EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-35306 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr9:127022960-127025800 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR1MA0112.3chr9:127025218-127025235TGGGTCATGTTGACCTG+6.11
ESR1MA0112.3chr9:127025218-127025235TGGGTCATGTTGACCTG-6.49
ESR2MA0258.2chr9:127025219-127025234GGGTCATGTTGACCT-6
EWSR1-FLI1MA0149.1chr9:127023893-127023911CCTGCCTGCCTTTTTTCC-6.43
TBX21MA0690.1chr9:127024112-127024122AAGGTGTGAA+6.02
TBX2MA0688.1chr9:127024112-127024123AAGGTGTGAAA+6.62
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_01861chr9:127019682-127026487Aorta
SE_02294chr9:127022788-127026561Astrocytes
SE_03002chr9:127022691-127023675Bladder
SE_03002chr9:127024662-127025261Bladder
SE_04593chr9:127022878-127025423Brain_Anterior_Caudate
SE_06625chr9:127020475-127024282Brain_Hippocampus_Middle
SE_09789chr9:127020459-127025650CD14
SE_23712chr9:127022911-127024213Colon_Crypt_1
SE_23712chr9:127025430-127026893Colon_Crypt_1
SE_24006chr9:127022943-127023583Colon_Crypt_2
SE_24006chr9:127023619-127024004Colon_Crypt_2
SE_26169chr9:127020544-127026534Duodenum_Smooth_Muscle
SE_27460chr9:127022771-127025031Esophagus
SE_29975chr9:127020517-127026913Fetal_Muscle
SE_31765chr9:127019634-127024311Gastric
SE_36996chr9:127017775-127027047HSMMtube
SE_38009chr9:127019560-127027254HUVEC
SE_38868chr9:127020328-127026820IMR90
SE_42506chr9:127018715-127025211Lung
SE_42506chr9:127025391-127027002Lung
SE_44293chr9:127020407-127025388NHDF-Ad
SE_44809chr9:127020406-127025436NHLF
SE_45648chr9:127018281-127031420Osteoblasts
SE_47283chr9:127020533-127027227Panc1
SE_47557chr9:127022859-127024103Pancreas
SE_47557chr9:127024547-127024960Pancreas
SE_49326chr9:127022858-127025095Right_Atrium
SE_50283chr9:127018364-127027003Sigmoid_Colon
SE_51779chr9:127022865-127024958Skeletal_Muscle_Myoblast
SE_52726chr9:127019757-127024667Small_Intestine
SE_54297chr9:127019137-127025287Spleen
SE_59258chr9:127016097-127031007Ly3
SE_60141chr9:127018983-127030974Ly4
SE_60448chr9:127019058-127056389DHL6
SE_63558chr9:127018230-127025190HSMM
SE_65907chr9:127020517-127023966Pancreatic_islets
SE_65907chr9:127025385-127027153Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9127023000127025489
chr9127023045127025795
Enhancer Sequence
TGAGCCACCA TGCCCGGCCA TGTCCCCATT TACTGAGGAT ATACTGTGTG CTAGGTCTGG 60
TGCTGTATTT TACCCAGTCC ACTCACCAAC ACTAAGATGG AAGCTGTCAC GATGCCCATT 120
TACAGATGAG GAAACTGGGG CACAGAGAGA TGAGAGAATG CGCCAAAGAC CATGTGCTAA 180
TACGCAGCAG AGCTGGATTT GAACCCAGGC TTGTCTGAGC AGAGCCCATG GTCTCCCCAC 240
TGTACTAGGA AGGTAGCAGG CACTGTGGGC TGGATGCCTG GCCTGTGCTG AGGTTCAGTG 300
TCGTTTTCCT GATCTTACAG AGAGGGAGGT TAAGTAACTT GGGCAGGGTC ATAAACCCAC 360
AAATGGCAGA GTCGGGATTC GAACCCATGT CTCTGATTCC AGAGTTCCTC ACCTTAAACC 420
ACATCTGGCT GCCTTTGTCG TGCTTTGCTC CTGTTGCATG CTGCAAAGCC AAGTAGGTTA 480
AGACAGGCTA GGTTCCTGCA GGGCTGGGTT GCCCGAGACC TGGGAGAGGT CTTCCAGAAG 540
GCACTGCTGG CCTTCCTCGC CCAGGGCCAG AGCTACTGGA GAGAAAGGGC TGCTGTTCAC 600
ATTTTTTCTT TTCTTTAAGT GCCCCAGATA CTTTTCATAA GGGAAGTGTC AAAACAATTG 660
TCAAAAGGAG AAGAATATTT CCTTCCTCTT CTCAGGCTAG ACCAAGCAAG GGAGTTGGAG 720
GGTGGAGAGT GGAGGGACCT GGTGAATCAT CCAAGATTAA ATACGGGCAG GCACTGCCAG 780
GCTTGTGTGG AGATGAGGCT GGGACACTGT TCGCAGGAAG AGTCCGGTGT TCTGGCCCCC 840
TGATGTCACC TTCACGGGCC TGACTCACAG TCCTAAATAT CTGACAGCGA GATCGCTTGT 900
AGGTAGGCTT CTTGTCACTT GTCATTTAAG TCCCCTGCCT GCCTTTTTTC CCTGCTCATT 960
TCCATTTCGA TCACGGCTTC TACTACATGT GCTTGAAATG AATGTTGTGT GTGAGGACCT 1020
GTGTGGTTTG GGCCATGTTG TGCCCCCCTG CCAGTGTCCT TCGGTGTTGA AAGGAAAAGG 1080
TATTTCTCTC CCTTCCATGT ATGTTCTGCA AATTGACGAA CATTTGCAAA TTGCTTTGAG 1140
ATGCGTTAAT TTAAGGTGTG AAATAATAGA TCTTGTGCGA AGGCTCAGCC ACATTTCTGG 1200
CATTGATGGA TTTTTCTCCC GTCTGGCCTG TGATTTGGGG AGGTAAAAAT AGTCCTTTTT 1260
TCCACATTTT TATCTTTTTT TTTTTTTGCT GACATCATTC TTAGGAAGTG GTGTGCACAT 1320
GCCGTGGAAC TTTACATGGA ACATGGAGCT CTGGGGAGCA GGAGTGCTCT TGGAGTGAGG 1380
GGTGGTCTGC GGTGGCCCAG GCACCCCCTG GCTGTCCGTG AAATGGCTTT GAAATGAGCA 1440
GGCACTGTTG AGGGCCTCAG TGGCTTTTTG GTATTTGGCT GTCTTTTCAC TTATGACTCT 1500
TGGGTAATGG CAAGATAACT TTTGGGGAAA ATGTTAGTTT AAAAAGAAAA AAAATCAGGC 1560
CAGCACTTTC ACTCATTCCT GTCTGAGCTG GTCCCTTCCT TTGGCCAAAG CTGAACTAAA 1620
CCAATGGCCT TCTCAGACTC GACTTCCAGA CAGAGGAGCC GACATTGGGG CAAATCAGTT 1680
GGTGGTGTAA TTTCCTGTGA TGTTAACTTT GGGAACTTGA ACTTGGAGTG GGAGCTAGCA 1740
TTTTGACATG TGTCCCTCTA ACAGGACTTG CTTGTGTGGA AACAGACCCC CACATACATG 1800
GCTGCGCCAT TGTCTCCAAT TCTGGATTTT TCCACAGATG ACTTCTCGGG TGATCTGGTG 1860
GTAAAGGCAC AGGTCTTCTA GCCAGGCCTT CTTGGCCTCC AGCAAGGGCA GGATCACAGC 1920
ACCCCACCAG ACCTGACTGG CCACCACCGC TGTAGCTGTG GCTGGGCGAG TGGGGGGGCC 1980
ATGGGAATTG AAAGATGGGG TGGCCGAGAT CTGAAATGCA TTCAGTTGCA GTGGCCTGGA 2040
TCTGCACGGA GCCGTTCTTT CTTTCTCTTA GACATCTGCA TGGTGGTGAC CTCATAGAAT 2100
TCTAAGAAAA AAGGGGCTTT ATGTAGGAAT TCCATAGAGT GTGAAGGAAT TTGGACAGGG 2160
GAAGGGGGAG GGAAGTTGCC ATTCAGAGCC TGCAGTGCCT GCATTTTCCC CGAATTGTTT 2220
AACCCTCATG CTTCAGAATT AGGCTGAGGC TTGCGGGGTG GGTCATGTTG ACCTGGGTGA 2280
ACAGAGATCC CTTTAAGAAG AACTTCTCCA TGTTCCAGAG GCGCGTTCTT ACTGCAGGTG 2340
AGTGGCAGTA TGGGAATTAG TCCACAGGCC CCTTCTCGAA TGCCTGCCCT CTCTTGTTCC 2400
TTGTCCTCAA CGTCTTTGAA ACTTGGGCTT GTTGGGAAGA CACCTGCAAA AGGATGGATG 2460
CACATGACCT TCAGCTCTAA TGAATCAAGC TGCTGATGAG GAATTCACTG GGCTCCCAAT 2520
CCAGAGAGCT TCGCACACAC CCACTGGGGT TGAGACGAGC ACTGGGTTTA TTTATTGTGG 2580
ACTTTTGGAG TCTGAAGGAC TCTTGCCACC CATCTGTTTC ACGGAACAGA ACCTGAGGCT 2640
CAGAGGGAGC AAGGCGCTCC CCCACAGCCG CATTGAGAGC CTGAGCCTGG GCACCCGATG 2700
GAGTGAATGA GGCTGGAGTC CCAGACCTGC CTCTCATGAG CACGTCGCCC ACTGAGCCTC 2760
AGCGTCATCA TCTGGAAAAC AGGGATAATA TTATGACCTC AGAAGCTTCG GGGGAGGAAG 2820
TAAGTGAAAT AATGCATTTC 2840