EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-23190 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr22:50326980-50329150 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr22:50329019-50329030GGGCGGGAAGG+6.62
FOSL2MA0478.1chr22:50328189-50328200GGGTGACTCAG+6.02
JUNBMA0490.1chr22:50328189-50328200GGGTGACTCAG+6.02
Klf1MA0493.1chr22:50328039-50328050AGGGTGTGGCC-6.32
ZNF263MA0528.1chr22:50329123-50329144CGAGGAGGTGGGGGGAGGGGA+6.07
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_03028chr22:50328039-50328938Bladder
SE_10057chr22:50326655-50329475CD14
SE_10530chr22:50326533-50329357CD19_Primary
SE_11301chr22:50322859-50332155CD20
SE_12420chr22:50327597-50329064CD3
SE_17545chr22:50326591-50331700CD4p_CD25-_CD45RAp_Naive
SE_17909chr22:50326643-50331570CD4p_CD25-_CD45ROp_Memory
SE_23129chr22:50326762-50329014Colon_Crypt_1
SE_23738chr22:50326901-50330921Colon_Crypt_2
SE_24687chr22:50326851-50332818Colon_Crypt_3
SE_26808chr22:50326694-50332325Esophagus
SE_28169chr22:50328251-50328925Fetal_Intestine
SE_31381chr22:50326539-50332985Gastric
SE_34375chr22:50326902-50329045HCT-116
SE_35007chr22:50326543-50329240HeLa
SE_42159chr22:50326486-50329239Lung
SE_47471chr22:50327181-50329026Pancreas
SE_49712chr22:50326718-50329026Right_Ventricle
SE_50117chr22:50326592-50329123Sigmoid_Colon
SE_52469chr22:50326640-50328989Small_Intestine
SE_53398chr22:50326561-50333542Spleen
SE_56937chr22:50327618-50330661VACO_400
SE_61206chr22:50315437-50364432HBL1
SE_61985chr22:50315627-50364432Toledo
SE_62450chr22:50318672-50364388Tonsil
SE_65335chr22:50326556-50329404Pancreatic_islets
SE_68380chr22:50327316-50364640TC32
SE_68381chr22:50327316-50364640TC32
SE_68382chr22:50327316-50364640TC32
SE_69071chr22:50328213-50329028H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr225032844250328844
chr225032765250328200
chr225032773050328489
chr225032721350327243
Enhancer Sequence
CCACCTCCAC AACCCCACGC AGCTCTGACC CTGGGCCCGC TCCAGCCCTG CAACTCATTA 60
GAGAGCTGCC TTCACAGCCA CTGATGGTCA AATGCTGCTG CCTGGCCATC ACCCCCGTCC 120
CTGTCAGCCA GTCCAGTGCT GTGACCGTCC CCTGCTCTCA GTTCCAGAGG ACAGCTGGGA 180
TCTGTGGTGC CACATGACTT TCAGCCCCTG TCTGCGGTGG CTGTTCTGAC ATTCACCCCT 240
CCTCACGTGT GTCCCACACT CCAGGAGCCT CTGGGCCGTG AAACAGAGCA GCAGAGGACA 300
CCGCCTCCTG GGGTCCTAGT CCTCAGAAAA GGGCCCACAA CCCGTCAGCT CTCCGCCGTC 360
CACCACATGC AGCTTATCTG GCTGGGCACG GCTTCGGGTC CCGGGCTCCT TCAGGCTGTG 420
GCCCCTTTGT CACTGGGCCA GCACATCCCC ACCAGGATAC ACTGCAACTT AATCCCAGGA 480
GGGTCTCGGG CAGGTCCTGG GTAATCCCAG GAGGGTCTCG GGCAGGTCCT GGGGAGCCGG 540
GGCAGGGGGC CGGCCTCTCC CACGGAGGAG GCACGGTTTG GAGACATCCT GTTTCTTCCC 600
AGCCAGCACC GAGGCCGGGG CACAGCAGAC CCCCGGGGAT GGGGTCACCT ATTGGTGGCC 660
CCTCTGGTCA CTGAGTCTGT GCGTGTTCTC CTGGCCTCTC CATGCAGCCT TCTGTTGTTT 720
TTCCAGAGCT TCAGGGGCGG GCACCAGCAG CCCCCCGAGG ACACTGTTCT CAAGGTTGTG 780
CCCCCTGGAC TCTCACCCCA GGCTCACCCA CCCCAAGAGT GCAGGCCCCT TCCCGTCGCG 840
TCCACCGCCA GTGGTGCCCG CTGGACAGAG TGCCTTTGCC TGTACACCTC CCTGGCGCTG 900
CCTGTCTGTG GCTGGCTCCA GAGTGGCAGG CGGTCTTGGC GCCTCAGCCA TGTCCTCAGC 960
TGACCTGGGG GCTGGGTGAG GTGAGGCACC CTGAGACTTC TTCAGCGTGC TGAGCTGTGA 1020
GGAGGGGGCT GGGCCTTTGG CCACCACAGG ATGACTCAAA GGGTGTGGCC TTCAGTGGGG 1080
TGCTCTCCTC AGCCTGCCCC TGCTGCTCCC TCAGCCCCCC GGTCCGGCTC TGTCCCTTTT 1140
CAGACTCCCA GACCCCGCAG GCCTGGGGTG GGGACTCTGC CTGCCACCTG GGAAGGGTGG 1200
TCGTCAGTGG GGTGACTCAG GGTGGAGGGC CCTGGCCCAG TGGCCCTGCC CTCCTCCTCA 1260
TATGCCCGTG ACCAGCACGC GGGTGTGGAC TGAGCCTGTG CCAGGTGGGC CCTGGGGGTC 1320
GGGGGGCAGA AGGGCCCAGG TCCTGCAGGG GAGTGGGGGG CGGTGCTGGG GCCCAGAAAG 1380
GCTTACTGTA ATGTGGCTGG TGGGGGCCAC CGGCTCTCAG GCCACACACT CCCCCTCCAG 1440
GCCCAGCGCC CCTCCCCGCC TCCCTGGGGC TGCGGTCTTC CCAAACCCCA AGCCGGCTGC 1500
TCTGCACCAG TGAGGGGCCG GGAGTGGCCT GGCCTGAGGA GGCTGCAGGG CACCCACCTC 1560
TCCAGAGACC CCCTCCACCC ACTCCCGGGG GATCCTTCTG GAGAGACCGT TCCCAGCCGT 1620
TGAGCAGGGT CCGCTCTCCC CCCTACCCCG GTCTGGCCTT TGGGAGGATC CCCCCAGAGC 1680
CAGGGAGGGG TATCTGGCCC CTCACCCCTC AAACGGCAGT CCAGGGCCAG CGTCTTTCTG 1740
CGCTCACCCA CCTGCCTGCG ACGGGGCTCT CTGGGCCACA GGGCGGCCAC CACTCGAGGG 1800
TCACCCGCAA GCCTCGGAGT CCCTGCTCGG AGCGGGGGCT GGTGGTCGCG GTGGGGGTGG 1860
GGAGCGGGCA CCCACTGGGG ATTCACCCCA CCCGGGCCCC CCTCCAGCCT CTGCCCGGCG 1920
CCCGGGTCTT CGGTCCGCCC TTTGCAGAGG AAGGACCCCG CCCTGCGCAG AGCGGGCTTG 1980
GGGGACCCGG GCGGGCGGCG GGGCGCGGGG TGGGGCGCGG GGGGCGGTGT TGCTCCCGCG 2040
GGCGGGAAGG GCGGGGAGCG GCCCTGCCGG GAAGGGGGCG GTGCCGGAAG CGTCAGCTGG 2100
GCTTTCCCCG GCGGGCGGGG GCGGGGAGCA GATGGGGGCG CTACGAGGAG GTGGGGGGAG 2160
GGGACGCAAT 2170