C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651103 | |||||||
chr11:34651142 | TA | T | 147 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(144): Show |
162 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.407-397delA | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 34651142 | ||||||
chr11:34651150 | T | A | 147 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(144): Show |
162 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.407-392T>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651150 | |||||||
chr11:34651151 | C | T | 147 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(144): Show |
162 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.407-391C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651151 | |||||||
chr11:34651157 | C | A | 1 | a0001c0001t0061g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.407-385C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651157 | |||||||
chr11:34651342 | C | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(95): Show |
108 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.407-200C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651342 | |||||||
chr11:34651422 | G | T | 11 | a0001c0001t0013g0307 a0001c0001t0013g0309 a0001c0001t0013g0310 others(8): Show |
11 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.407-120G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651422 | |||||||
chr11:34651481 | G | A | 6 | a0001c0001t0014g0184 a0001c0001t0014g0187 a0001c0001t0014g0188 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-61G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651481 | |||||||
chr11:34651504 | AG | A | 163 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(160): Show |
178 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.407-37delG | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651504 | |||||||
chr11:34651506 | A | T | 163 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(160): Show |
178 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.407-36A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 4/8 | chr11 | 34651506 | |||||||
chr11:34651816 | A | G | 1 | a0001c0006t0037g0355 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.544+11A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34651816 | |||||||
chr11:34651888 | C | A | 1 | a0001c0001t0075g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.544+83C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34651888 | |||||||
chr11:34651898 | G | C | 1 | a0001c0001t0075g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.544+93G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34651898 | |||||||
chr11:34651973 | C | G | 12 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0149 others(9): Show |
12 | HG01106.hp1 HG01123.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.544+168C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34651973 | |||||||
chr11:34652227 | G | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(159): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.544+422G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34652227 | |||||||
chr11:34652337 | C | G | 93 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0013 others(90): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.544+532C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34652337 | |||||||
chr11:34652385 | G | C | 7 | a0001c0001t0017g0017 a0001c0001t0017g0155 a0001c0001t0017g0373 others(4): Show |
8 | HG01496.hp1 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.544+580G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34652385 | |||||||
chr11:34652421 | A | G | 1 | a0001c0001t0068g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.544+616A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34652421 | |||||||
chr11:34652706 | A | C | 1 | a0001c0002t0024g0340 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.544+901A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34652706 | |||||||
chr11:34652707 | AAG | A | 68 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0013 others(65): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.544+904_544+905del others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 34652707 | ||||||
chr11:34652850 | T | C | 1 | a0001c0001t0016g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.544+1045T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34652850 | |||||||
chr11:34652855 | C | G | 175 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(172): Show |
190 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.544+1050C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34652855 | |||||||
chr11:34652928 | G | A | 164 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(161): Show |
179 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.544+1123G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34652928 | |||||||
chr11:34652939 | G | A | 339 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(336): Show |
369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.544+1134G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34652939 | |||||||
chr11:34653058 | C | A | 1 | a0001c0001t0057g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.544+1253C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653058 | |||||||
chr11:34653140 | ACATCCTT others(1): Show |
A | 26 | a0001c0001t0013g0307 a0001c0001t0013g0309 a0001c0001t0013g0310 others(23): Show |
27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.544+1386_544+1393d others(10): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 34653140 | ||||||
chr11:34653140 | ACATCCTT others(9): Show |
A | 252 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(249): Show |
272 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(269): Show |
intron_variant | MODIFIER | c.544+1378_544+1393d others(18): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 34653140 | ||||||
chr11:34653140 | ACATCCTT others(17): Show |
A | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0013 others(93): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.544+1370_544+1393d others(26): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 34653140 | ||||||
chr11:34653313 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.544+1508A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653313 | |||||||
chr11:34653335 | C | G | 254 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(251): Show |
274 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(271): Show |
intron_variant | MODIFIER | c.544+1530C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653335 | |||||||
chr11:34653394 | T | C | 1 | a0001c0006t0037g0355 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.544+1589T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653394 | |||||||
chr11:34653400 | C | A | 1 | a0001c0001t0074g0223 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.544+1595C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653400 | |||||||
chr11:34653454 | C | T | 3 | a0001c0001t0036g0334 a0001c0001t0036g0365 a0001c0001t0065g0202 |
3 | HG02109.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.544+1649C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653454 | |||||||
chr11:34653464 | C | T | 1 | a0001c0002t0023g0257 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.544+1659C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653464 | |||||||
chr11:34653532 | C | T | 90 | a0001c0001t0004g0192 a0001c0001t0004g0368 a0001c0001t0006g0245 others(87): Show |
95 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.544+1727C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653532 | |||||||
chr11:34653663 | A | G | 1 | a0001c0003t0005g0141 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.544+1858A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653663 | |||||||
chr11:34653718 | A | T | 2 | a0001c0001t0002g0173 a0001c0001t0002g0254 |
2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.544+1913A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653718 | |||||||
chr11:34653959 | C | T | 1 | a0001c0001t0075g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.544+2154C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34653959 | |||||||
chr11:34654046 | C | T | 1 | a0001c0001t0028g0316 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.544+2241C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654046 | |||||||
chr11:34654169 | C | T | 1 | a0001c0002t0009g0041 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.544+2364C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654169 | |||||||
chr11:34654306 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.544+2501T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654306 | |||||||
chr11:34654380 | C | T | 1 | a0001c0001t0016g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.545-2528C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654380 | |||||||
chr11:34654390 | A | G | 1 | a0001c0002t0006g0296 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.545-2518A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654390 | |||||||
chr11:34654440 | C | T | 1 | a0001c0001t0069g0277 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.545-2468C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654440 | |||||||
chr11:34654441 | G | A | 1 | a0002c0005t0076g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.545-2467G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654441 | |||||||
chr11:34654448 | C | T | 1 | a0001c0001t0061g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.545-2460C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654448 | |||||||
chr11:34654568 | T | C | 1 | a0001c0002t0006g0234 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.545-2340T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654568 | |||||||
chr11:34654758 | C | T | 1 | a0001c0001t0016g0379 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.545-2150C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654758 | |||||||
chr11:34654971 | G | T | 1 | a0001c0003t0078g0186 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.545-1937G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34654971 | |||||||
chr11:34655035 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.545-1873T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655035 | |||||||
chr11:34655149 | A | C | 1 | a0001c0001t0017g0373 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.545-1759A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655149 | |||||||
chr11:34655260 | G | A | 1 | a0001c0006t0056g0305 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.545-1648G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655260 | |||||||
chr11:34655261 | C | A | 1 | a0001c0006t0056g0305 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.545-1647C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655261 | |||||||
chr11:34655295 | G | T | 69 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0013 others(66): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.545-1613G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655295 | |||||||
chr11:34655305 | G | A | 1 | a0001c0003t0011g0060 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.545-1603G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655305 | |||||||
chr11:34655417 | G | A | 2 | a0001c0003t0005g0377 a0001c0003t0011g0180 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.545-1491G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655417 | |||||||
chr11:34655469 | G | A | 1 | a0001c0001t0014g0184 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.545-1439G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655469 | |||||||
chr11:34655546 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.545-1362C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655546 | |||||||
chr11:34655813 | C | T | 72 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0013 others(69): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.545-1095C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655813 | |||||||
chr11:34655964 | A | C | 69 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0013 others(66): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.545-944A>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34655964 | |||||||
chr11:34656013 | A | T | 1 | a0001c0001t0036g0365 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.545-895A>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656013 | |||||||
chr11:34656053 | T | TAC | 3 | a0001c0001t0014g0187 a0001c0001t0016g0219 a0001c0001t0016g0255 |
3 | HG01109.hp2 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.545-831_545-830dup others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 34656053 | ||||||
chr11:34656053 | TAC | T | 337 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(334): Show |
367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.545-831_545-830del others(2): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 34656053 | ||||||
chr11:34656112 | G | A | 1 | a0002c0005t0005g0242 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.545-796G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656112 | |||||||
chr11:34656221 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.545-687T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656221 | |||||||
chr11:34656331 | G | C | 93 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(90): Show |
103 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.545-577G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656331 | |||||||
chr11:34656394 | TA | T | 46 | a0001c0001t0002g0172 a0001c0001t0007g0057 a0001c0001t0015g0358 others(43): Show |
50 | HG00423.hp2 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.545-502delA | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 34656394 | ||||||
chr11:34656497 | G | T | 3 | a0001c0001t0035g0011 a0001c0001t0057g0178 a0001c0001t0062g0201 |
4 | HG02486.hp2 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.545-411G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656497 | |||||||
chr11:34656570 | A | ACTTCTAT others(1): Show |
110 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(107): Show |
120 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.545-337_545-330dup others(8): Show |
EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 34656570 | ||||||
chr11:34656571 | C | T | 1 | a0001c0001t0012g0021 | 2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.545-337C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656571 | |||||||
chr11:34656591 | G | A | 1 | a0001c0002t0008g0052 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.545-317G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656591 | |||||||
chr11:34656671 | C | T | 1 | a0001c0001t0061g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.545-237C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656671 | |||||||
chr11:34656675 | T | C | 11 | a0001c0001t0016g0219 a0001c0001t0016g0379 a0001c0001t0019g0337 others(8): Show |
11 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.545-233T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656675 | |||||||
chr11:34656734 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.545-174A>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656734 | |||||||
chr11:34656809 | T | C | 3 | a0001c0001t0046g0112 a0001c0002t0034g0185 a0001c0002t0034g0230 |
3 | HG02257.hp1 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.545-99T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656809 | |||||||
chr11:34656886 | C | T | 44 | a0001c0003t0005g0014 a0001c0003t0005g0119 a0001c0003t0005g0141 others(41): Show |
48 | HG00423.hp2 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.545-22C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656886 | |||||||
chr11:34656888 | C | G | 362 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(359): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.545-20C>G | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 6/8 | chr11 | 34656888 | |||||||
chr11:34657255 | G | A | 338 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(335): Show |
368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.607+285G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657255 | |||||||
chr11:34657293 | G | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0239 a0001c0001t0001g0272 others(2): Show |
7 | HG00558.hp1 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.607+323G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657293 | |||||||
chr11:34657296 | G | A | 1 | a0001c0001t0061g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.607+326G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657296 | |||||||
chr11:34657345 | T | C | 15 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0149 others(12): Show |
15 | HG01106.hp1 HG01123.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.607+375T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657345 | |||||||
chr11:34657381 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(89): Show |
102 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.607+411G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657381 | |||||||
chr11:34657464 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.607+494G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657464 | |||||||
chr11:34657615 | C | A | 1 | a0001c0001t0032g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.607+645C>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657615 | |||||||
chr11:34657625 | CA | C | 373 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0117 others(370): Show |
404 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(401): Show |
intron_variant | MODIFIER | c.607+662delA | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 34657625 | ||||||
chr11:34657647 | G | A | 1 | a0001c0001t0003g0027 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.607+677G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657647 | |||||||
chr11:34657720 | G | T | 4 | a0001c0002t0023g0130 a0001c0002t0023g0135 a0001c0002t0023g0257 others(1): Show |
4 | HG01074.hp1 HG01952.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.607+750G>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657720 | |||||||
chr11:34657791 | GA | G | 7 | a0001c0001t0021g0104 a0001c0003t0005g0014 a0001c0003t0005g0174 others(4): Show |
8 | HG01891.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.608-730delA | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 34657791 | ||||||
chr11:34657906 | G | C | 1 | a0001c0001t0002g0158 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.608-627G>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34657906 | |||||||
chr11:34658266 | T | C | 1 | a0001c0001t0079g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.608-267T>C | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34658266 | |||||||
chr11:34658506 | G | A | 88 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.608-27G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 7/8 | chr11 | 34658506 | |||||||
chr11:34658767 | C | T | 15 | a0001c0001t0001g0117 a0001c0001t0001g0131 a0001c0001t0001g0153 others(12): Show |
16 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.803+39C>T | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 8/8 | chr11 | 34658767 | |||||||
chr11:34658803 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.804-29G>A | EHF | ENSG00000135373.13 | transcript | ENST00000257831.8 | protein_coding | 8/8 | chr11 | 34658803 |