Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region
Chrom. | Start | End | TF Name | Source | Predicted site? | Tissue/Cell line | id | More |
---|---|---|---|---|---|---|---|---|
chr19 | 52068856 | 52068861 | H4TF1 | TRANSFAC | yes | 70871954 | ||
chr19 | 52068885 | 52068902 | ESR1 | JASPAR | yes | 70871955 | ||
chr19 | 52068885 | 52068903 | ESR2 | JASPAR | yes | 70871956 | ||
chr19 | 52068886 | 52068901 | ESR2 | JASPAR | yes | 70871957 | ||
chr19 | 52068887 | 52068891 | H4TF2 | TRANSFAC | yes | 70871958 | ||
chr19 | 52068897 | 52068903 | SP1 | TRANSFAC | yes | 70871959 | ||
chr19 | 52068897 | 52068907 | SP1 | JASPAR | yes | 70871960 | ||
chr19 | 52068921 | 52068942 | ZNF263 | JASPAR | yes | 70871961 | ||
chr19 | 52068928 | 52068932 | NFE | TRANSFAC | yes | 70871962 | ||
chr19 | 52068931 | 52068937 | MZF1 | JASPAR | yes | 70871963 | ||
chr19 | 52068938 | 52068944 | ZNF354C | JASPAR | yes | 70871964 | ||
chr19 | 52068958 | 52068979 | ZNF263 | JASPAR | yes | 70871965 | ||
chr19 | 52068959 | 52068980 | ZNF263 | JASPAR | yes | 70871966 | ||
chr19 | 52068961 | 52068969 | EHF | JASPAR | yes | 70871967 | ||
chr19 | 52068962 | 52068983 | ZNF263 | JASPAR | yes | 70871968 | ||
chr19 | 52068987 | 52069000 | ZBTB18 | JASPAR | yes | 70871969 | ||
chr19 | 52068988 | 52068998 | NEUROG2 | JASPAR | yes | 70871970 | ||
chr19 | 52069007 | 52069022 | STAT1 | JASPAR | yes | 70871971 | ||
chr19 | 52069008 | 52069016 | EHF | JASPAR | yes | 70871972 | ||
chr19 | 52069009 | 52069020 | STAT3 | JASPAR | yes | 70871973 | ||
chr19 | 52069020 | 52069024 | NFE | TRANSFAC | yes | 70871974 | ||
chr19 | 52069020 | 52069025 | GATA1 | TRANSFAC | yes | 70871975 | ||
chr19 | 52069020 | 52069026 | GATA3 | JASPAR | yes | 70871976 | ||
chr19 | 52069024 | 52069039 | RUNX2 | JASPAR | yes | 70871977 | ||
chr19 | 52069026 | 52069044 | TP63 | JASPAR | yes | 70871978 | ||
chr19 | 52069027 | 52069038 | RUNX1 | JASPAR | yes | 70871979 | ||
chr19 | 52069028 | 52069038 | RUNX3 | JASPAR | yes | 70871980 | ||
chr19 | 52069029 | 52069038 | RUNX2 | JASPAR | yes | 70871981 | ||
chr19 | 52069040 | 52069055 | HNF4G | JASPAR | yes | 70871982 | ||
chr19 | 52069041 | 52069056 | HNF4A | JASPAR | yes | 70871983 | ||
chr19 | 52069054 | 52069065 | RUNX1 | JASPAR | yes | 70871984 | ||
chr19 | 52069055 | 52069065 | RUNX3 | JASPAR | yes | 70871985 | ||
chr19 | 52069056 | 52069065 | RUNX2 | JASPAR | yes | 70871986 | ||
chr19 | 52069095 | 52069110 | FOXP1 | JASPAR | yes | 70871987 | ||
chr19 | 52069098 | 52069106 | FOXO3 | JASPAR | yes | 70871988 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
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Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr19 | 51979838 | 51994206 | + | CEACAM18 | ENSG00000213822.5 | 51979838 | 1.0 | 1.0 | 17925 | 10985 | |
chr19 | 51994611 | 52005043 | - | SIGLEC12 | ENSG00000254521.2 | 52005043 | 0.99 | 1.0 | 17926 | 36190 | |
chr19 | 52022779 | 52035110 | - | SIGLEC6 | ENSG00000105492.11 | 52035110 | 0.99 | 1.0 | 17927 | 66257 | |
chr19 | 52074551 | 52092991 | + | ZNF175 | ENSG00000105497.3 | 52074551 | 0.76 | 0.99 | 17928 | 94568 | |
chr19 | 52095036 | 52097630 | - | AC018755.1 | ENSG00000167765.3 | 52097630 | 0.73 | 1.0 | 17929 | 71489 | |
chr19 | 52114781 | 52150151 | - | SIGLEC5 | ENSG00000105501.7 | 52150151 | 0.97 | 0.96 | 17930 | 18968 | |
chr19 | 52115344 | 52150142 | - | SIGLEC5 | ENSG00000268500.1 | 52150142 | 0.97 | 1.0 | 17931 | 18977 | |
chr19 | 52145806 | 52150054 | - | SIGLEC14 | ENSG00000254415.3 | 52150054 | 0.97 | 0.96 | 17932 | 19065 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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