EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS024-07902 
Organism
Homo sapiens 
Tissue/cell
Cerebellum 
Coordinate
chr19:3382250-3383890 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr19:3383089-3383110GGAGCAGGGGTGAGGAGAGGA+6.85
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00151chr19:3381418-3385787Adipose_Nuclei
SE_00856chr19:3380840-3385570Adrenal_Gland
SE_01707chr19:3381454-3384168Aorta
SE_02932chr19:3381830-3382949Bladder
SE_02932chr19:3383227-3383928Bladder
SE_04083chr19:3382657-3384057Brain_Anterior_Caudate
SE_05012chr19:3381179-3384244Brain_Cingulate_Gyrus
SE_05799chr19:3380996-3384283Brain_Hippocampus_Middle
SE_06831chr19:3381480-3382657Brain_Hippocampus_Middle_150
SE_07968chr19:3381409-3385130Brain_Inferior_Temporal_Lobe
SE_08810chr19:3383138-3383473Brain_Mid_Frontal_Lobe
SE_26532chr19:3381400-3385656Esophagus
SE_31377chr19:3381268-3384107Gastric
SE_40606chr19:3381514-3384136Left_Ventricle
SE_41774chr19:3381422-3384037LNCaP
SE_42110chr19:3381324-3384151Lung
SE_44438chr19:3382696-3384062NHDF-Ad
SE_44948chr19:3382857-3383414NHLF
SE_44948chr19:3383447-3384073NHLF
SE_46637chr19:3381596-3383214Ovary
SE_46637chr19:3383293-3384028Ovary
SE_47452chr19:3381312-3382569Panc1
SE_47452chr19:3383051-3384234Panc1
SE_47457chr19:3382402-3382921Pancreas
SE_47457chr19:3383175-3383535Pancreas
SE_48051chr19:3380430-3391014Psoas_Muscle
SE_48561chr19:3381347-3384161Right_Atrium
SE_49442chr19:3383175-3384109Right_Ventricle
SE_50148chr19:3381398-3384151Sigmoid_Colon
SE_51098chr19:3381209-3391298Skeletal_Muscle
SE_53320chr19:3381240-3384047Spleen
SE_54509chr19:3381410-3391172Stomach_Smooth_Muscle
SE_65251chr19:3380964-3385902Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1933832653383637
Number: 2             
IDChromosomeStartEnd
GH19I003381chr1933813133382949
GH19I003382chr1933829553383972
Enhancer Sequence
GGTGGCCTGA GCGGAGCGGC CAGCGGGGAG GGTGTCTGAT GGTGGTGACA CGGGGCCAGG 60
AGGGCCTGAG GGAGGAGGCC AGTGCGTGTG GGTATGATGT GGTGGTCTGA GAGGGGAAGT 120
GGGCCTTGGA GAGTGCCCAA TGGGGGCGAC ACGGGGCACG GAGCATCTGA GGGAGGAGGC 180
TGGTGGGTAT AGATGTGATG TGGTGGTCTG AGAGGGGAGG CGAGTCTAGG AGAATATGTA 240
AAGTAGGTGA TATGGCACAA GGAGAGTCTG AGAGAGGAGG CCAGTGCATA TAGATGTGAT 300
GTGGTGGTCC AGGCAGGGCA GCAGGCCTGG GAGAGCATCT GATGGGGGTG ACATGGTGCA 360
AGGAGGGTCT GAGGGAGGAG GCTGGTGCGT GTAGATGTGA TGTGGTGGTC CAAGCGGGGA 420
GGCGGGCCTG GGAGAGCGTC TGACGCCGGG TGACACGGGG CAAGGAGGGT CTGAGGGAAG 480
AAGCCAGCAT GTGTAGATGT GATGTGGTGG TCTGAGGGGG GAGGCAGGCC TAGGAGAGCG 540
TCTAATGCAA GTGATATGGT GCAAGGAGCG TCTGAGGGAG GAGGCCAGTG CATGCAGGGC 600
CCAGGGTGGC TGCTGATGGG ATGTGGAGGT CAGATGGAGG AGGCAGGCCT AGCAGAGGTC 660
TCAAGTGAGA GATGGTACAA GGAGGTTTTT TTGACAGAGG AGGCAGGTGG GCTGTGGCGC 720
TCCAATGGTA GAGGCAGGAT CTCACCCTCA CGTCTGAGGG AGGAGGCAGG AAGGCCCTTG 780
AGGTCTCAGG GGGATGAGAA TGTCCTAGAT GGTCTTGGGC ACAACGGACG GCCTTGCTGG 840
GAGCAGGGGT GAGGAGAGGA GAGGGACAGG CCATCCCAGC CCTCCGAGGA GAGCCAAGAG 900
AGTCCTGGCA CCGCTTTCTG TGAATGCTTG TTGGTTGATT GACTCTCAGA CCATGCCAGC 960
AGAGGCCTGA TGAGCCTGGC CCTGCCAGAG GGGTGTTTGC CGGTGGTCAA ATGCCTGATG 1020
TTGAGACCAG CTAGCTCTGT GGGGTTGAGG AAATCCAAGG CGGCTTCCCA GAGGAGGAGG 1080
TGCAGCTGAG CTCAGCTCTG CAGGATGGCC AGGCCACAGT GAACAAGGAG ATGCCCCAGG 1140
GGTCCTGGCA GGAGCGTGGA GATGAGAGGC CTGATGCCTG TGCCTCTGGT CCCGGTGCTA 1200
AGAGCAGGGT TGGTCCTGCA GCTTCTTGGC TGCGTGGCCC TCTTGGACTT CAGTTTCTCT 1260
TGCCTGCCAA ATGGTGGAGA TGATCAGTCT GTAGCTGGAT GGGGCTATGG GAGGTTCCAG 1320
AAGATCATGC GTGTAGCCAC GTGCGAGGTG TCAGCTGCAT CCCAAGACCT GAGTGGGTGC 1380
ACAGCACACC CCTGCCATGC CCATCCAGGC CGTGTCTGGA GCACGCGTGA ACCCCCACAC 1440
ACCCAGGGGC TGCCAGAGCA TGTGGGATGG GTGTACGCCA GACGCAGACC CACACAGGTC 1500
ACCAGCCCAG CCCCAGCCCA GGCAGCACTC TATAGAAACA GGCAGTTGCA CAGCCTGAGA 1560
GGGAGGGGCA TTTGCCCGAA CAGGAGGACC CTGGGGCCAG ACTGCCCATG CTCCAGACAC 1620
AGCCCTTCTT TTCCCCAGCT 1640