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 |
---|---|---|---|---|---|---|---|---|
chr17 | 46767730 | 46767742 | IRF1 | JASPAR | yes | 21251092 | ||
chr17 | 46767730 | 46767744 | IRF7 | JASPAR | yes | 21251093 | ||
chr17 | 46767735 | 46767739 | YY1 | TRANSFAC | yes | 21251094 | ||
chr17 | 46767754 | 46767774 | TBX19 | JASPAR | yes | 21251095 | ||
chr17 | 46767756 | 46767772 | T | JASPAR | yes | 21251096 | ||
chr17 | 46767763 | 46767778 | FOXP1 | JASPAR | yes | 21251097 | ||
chr17 | 46767764 | 46767775 | HOXC12 | JASPAR | yes | 21251098 | ||
chr17 | 46767765 | 46767775 | HOXD11 | JASPAR | yes | 21251099 | ||
chr17 | 46767768 | 46767782 | STAT1 | JASPAR | yes | 21251100 | ||
chr17 | 46767768 | 46767783 | STAT2 | JASPAR | yes | 21251101 | ||
chr17 | 46767793 | 46767800 | POU2F1 | TRANSFAC | yes | 21251102 | ||
chr17 | 46767819 | 46767823 | H1TF2 | TRANSFAC | yes | 21251103 | ||
chr17 | 46767819 | 46767823 | NFE | TRANSFAC | yes | 21251104 | ||
chr17 | 46767819 | 46767823 | SRF | TRANSFAC | yes | 21251105 | ||
chr17 | 46767826 | 46767829 | MYB | TRANSFAC | yes | 21251106 | ||
chr17 | 46767831 | 46767842 | CEBPB | JASPAR | yes | 21251107 | ||
chr17 | 46767832 | 46767843 | CEBPA | JASPAR | yes | 21251108 | ||
chr17 | 46767872 | 46767877 | MYB | TRANSFAC | yes | 21251109 | ||
chr17 | 46767889 | 46767903 | PLAG1 | JASPAR | yes | 21251110 | ||
chr17 | 46767892 | 46767899 | SPIB | JASPAR | yes | 21251111 | ||
chr17 | 46767894 | 46767905 | EBF1 | JASPAR | yes | 21251112 | ||
chr17 | 46767899 | 46767904 | SP1 | TRANSFAC | yes | 21251113 | ||
chr17 | 46767918 | 46767923 | GATA2 | JASPAR | yes | 21251114 | ||
chr17 | 46767937 | 46767940 | MYB | TRANSFAC | yes | 21251115 | ||
chr17 | 46767940 | 46767944 | YY1 | TRANSFAC | yes | 21251116 | ||
chr17 | 46767940 | 46767955 | STAT1 | JASPAR | yes | 21251117 | ||
chr17 | 46767944 | 46767957 | HSF2 | JASPAR | yes | 21251118 | ||
chr17 | 46767946 | 46767956 | TEAD4 | JASPAR | yes | 21251119 | ||
chr17 | 46767947 | 46767955 | TEAD3 | JASPAR | yes | 21251120 | ||
chr17 | 46767949 | 46767960 | FOXA1 | JASPAR | yes | 21251121 | ||
chr17 | 46767949 | 46767964 | FOXA1 | JASPAR | yes | 21251122 | ||
chr17 | 46767950 | 46767961 | FOXB1 | JASPAR | yes | 21251123 | ||
chr17 | 46767950 | 46767961 | FOXC1 | JASPAR | yes | 21251124 | ||
chr17 | 46767950 | 46767962 | FOXC2 | JASPAR | yes | 21251125 | ||
chr17 | 46767961 | 46767979 | MAFF | JASPAR | yes | 21251126 | ||
chr17 | 46767963 | 46767978 | MAFK | JASPAR | yes | 21251127 | ||
chr17 | 46767966 | 46767977 | STAT3 | JASPAR | yes | 21251128 | ||
chr17 | 46767992 | 46768006 | CREB3L1 | JASPAR | yes | 21251129 | ||
chr17 | 46768026 | 46768031 | GATA2 | JASPAR | yes | 21251130 | ||
chr17 | 46768043 | 46768047 | ESR1 | TRANSFAC | yes | 21251131 | ||
chr17 | 46768060 | 46768073 | JUN | JASPAR | yes | 21251132 | ||
chr17 | 46768085 | 46768093 | FOXO3 | JASPAR | yes | 21251133 | ||
chr17 | 46768085 | 46768095 | NFATC3 | JASPAR | yes | 21251134 | ||
chr17 | 46768091 | 46768095 | YY1 | TRANSFAC | yes | 21251135 | ||
chr17 | 46768092 | 46768102 | HOXB13 | JASPAR | yes | 21251136 | ||
chr17 | 46768092 | 46768102 | HOXD13 | JASPAR | yes | 21251137 | ||
chr17 | 46768093 | 46768102 | CDX1 | JASPAR | yes | 21251138 | ||
chr17 | 46768093 | 46768104 | CDX2 | JASPAR | yes | 21251139 | ||
chr17 | 46768101 | 46768110 | THAP1 | JASPAR | yes | 21251140 | ||
chr17 | 46768101 | 46768112 | GCM1 | JASPAR | yes | 21251141 | ||
chr17 | 46768102 | 46768112 | GCM2 | JASPAR | yes | 21251142 | ||
chr17 | 46768108 | 46768112 | YY1 | TRANSFAC | yes | 21251143 | ||
chr17 | 46768108 | 46768121 | ELF1 | JASPAR | yes | 21251144 | ||
chr17 | 46768109 | 46768117 | FEV | JASPAR | yes | 21251145 | ||
chr17 | 46768117 | 46768121 | YY1 | TRANSFAC | yes | 21251146 | ||
chr17 | 46768118 | 46768126 | FEV | JASPAR | yes | 21251147 | ||
chr17 | 46768120 | 46768125 | ETS2 | TRANSFAC | yes | 21251148 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 46767999 | rs72831830 | C | T |
|
4911592 | |
chr17 | 46768065 | rs115314437 | C | T |
|
4911593 | |
chr17 | 46768085 | rs147859000 | A | G |
|
4911594 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr17 | 46626232 | 46682274 | - | HOXB3 | ENSG00000120093.7 | 46682274 | 0.96 | 1.0 | 15992 | 14549 | |
chr17 | 46668619 | 46671323 | - | HOXB5 | ENSG00000120075.5 | 46671323 | 0.95 | 1.0 | 15994 | 3598 | |
chr17 | 46671639 | 46682354 | - | HOXB6 | ENSG00000108511.8 | 46682354 | 0.99 | 1.0 | 15995 | 14629 | |
chr17 | 46684594 | 46710934 | - | HOXB7 | ENSG00000260027.3 | 46710934 | 0.95 | 1.0 | 15996 | 43209 | |
chr17 | 46688739 | 46692478 | - | HOXB8 | ENSG00000120068.5 | 46692478 | 0.99 | 1.0 | 15997 | 24753 | |
chr17 | 46698518 | 46703839 | - | HOXB9 | ENSG00000170689.8 | 46703839 | 0.99 | 1.0 | 15998 | 36114 | |
chr17 | 46799084 | 46799884 | - | PRAC1 | ENSG00000159182.3 | 46799884 | 1.0 | 1.0 | 15999 | 68242 | |
chr17 | 46802125 | 46806540 | - | HOXB13 | ENSG00000159184.7 | 46806540 | 0.98 | 0.98 | 16000 | 61586 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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