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
chr16 89580011 89580021 ID4 JASPAR yes 49422274
chr16 89580011 89580021 TCF3 JASPAR yes 49422275
chr16 89580011 89580021 TCF4 JASPAR yes 49422276
chr16 89580012 89580021 SNAI2 JASPAR yes 49422277
chr16 89580013 89580018 USF2 TRANSFAC yes 49422278
chr16 89580080 89580095 TFAP2A JASPAR yes 49422279
chr16 89580080 89580095 TFAP2C JASPAR yes 49422280
chr16 89580083 89580094 EBF1 JASPAR yes 49422281
chr16 89580083 89580094 TFAP2A JASPAR yes 49422282
chr16 89580083 89580094 TFAP2B JASPAR yes 49422283
chr16 89580083 89580095 TFAP2A JASPAR yes 49422284
chr16 89580083 89580095 TFAP2B JASPAR yes 49422285
chr16 89580083 89580095 TFAP2C JASPAR yes 49422286
chr16 89580083 89580096 TFAP2A JASPAR yes 49422287
chr16 89580083 89580096 TFAP2B JASPAR yes 49422288
chr16 89580083 89580096 TFAP2C JASPAR yes 49422289
chr16 89580083 89580097 EBF1 JASPAR yes 49422290
chr16 89580083 89580097 ZIC1 JASPAR yes 49422291
chr16 89580084 89580093 TFAP2A JASPAR yes 49422292
chr16 89580084 89580097 TFAP2A JASPAR yes 49422293
chr16 89580084 89580097 TFAP2C JASPAR yes 49422294
chr16 89580085 89580096 EBF1 JASPAR yes 49422295
chr16 89580092 89580096 LFA1 TRANSFAC yes 49422296
chr16 89580117 89580125 TEAD3 JASPAR yes 49422297
chr16 89580124 89580130 TCF4 TRANSFAC yes 49422298
chr16 89580170 89580182 YY1 JASPAR yes 49422299
chr16 89580178 89580183 SP1 TRANSFAC yes 49422300
chr16 89580198 89580211 HSF2 JASPAR yes 49422301
chr16 89580201 89580212 STAT3 JASPAR yes 49422302
chr16 89580202 89580213 STAT3 JASPAR yes 49422303
chr16 89580212 89580222 ID4 JASPAR yes 49422304
chr16 89580212 89580222 TCF4 JASPAR yes 49422305
chr16 89580214 89580219 USF2 TRANSFAC yes 49422306
chr16 89580242 89580246 NFE TRANSFAC yes 49422307
chr16 89580248 89580266 NR3C1 JASPAR yes 49422308
chr16 89580251 89580266 PRDM1 JASPAR yes 49422309
chr16 89580251 89580266 STAT2 JASPAR yes 49422310

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr16 89580087 rs545558115 C G 4677681
chr16 89580108 rs563943808 A AGT no 4677682
chr16 89580109 rs543044924 C CAGCT no 4677683
chr16 89580127 rs141526994 T G
4677684
chr16 89580169 rs11310954 GT G no 4677685
chr16 89580169 rs398030126 GT G no 4677686

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
chr16 89334038 89556969 - ANKRD11 ENSG00000167522.10 89556969 0.74 1.0 15175 76977
chr16 89557325 89624176 + SPG7 ENSG00000197912.9 89557325 0.64 1.0 15177 77333
chr16 89627065 89630950 + RPL13 ENSG00000167526.9 89627065 0.73 1.0 15178 53205
chr16 89642176 89663654 + CPNE7 ENSG00000178773.10 89642176 0.86 1.0 15179 38094
chr16 89679716 89704839 + DPEP1 ENSG00000015413.5 89679716 0.97 0.99 15180 554


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