EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-17815 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr14:69417460-69420380 
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
GTAGAGACAT GGTTTCACTG TGTTAGCCAG GATGGTCTGG ATCTACTGAC CTTGTGATCT 60
GGCTGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACCACG TCCGGCCCTA 120
AGCATGTCAA ACTTTTATCA TAAAACAAAA CAGATATTGA AGACTTGTAA ATCAAAAACA 180
TTTCAAATTG TGATTCAGGA GGGTGTTTAA GACCTCCAGT TAGAGGGGGG CAATGTTATC 240
ACCTGCCTGC CCTCCTTGCC ACCAGCACCA GCCTGCCTGC AGAAGGCCAA GAAACTCTCC 300
CAAGAAGCGA CGAAGGCAGA CGAACGGCAG GGCAGCTGGA TAGCACAGGC CTTCCCTGGC 360
CCCCCGCCCT TTGAGAAACA GTGGCAGGGA AGCGCCACCC ATGGCCAGAG GCAACGGGGT 420
GACGGGCAGG CTCCTCCCTG GGCCCTGACT CCAGGGTGAC TCAGGCGCTG GTTTCCCCGG 480
AAGGAAGTGA GCCAGCCGAC TCTCTTTTTC CCTTTCTAGG AAGACACAAG GGAATGACTT 540
GGCCCAATCC CAGGGGCCCA GCCTTTTTAC TCAGACTGTT ATGGAGAAAC CACCCCACCG 600
TCCTCCACTA CAGGAGAGGA AGCCAGAGTG AGGAGGGAGA GAAAGAGGAA ACAGCTCATC 660
CCACAGAGGA AGATACAGAA AAGGGGAGGC ACAATGGACA AGACAGGGCC TTCTCTTTCT 720
AACCTCAACT CCCAACATAA ATGCCCAAGG AGGGATGCAT GGAAGCTCTG CAACCCCACA 780
GACTTGGGCT CTGGTCCTGA CGTTCCCGCT GACTAGCTGT GTGCCCTTGA CTCCGTTTCC 840
CCAACTCTAA CGTGAAGGTG ATGCAACATT TGATATCCAA GGCCCCTTTC AGCTCTGAAA 900
CTCCAGGCTC CTGTAAAAGC CGGGTGATGG GCTGGGACTG AGGAAGGCCT GGAGAAGACT 960
GGACGTGGTC TTGGAACAGG GAGAGCTTTG GGTGTGGAGA CTCGTGCCTG GTACCCCTCC 1020
CAGAAGTAAT GGCTCTAAGT GCAGCACCAG TGTCCCCACC CTCAGGCCAA GTAACCCCAT 1080
CATTCATTCA CTCATTCATT CGTTCGTTCA TTCATTCAAG ATTTTCTAAA CTCTTACCCT 1140
GTGCCAGGTA CTATACTAAT GCTGGCAAAC AGCAGTGAAC AAGCGCAGCC TTGTGAACTT 1200
CCCATTGGGT CTGAAGATCT TTCACCCTAC TCCCTGTCCC CAGGGCCGGC CCTTTAAGGG 1260
AGTAGAGCAT GGAAGAGCAA AACAAACAGT AGCCAAAAGG GAAGCCACAT GAAGCTGGCA 1320
AAAGAGCAGT GAGCCAAGCT GAGAGCTGAG GGAGGTCTGG TTCAGTCTCC AGCTTTCCGG 1380
GCCTCAGTTT CTTTATCTGA CAGAGGGGGC TGGCTCTGGT TTCTGTGGGA CCTTCCAGCG 1440
CTGGTAGTCT AGACATCCTA GGGATTGACT CAACTTCTCA ATCCTGGGAT CGCCAGAGGG 1500
AGGCCTGCTG GAGGCCAGCC CTGGGCAGCT TCTGACAGGC CCCAGCTTGG ACTCCGCAGC 1560
AGCAATGACC CACCCGGGAC CCTGCGGGCT GCAGACAGGT CGAAGTGACA GGCGGCCAAC 1620
GGCAGGGAGT TCTGGGGCAC AAAGAATACA GCTTCAGCCT GGCAAAGTCC AGCTGCTGGA 1680
GGCTGCCTGA AAGCAAACAT CTGGCTTTAA CTGCAGAGAT AAAATGGATG TCACATGCAG 1740
TTTTCTCCAA GTTGTAACTG TCGGGCTTGG GATGGGGTCA AAGAATGAGA AGGAAGGTAG 1800
ATATGTGCCC TGTCCCTGTG CCGCAATGCC TAGTAGGGGA AAGCGGCATC CCGCCCACCC 1860
CCCATCCCTG CTGGATTTTA ACCATAAACA CAGCCCTTTT CTGAAGGCAC AGGCTTAACA 1920
CAAACCAGAT GCGGTAGGGA CTTTCCCCCA CCCCCTACCT TGGCCCTAAA ATTAAACGTT 1980
CAGTATCTTC TCTGCCAAAC CTCACTTGAA GGCCGAGCCT TAAAGAGCCA GAGCCTCCGG 2040
TTCTCACCCT CACACACTCT CAATCACATC TCCACTTAAA CAAAATGTCA AAGTCCCCCA 2100
AATGGAAAGT GTGGATGGAG CAGCCCCCAG GAGGGCCTGA CACCCAAGCA GGGCACGGGC 2160
AGATTTGAAA GGAGAAGGAA TGCTGATCCT CCACCACCAG TGACGCCACC AACCCAGAAG 2220
GGATGGAAAG GGTTTCCTGA GAGGGTCGGG GGGATGATTT CCCATCCCTA GGGGCATCTG 2280
CCACTGGAAC GCAGCCAACC CACAGGGAGT CAGCCTGCGC ACCCACCCCT GTCCCCAGGG 2340
GACTCTGGAG ATTCCTGGAA GAGCTTATTT CCTGGACTTC AGTTTCCAAT CTCTAGAAAA 2400
CAGGGTGAAT AACAGACATC TTATTTAACT CTGAGCTCAC TCACAGCTGT GATGATCTGA 2460
AAATCCCTCT TAGGCAAACT CAACTCTCCT GGTCTTCCTA GGTTTCCCCA ATGCCGGGCT 2520
GGTTGTTTCC CTGTCCTGAA AGCTCTCCTG GTCCTTCTTC CAGCCCCAGC TAAAGGCCCA 2580
AACCACTCCA CCCACTCCCT ACCCTCAGCC TCCATGTCCC CCACTCCATG CCTGAGCCAT 2640
GCATCAGCCT CAGCACTAAT CAGCGTGCCC AGCACAGGGA CATCTTATCT CCCCAGCAAA 2700
GACACATATC CTCTGCCCTT AAGCTCAGAG GACCACATCT TACACTGTGC GTACTCCGCA 2760
GAGCCTGGCA GTGCACAACA CACACTAAAG ATGCTCAAAG TGGGTCATTC AATCTCACCC 2820
AGTTGCCATG ACTCCTTAAG AAAAGGGACA AGTGACCAGG CACGGTGGCT CACGCCTGTA 2880
ATCCCAGCAC TTTGGGAGGC CGAGGCAGGC AGATCATGAG 2920