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
chr1 28269920 28269933 NR2F1 JASPAR yes 118260993
chr1 28269921 28269936 HNF4G JASPAR yes 118260994
chr1 28269921 28269936 NR2C2 JASPAR yes 118260995
chr1 28269922 28269936 NR2F1 JASPAR yes 118260996
chr1 28269922 28269936 RXRB JASPAR yes 118260997
chr1 28269922 28269936 RXRG JASPAR yes 118260998
chr1 28269922 28269937 HNF4A JASPAR yes 118260999
chr1 28269924 28269928 ESR1 TRANSFAC yes 118261000
chr1 28269924 28269936 INSM1 JASPAR yes 118261001
chr1 28269929 28269934 SP1 TRANSFAC yes 118261002
chr1 28269938 28269946 GATA3 JASPAR yes 118261003
chr1 28269951 28269955 NFE TRANSFAC yes 118261004
chr1 28269977 28269982 SP1 TRANSFAC yes 118261005
chr1 28269980 28269985 SP1 TRANSFAC yes 118261006
chr1 28269990 28269994 NFE TRANSFAC yes 118261007
chr1 28269991 28269996 GATA2 JASPAR yes 118261008
chr1 28270001 28270015 TCF7L2 JASPAR yes 118261009
chr1 28270001 28270016 LEF1 JASPAR yes 118261010
chr1 28270003 28270020 RXRA JASPAR yes 118261011
chr1 28270016 28270034 ESR1 JASPAR yes 118261012
chr1 28270025 28270044 REST JASPAR yes 118261013
chr1 28270042 28270054 INSM1 JASPAR yes 118261014
chr1 28270047 28270052 SP1 TRANSFAC yes 118261015
chr1 28270057 28270068 FOXC1 JASPAR yes 118261016
chr1 28270085 28270091 HiNF-A TRANSFAC yes 118261017
chr1 28270091 28270104 ELF1 JASPAR yes 118261018
chr1 28270094 28270100 PEA3 TRANSFAC yes 118261019
chr1 28270094 28270104 ETV6 JASPAR yes 118261020
chr1 28270094 28270105 ELK4 JASPAR yes 118261021
chr1 28270094 28270105 FLI1 JASPAR yes 118261022
chr1 28270095 28270103 EHF JASPAR yes 118261023
chr1 28270096 28270103 SPI1 JASPAR yes 118261024
chr1 28270117 28270130 JUN JASPAR yes 118261025
chr1 28270122 28270130 FEV JASPAR yes 118261026
chr1 28270155 28270169 SPIC JASPAR yes 118261027
chr1 28270163 28270178 HNF4G JASPAR yes 118261028
chr1 28270164 28270179 HNF4A JASPAR yes 118261029

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr1 28270046 rs12409437 T C
189107
chr1 28270047 rs543022052 T G
189108
chr1 28270155 rs114344773 G A
189109
chr1 28270190 rs79929012 C A no 189110
chr1 28270199 rs368324060 A G no 189111

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
chr1 28177085 28177255 - AL109927.1 ENSG00000268552.1 28177255 0.0 1.0 399 7342
chr1 28199055 28213196 + THEMIS2 ENSG00000130775.11 28199055 0.93 1.0 400 29142
chr1 28218035 28241257 - RPA2 ENSG00000117748.5 28241257 0.76 0.99 401 71344
chr1 28261504 28285668 + SMPDL3B ENSG00000130768.10 28261504 0.87 1.0 402 91591
chr1 28285973 28294607 + XKR8 ENSG00000158156.7 28285973 0.65 1.0 403 84236


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