EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-18769 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr3:183250020-183251200 
TF binding sites/motifs
Number: 16             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr3:183251056-183251074CTTTCCTTCCTTCCTTCC-10.53
EWSR1-FLI1MA0149.1chr3:183251060-183251078CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:183251036-183251054AGTTCTTTCCTTCCTTCC-6.74
EWSR1-FLI1MA0149.1chr3:183251068-183251086CCTTCCTTCCCTCTTTCT-6.94
EWSR1-FLI1MA0149.1chr3:183251120-183251138CCTTTCTTCCTTTCTTTC-7.02
EWSR1-FLI1MA0149.1chr3:183251116-183251134TCTTCCTTTCTTCCTTTC-7.18
EWSR1-FLI1MA0149.1chr3:183251064-183251082CCTTCCTTCCTTCCCTCT-7.85
EWSR1-FLI1MA0149.1chr3:183251040-183251058CTTTCCTTCCTTCCTTCT-8.46
EWSR1-FLI1MA0149.1chr3:183251052-183251070CCTTCTTTCCTTCCTTCC-9.09
EWSR1-FLI1MA0149.1chr3:183251048-183251066CCTTCCTTCTTTCCTTCC-9.17
EWSR1-FLI1MA0149.1chr3:183251044-183251062CCTTCCTTCCTTCTTTCC-9.47
ZNF263MA0528.1chr3:183251064-183251085CCTTCCTTCCTTCCCTCTTTC-6.22
ZNF263MA0528.1chr3:183251060-183251081CCTTCCTTCCTTCCTTCCCTC-6.24
ZNF263MA0528.1chr3:183251052-183251073CCTTCTTTCCTTCCTTCCTTC-6.45
ZNF263MA0528.1chr3:183251056-183251077CTTTCCTTCCTTCCTTCCTTC-6.48
ZNF263MA0528.1chr3:183251048-183251069CCTTCCTTCTTTCCTTCCTTC-6.93
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_09997chr3:183249806-183251117CD14
SE_11748chr3:183249851-183252447CD20
SE_13968chr3:183251026-183252057CD34_Primary_RO01536
SE_18732chr3:183251024-183252246CD4p_CD25-_Il17-_PMAstim_Th
SE_29421chr3:183249585-183252801Fetal_Intestine_Large
SE_43516chr3:183250140-183252725MM1S
SE_58323chr3:183220239-183279244Ly1
SE_60504chr3:183222014-183274594DHL6
SE_61518chr3:183220552-183274601Toledo
SE_62515chr3:183229386-183311073Tonsil
SE_67228chr3:183250140-183252725MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr3183250743183250943
Number: 1             
IDChromosomeStartEnd
GH03I183532chr3183249835183252580
Enhancer Sequence
CTGCTCACGC ACCGAGGAAA GGCCATGTGA GGACACAGTG AGAAGGTGGC CGTCTGCAAG 60
CCAGGAAGGG AGCCCTCACC AGAAACCAGA TCATGCTAGC AACTTGATGC TAGACTTCCA 120
GACTCTATAG AAGTGTGAGG AAATAAACAT TTCTGTTGTT TAAGCCACAT AGTCCATAGT 180
ATTTTGTTAT GGCAGCCCAA GCTGACTAAT ACTGGCAGTC TGTATCCACC CCAGACCCTT 240
GTAGTTCACA AACTAGCAAG GGCATTGATG CCCAAATAAC AGTCTACGAG GGGCCATAAG 300
AGACCTACAA AGTGCTGTGG AGGCCAAGAA TGGCTACTCA TAGAGAAGGA AAATTCTGAA 360
ATGTGAAGAT TATGGATAGG ATTTCTAGGT AACAAGCACA GTGAGTAAAG CCATAAAGAT 420
GCAAGGGCAT GAGGCATGAA GAGAAACTAG CAGACATGTG ATTCAGTTGA AGCTCAGGGG 480
ACAGGAGAGG GATGAAACAA TGGTCTGGAA AGATAACCTG GATCCTGCTT GTGGAGGGCA 540
CTGAAGGCAG GATAGGGAGT TAGGTTTTCA CTCAGTGAGC AATGGTGAGC CGTTGAAGGT 600
TGATGAGCAA AGGCAGGACT CAAAGAGAAC ATTTTAAGCA CATGTGTTCT CACTTTTGTT 660
TGCAGGTGAT GGGTGCCACT AGAGTCAAGT ATCAGATGAA CCCATAAAGA GCTGGGAGGC 720
TTGTGACAAT GTCAAAGCCT TTTCTCAGAA AATGTACTAA TTGAGGCAGT AGCCACACCG 780
CTAGGGAACA TCTCCAAACA TTAGTCACTG GACTTTCTAA GCTACAGACA CATGAACAGG 840
TTAGGGAGCC GTTATCTCCC AGCCAAGTCA CTGAAATGCA AAGGCCCTGG GTGGAGCTCT 900
GGTGATGTAA TTCCAAACGC TCGGACTTCC ATCTCAACAC GGAGGGGATT ACACCTCTAA 960
GTCCTGCCCC TCCTCTCTAT CCCACACTTC CTATTTATCT CTGGAAATCA ATCATCAGTT 1020
CTTTCCTTCC TTCCTTCTTT CCTTCCTTCC TTCCTTCCCT CTTTCTTTCT TCTTTCTTTC 1080
TCTCTTTTTC TTTGTTTCTT CCTTTCTTCC TTTCTTTCTC TTCCTTCTTT TCCTGGCCTC 1140
AAGTGACCCT CTTCCCTCAG GCTCCCCAGT AGCTAGGACT 1180