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
chr11 10659957 10659964 NFATC2 JASPAR yes 37327794
chr11 10659957 10659964 NFATC2 JASPAR yes 114040578
chr11 10659989 10660010 ZNF263 JASPAR yes 37327795
chr11 10659989 10660010 ZNF263 JASPAR yes 114040579
chr11 10659990 10660001 E2F6 JASPAR yes 37327796
chr11 10659990 10660001 E2F6 JASPAR yes 114040580
chr11 10659996 10660006 GCM2 JASPAR yes 37327797
chr11 10659996 10660006 GCM2 JASPAR yes 114040581
chr11 10660007 10660016 THAP1 JASPAR yes 37327798
chr11 10660007 10660016 THAP1 JASPAR yes 114040582
chr11 10660010 10660014 LFA1 TRANSFAC yes 37327799
chr11 10660010 10660014 LFA1 TRANSFAC yes 114040583
chr11 10660021 10660040 RFX2 JASPAR yes 37327800
chr11 10660021 10660040 RFX2 JASPAR yes 114040584
chr11 10660024 10660028 NFE TRANSFAC yes 37327801
chr11 10660024 10660028 NFE TRANSFAC yes 114040585
chr11 10660025 10660041 RFX2 JASPAR yes 37327802
chr11 10660025 10660041 RFX3 JASPAR yes 37327803
chr11 10660025 10660041 RFX4 JASPAR yes 37327804
chr11 10660025 10660041 RFX5 JASPAR yes 37327805
chr11 10660025 10660041 RFX2 JASPAR yes 114040586
chr11 10660025 10660041 RFX3 JASPAR yes 114040587
chr11 10660025 10660041 RFX4 JASPAR yes 114040588
chr11 10660025 10660041 RFX5 JASPAR yes 114040589
chr11 10660041 10660045 H1TF2 TRANSFAC yes 37327806
chr11 10660041 10660045 NFE TRANSFAC yes 37327807
chr11 10660041 10660045 SRF TRANSFAC yes 37327808
chr11 10660041 10660045 H1TF2 TRANSFAC yes 114040590
chr11 10660041 10660045 NFE TRANSFAC yes 114040591
chr11 10660041 10660045 SRF TRANSFAC yes 114040592
chr11 10660043 10660053 NFATC3 JASPAR yes 37327809
chr11 10660043 10660053 NFATC3 JASPAR yes 114040593
chr11 10660050 10660065 AR JASPAR yes 37327810
chr11 10660050 10660065 AR JASPAR yes 114040594
chr11 10660064 10660084 TP53 JASPAR yes 37327811
chr11 10660064 10660084 TP53 JASPAR yes 114040595
chr11 10660067 10660085 TP53 JASPAR yes 37327812
chr11 10660067 10660085 TP53 JASPAR yes 114040596

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr11 10660045 rs113223907 A G 1842402
chr11 10660058 rs34068995 CTG C
1842403
chr11 10660058 rs397849192 CTG C
1842404
chr11 10660067 rs11603178 T G
1842405
chr11 10660074 rs147971557 C T
1842406

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand Gene Name Ensembl ID TSS TSI of Normal tissues TSI of Cancer tissues Distance between enhancer and TSS id More
chr11 10533225 10562777 - RNF141 ENSG00000110315.2 10562777 0.68 1.0 10574 2862
chr11 10578513 10633236 - LYVE1 ENSG00000133800.4 10633236 0.83 0.99 10575 73321
chr11 10594638 10715535 - MRVI1 ENSG00000072952.14 10715535 0.92 1.0 10576 44563


Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand miRNA Name miRBase ID TSS Score TSI of Normal tissues TSI of Cancer tissues id More

No results