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
chr7 98749979 98749994 FOXP1 JASPAR yes 26101832
chr7 98749980 98750001 IRF1 JASPAR yes 26101833
chr7 98749981 98749996 FOXP1 JASPAR yes 26101834
chr7 98749981 98750002 IRF1 JASPAR yes 26101835
chr7 98749982 98750003 IRF1 JASPAR yes 26101836
chr7 98749986 98750001 PRDM1 JASPAR yes 26101837
chr7 98749986 98750007 IRF1 JASPAR yes 26101838
chr7 98749987 98750002 FOXP1 JASPAR yes 26101839
chr7 98749988 98750009 IRF1 JASPAR yes 26101840
chr7 98749989 98750003 IRF7 JASPAR yes 26101841
chr7 98749992 98750007 FOXP1 JASPAR yes 26101842
chr7 98749994 98750015 IRF1 JASPAR yes 26101843
chr7 98749995 98750016 IRF1 JASPAR yes 26101844
chr7 98749998 98750012 SPIC JASPAR yes 26101845
chr7 98749999 98750013 SPIC JASPAR yes 26101846
chr7 98749999 98750013 STAT1 JASPAR yes 26101847
chr7 98749999 98750014 PRDM1 JASPAR yes 26101848
chr7 98749999 98750014 STAT2 JASPAR yes 26101849
chr7 98750001 98750022 IRF1 JASPAR yes 26101850
chr7 98750003 98750008 ETS2 TRANSFAC yes 26101851
chr7 98750005 98750020 PRDM1 JASPAR yes 26101852
chr7 98750005 98750020 STAT2 JASPAR yes 26101853
chr7 98750005 98750026 IRF1 JASPAR yes 26101854
chr7 98750006 98750021 FOXP1 JASPAR yes 26101855
chr7 98750006 98750027 IRF1 JASPAR yes 26101856
chr7 98750007 98750028 IRF1 JASPAR yes 26101857
chr7 98750008 98750022 IRF7 JASPAR yes 26101858
chr7 98750011 98750026 FOXP1 JASPAR yes 26101859
chr7 98750011 98750032 IRF1 JASPAR yes 26101860
chr7 98750012 98750027 FOXP1 JASPAR yes 26101861
chr7 98750012 98750033 IRF1 JASPAR yes 26101862
chr7 98750013 98750028 FOXP1 JASPAR yes 26101863
chr7 98750016 98750031 PRDM1 JASPAR yes 26101864
chr7 98750016 98750031 STAT2 JASPAR yes 26101865
chr7 98750018 98750039 IRF1 JASPAR yes 26101866
chr7 98750021 98750035 IRF7 JASPAR yes 26101867
chr7 98750022 98750037 PRDM1 JASPAR yes 26101868
chr7 98750023 98750035 IRF1 JASPAR yes 26101869
chr7 98750030 98750044 SPI1 JASPAR yes 26101870
chr7 98750030 98750044 SPIC JASPAR yes 26101871
chr7 98750045 98750049 H4TF2 TRANSFAC yes 26101872
chr7 98750060 98750075 PRDM1 JASPAR yes 26101873
chr7 98750090 98750095 GATA2 JASPAR yes 26101874
chr7 98750096 98750100 LFA1 TRANSFAC yes 26101875
chr7 98750102 98750108 SOX10 JASPAR yes 26101876
chr7 98750107 98750112 ETS2 TRANSFAC yes 26101877
chr7 98750115 98750123 E2F1 JASPAR yes 26101878
chr7 98750118 98750123 SP1 TRANSFAC yes 26101879
chr7 98750122 98750139 RXRA JASPAR yes 26101880
chr7 98750141 98750147 ETS1 JASPAR yes 26101881
chr7 98750148 98750151 MYB TRANSFAC yes 26101882
chr7 98750153 98750165 FOXI1 JASPAR yes 26101883
chr7 98750173 98750181 GATA3 JASPAR yes 26101884
chr7 98750176 98750186 SMAD3 JASPAR yes 26101885
chr7 98750198 98750213 HNF1A JASPAR yes 26101886
chr7 98750199 98750212 HNF1B JASPAR yes 26101887
chr7 98750200 98750212 HNF1B JASPAR yes 26101888
chr7 98750202 98750218 SOX8 JASPAR yes 26101889
chr7 98750208 98750211 MYB TRANSFAC yes 26101890
chr7 98750209 98750219 MYF6 JASPAR yes 26101891
chr7 98750225 98750239 NR2F1 JASPAR yes 26101892
chr7 98750234 98750238 H1TF2 TRANSFAC yes 26101893
chr7 98750234 98750238 NFE TRANSFAC yes 26101894
chr7 98750234 98750238 SRF TRANSFAC yes 26101895
chr7 98750234 98750248 POU1F1 JASPAR yes 26101896
chr7 98750235 98750247 POU3F1 JASPAR yes 26101897
chr7 98750235 98750247 POU3F2 JASPAR yes 26101898
chr7 98750235 98750248 POU3F3 JASPAR yes 26101899
chr7 98750236 98750247 FOXB1 JASPAR yes 26101900
chr7 98750236 98750248 POU2F1 JASPAR yes 26101901
chr7 98750237 98750246 POU5F1B JASPAR yes 26101902
chr7 98750255 98750271 RFX2 JASPAR yes 26101903
chr7 98750255 98750271 RFX3 JASPAR yes 26101904
chr7 98750255 98750271 RFX4 JASPAR yes 26101905
chr7 98750255 98750271 RFX5 JASPAR yes 26101906
chr7 98750256 98750261 GATA1 TRANSFAC yes 26101907
chr7 98750266 98750269 MYB TRANSFAC yes 26101908
chr7 98750272 98750276 YY1 TRANSFAC yes 26101909
chr7 98750272 98750287 STAT1 JASPAR yes 26101910

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr7 98749980 rs35293467 C CA
9976950
chr7 98750058 rs545589408 C A no 9976951
chr7 98750105 rs143206880 A G
9976952
chr7 98750185 rs9691980 C T
9976953

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
chr7 98625061 98741723 - SMURF1 ENSG00000198742.5 98741723 0.71 1.0 7620 91745
chr7 98771197 98805129 - KPNA7 ENSG00000185467.7 98805129 0.89 1.0 7621 45173


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