EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS191-12044 
Organism
Homo sapiens 
Tissue/cell
Trophoblast 
Coordinate
chr14:69417440-69420370 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr14:69417701-69417719CCTGCCTGCCCTCCTTGC-6.41
FOSL2MA0478.1chr14:69417913-69417924GGGTGACTCAG+6.02
Gata4MA0482.1chr14:69420142-69420153TCTTATCTCCC+6.62
JUNBMA0490.1chr14:69417913-69417924GGGTGACTCAG+6.02
ZBTB18MA0698.1chr14:69419154-69419167AAACATCTGGCTT-6.18
ZNF263MA0528.1chr14:69418085-69418106GAGTGAGGAGGGAGAGAAAGA+6.27
ZNF263MA0528.1chr14:69418088-69418109TGAGGAGGGAGAGAAAGAGGA+7.94
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00359chr14:69414459-69420814Adipose_Nuclei
SE_01544chr14:69417251-69420434Aorta
SE_02315chr14:69417362-69420547Astrocytes
SE_04266chr14:69417860-69419498Brain_Anterior_Caudate
SE_09473chr14:69411857-69420150CD14
SE_17458chr14:69417417-69420388CD4p_CD25-_CD45RAp_Naive
SE_22077chr14:69418807-69420476CD8_Naive_8pool
SE_24115chr14:69417535-69418879Colon_Crypt_2
SE_24115chr14:69418882-69419264Colon_Crypt_2
SE_24115chr14:69419958-69420263Colon_Crypt_2
SE_25810chr14:69417135-69420777Duodenum_Smooth_Muscle
SE_26589chr14:69417470-69420421Esophagus
SE_28065chr14:69417510-69420636Fetal_Intestine
SE_28974chr14:69417614-69420701Fetal_Intestine_Large
SE_31722chr14:69417476-69420402Gastric
SE_36138chr14:69404230-69420474HMEC
SE_37016chr14:69402168-69421041HSMMtube
SE_38329chr14:69415190-69420541HUVEC
SE_38873chr14:69417408-69420422IMR90
SE_42569chr14:69417379-69420396Lung
SE_45678chr14:69402257-69421189Osteoblasts
SE_47006chr14:69417563-69420364Ovary
SE_47970chr14:69417580-69417977Pancreas
SE_48719chr14:69417459-69420433Right_Atrium
SE_50146chr14:69417457-69420435Sigmoid_Colon
SE_52189chr14:69417379-69418877Skeletal_Muscle_Myoblast
SE_52189chr14:69419308-69420458Skeletal_Muscle_Myoblast
SE_52675chr14:69417467-69420545Small_Intestine
SE_53596chr14:69417436-69420443Spleen
SE_54485chr14:69401836-69420919Stomach_Smooth_Muscle
SE_57035chr14:69417503-69418707VACO_400
SE_64004chr14:69417435-69418987HSMM
SE_64004chr14:69419219-69420472HSMM
SE_65495chr14:69417210-69419260Pancreatic_islets
SE_65495chr14:69419417-69420709Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr146941752769420334
Number: 1             
IDChromosomeStartEnd
GH14I068931chr146939771969420516
Enhancer Sequence
GCTAATTTTT TGTATTTTTA GTAGAGACAT GGTTTCACTG TGTTAGCCAG GATGGTCTGG 60
ATCTACTGAC CTTGTGATCT GGCTGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG 120
AGCCACCACG TCCGGCCCTA AGCATGTCAA ACTTTTATCA TAAAACAAAA CAGATATTGA 180
AGACTTGTAA ATCAAAAACA TTTCAAATTG TGATTCAGGA GGGTGTTTAA GACCTCCAGT 240
TAGAGGGGGG CAATGTTATC ACCTGCCTGC CCTCCTTGCC ACCAGCACCA GCCTGCCTGC 300
AGAAGGCCAA GAAACTCTCC CAAGAAGCGA CGAAGGCAGA CGAACGGCAG GGCAGCTGGA 360
TAGCACAGGC CTTCCCTGGC CCCCCGCCCT TTGAGAAACA GTGGCAGGGA AGCGCCACCC 420
ATGGCCAGAG GCAACGGGGT GACGGGCAGG CTCCTCCCTG GGCCCTGACT CCAGGGTGAC 480
TCAGGCGCTG GTTTCCCCGG AAGGAAGTGA GCCAGCCGAC TCTCTTTTTC CCTTTCTAGG 540
AAGACACAAG GGAATGACTT GGCCCAATCC CAGGGGCCCA GCCTTTTTAC TCAGACTGTT 600
ATGGAGAAAC CACCCCACCG TCCTCCACTA CAGGAGAGGA AGCCAGAGTG AGGAGGGAGA 660
GAAAGAGGAA ACAGCTCATC CCACAGAGGA AGATACAGAA AAGGGGAGGC ACAATGGACA 720
AGACAGGGCC TTCTCTTTCT AACCTCAACT CCCAACATAA ATGCCCAAGG AGGGATGCAT 780
GGAAGCTCTG CAACCCCACA GACTTGGGCT CTGGTCCTGA CGTTCCCGCT GACTAGCTGT 840
GTGCCCTTGA CTCCGTTTCC CCAACTCTAA CGTGAAGGTG ATGCAACATT TGATATCCAA 900
GGCCCCTTTC AGCTCTGAAA CTCCAGGCTC CTGTAAAAGC CGGGTGATGG GCTGGGACTG 960
AGGAAGGCCT GGAGAAGACT GGACGTGGTC TTGGAACAGG GAGAGCTTTG GGTGTGGAGA 1020
CTCGTGCCTG GTACCCCTCC CAGAAGTAAT GGCTCTAAGT GCAGCACCAG TGTCCCCACC 1080
CTCAGGCCAA GTAACCCCAT CATTCATTCA CTCATTCATT CGTTCGTTCA TTCATTCAAG 1140
ATTTTCTAAA CTCTTACCCT GTGCCAGGTA CTATACTAAT GCTGGCAAAC AGCAGTGAAC 1200
AAGCGCAGCC TTGTGAACTT CCCATTGGGT CTGAAGATCT TTCACCCTAC TCCCTGTCCC 1260
CAGGGCCGGC CCTTTAAGGG AGTAGAGCAT GGAAGAGCAA AACAAACAGT AGCCAAAAGG 1320
GAAGCCACAT GAAGCTGGCA AAAGAGCAGT GAGCCAAGCT GAGAGCTGAG GGAGGTCTGG 1380
TTCAGTCTCC AGCTTTCCGG GCCTCAGTTT CTTTATCTGA CAGAGGGGGC TGGCTCTGGT 1440
TTCTGTGGGA CCTTCCAGCG CTGGTAGTCT AGACATCCTA GGGATTGACT CAACTTCTCA 1500
ATCCTGGGAT CGCCAGAGGG AGGCCTGCTG GAGGCCAGCC CTGGGCAGCT TCTGACAGGC 1560
CCCAGCTTGG ACTCCGCAGC AGCAATGACC CACCCGGGAC CCTGCGGGCT GCAGACAGGT 1620
CGAAGTGACA GGCGGCCAAC GGCAGGGAGT TCTGGGGCAC AAAGAATACA GCTTCAGCCT 1680
GGCAAAGTCC AGCTGCTGGA GGCTGCCTGA AAGCAAACAT CTGGCTTTAA CTGCAGAGAT 1740
AAAATGGATG TCACATGCAG TTTTCTCCAA GTTGTAACTG TCGGGCTTGG GATGGGGTCA 1800
AAGAATGAGA AGGAAGGTAG ATATGTGCCC TGTCCCTGTG CCGCAATGCC TAGTAGGGGA 1860
AAGCGGCATC CCGCCCACCC CCCATCCCTG CTGGATTTTA ACCATAAACA CAGCCCTTTT 1920
CTGAAGGCAC AGGCTTAACA CAAACCAGAT GCGGTAGGGA CTTTCCCCCA CCCCCTACCT 1980
TGGCCCTAAA ATTAAACGTT CAGTATCTTC TCTGCCAAAC CTCACTTGAA GGCCGAGCCT 2040
TAAAGAGCCA GAGCCTCCGG TTCTCACCCT CACACACTCT CAATCACATC TCCACTTAAA 2100
CAAAATGTCA AAGTCCCCCA AATGGAAAGT GTGGATGGAG CAGCCCCCAG GAGGGCCTGA 2160
CACCCAAGCA GGGCACGGGC AGATTTGAAA GGAGAAGGAA TGCTGATCCT CCACCACCAG 2220
TGACGCCACC AACCCAGAAG GGATGGAAAG GGTTTCCTGA GAGGGTCGGG GGGATGATTT 2280
CCCATCCCTA GGGGCATCTG CCACTGGAAC GCAGCCAACC CACAGGGAGT CAGCCTGCGC 2340
ACCCACCCCT GTCCCCAGGG GACTCTGGAG ATTCCTGGAA GAGCTTATTT CCTGGACTTC 2400
AGTTTCCAAT CTCTAGAAAA CAGGGTGAAT AACAGACATC TTATTTAACT CTGAGCTCAC 2460
TCACAGCTGT GATGATCTGA AAATCCCTCT TAGGCAAACT CAACTCTCCT GGTCTTCCTA 2520
GGTTTCCCCA ATGCCGGGCT GGTTGTTTCC CTGTCCTGAA AGCTCTCCTG GTCCTTCTTC 2580
CAGCCCCAGC TAAAGGCCCA AACCACTCCA CCCACTCCCT ACCCTCAGCC TCCATGTCCC 2640
CCACTCCATG CCTGAGCCAT GCATCAGCCT CAGCACTAAT CAGCGTGCCC AGCACAGGGA 2700
CATCTTATCT CCCCAGCAAA GACACATATC CTCTGCCCTT AAGCTCAGAG GACCACATCT 2760
TACACTGTGC GTACTCCGCA GAGCCTGGCA GTGCACAACA CACACTAAAG ATGCTCAAAG 2820
TGGGTCATTC AATCTCACCC AGTTGCCATG ACTCCTTAAG AAAAGGGACA AGTGACCAGG 2880
CACGGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCAGGC 2930