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

TagContent
EnhancerAtlas ID
HS116-00566 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr1:21663530-21666100 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6MA0677.1chr1:21665975-21665989TGACCTTTGAGCCT-6.37
RxraMA0512.2chr1:21665975-21665989TGACCTTTGAGCCT-6.14
ZNF263MA0528.1chr1:21664550-21664571CCCCTCTGCCCTCCCTCATCC-6.55
ZNF263MA0528.1chr1:21664532-21664553CCTTCCTTCCCCTTCTGCCCC-6.58
ZNF263MA0528.1chr1:21665441-21665462GGAGGAGGATGGGGAGAGGAG+8.11
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00105chr1:21656775-21671990Adipose_Nuclei
SE_00854chr1:21663168-21667245Adrenal_Gland
SE_01643chr1:21663301-21667219Aorta
SE_02944chr1:21664000-21666080Bladder
SE_03598chr1:21663453-21663971Brain_Angular_Gyrus
SE_04518chr1:21663353-21665909Brain_Anterior_Caudate
SE_05710chr1:21664624-21665800Brain_Cingulate_Gyrus
SE_05944chr1:21659989-21673592Brain_Hippocampus_Middle
SE_08398chr1:21663323-21665931Brain_Inferior_Temporal_Lobe
SE_26127chr1:21663680-21666771Duodenum_Smooth_Muscle
SE_26770chr1:21663415-21667226Esophagus
SE_28486chr1:21663392-21666819Fetal_Intestine
SE_29337chr1:21663370-21667087Fetal_Intestine_Large
SE_31433chr1:21663236-21672659Gastric
SE_39164chr1:21663441-21666942IMR90
SE_42174chr1:21663299-21667069Lung
SE_45045chr1:21663454-21666210NHLF
SE_46660chr1:21663525-21664021Ovary
SE_46660chr1:21664031-21667287Ovary
SE_47592chr1:21663572-21665292Pancreas
SE_47592chr1:21665303-21666898Pancreas
SE_48583chr1:21663300-21667219Right_Atrium
SE_50108chr1:21663357-21673470Sigmoid_Colon
SE_52633chr1:21663378-21667298Small_Intestine
SE_53334chr1:21663536-21666469Spleen
SE_54639chr1:21663094-21674002Stomach_Smooth_Muscle
SE_56171chr1:21663474-21665484u87
SE_65263chr1:21660486-21671744Pancreatic_islets
SE_67931chr1:21663474-21665484u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr12166399121664182
chr12166440021664833
chr12166494721665143
chr12166425521666064
Enhancer Sequence
AAAAAAACAA CAACAAAAAA AGAAAGTTAA ACACACATTG CCCCTCTGAC CCAGGAGTTG 60
CACTCCTAAG TATGTGCCCC AAAGAAATGA GTGCTGAGGT CTGCAAAGAG TTACATACGA 120
GAATGTCACA GCAGCCTCAA GCTGGAATCA ACCCAAATGT CAGCCACGGA CATTTACACG 180
TACATCCACC CAATGCGGCA CGACTCAGCC TAAAAAGGAG CAGATGCTGG TACAGGCGAC 240
ACGGACAAAC CTCAAACATT CCTTGCTGTC CAAAGCTGAA GAAAACCAGG CACAAAAGAG 300
CACACATGAA TGAATCCACA CAGAGAAAGC TCAAAACCAG GCCAAACTAG AGGGCCAGTG 360
GCCACCTGCT GCAGGGGACT GATGGAGGAG GCACACGGGA ACTGTGGGAA TGGTTCACAC 420
TTTGGTCCAG GTAGTATGCA GGTGTGTGCA TTTGTAAAAC GTGAGCTGTA CAAGATATGC 480
ATACATTACT TAAGTAAATT ATACTATACC ACAATTTTTA GAAACGTACA ATCTCTGCCC 540
TCATGAGGTC CAGTCTGGCA TCCTGTGTCA TCATCGTAAC AGTCATGACA ATAACAGCAG 600
GTGACACCGA CTGAGTCCTC TGTATGTGCC AGCCCTCAGC TGGGCTACTC TGAAACAGGA 660
TCTGATTGAG CGTTTCTAAC TACTGGGCAA AATACTGCCC CAGGAGCTCC ATATTAGAGA 720
CAGGAGAATA AAGCTTAGAG AGGTGACACG CTGTCCAAGG TGACAATGCA AAAAGTGAGG 780
ATGCCAGGTT TGAACCTGGG CCCATCAGTC TCCAAGGCCC ACTCCTGCTG CACGGGCAGA 840
TCCCGCCTCC CTGCCCTCTC CTCCCCACAC TGCCTGCTCA GATGTGGCAC CTGGAGGCAG 900
CCAGTCCTCG CCCCTCGCCC CCTCCTCTCC AGTGCTGGAA GGAACAGCTC ATGTGTGTAA 960
TGGACTCGAA GCTTCTGTGA AAGAGCTGCT GAGGAAATGA GTCCTTCCTT CCCCTTCTGC 1020
CCCCTCTGCC CTCCCTCATC CCTCTCATGG CCACATAGCT CTGAGGACAT TTCAGCCCTG 1080
GACCTCCGCC CAATAAGAAG GGACTCCAAT GGCCAGGCAG CTGGGGGTGT GTGTGGTATT 1140
GACCAAGGAG CTTTCTCAAC CCCTGGACAC CCCAGCCCAG CCTGTGGCCT CTCAGAGGAC 1200
CAGGAGGACA TGAGGTTAGA GTCCCCACCC TTGGCTCCAG TTTCCAAGTG ACGCAACCAA 1260
GTGTCTGGAT TCAGAGAATC GCAAAATGTT TATCTGGAAT CACAACCACC ACCATGACCA 1320
TTTAATCAAA CCTTATCCTG TGCCAAGTGC TACAAACATA GCTCATGAAT CCTCACCAGC 1380
AAACAAAATG GGTACTGCTA GGCTCTCATT TTACAGAGGA AGAAAGTGGA GCTCAAAGGG 1440
GTTAGGTGCC TTGCCCCAAG TCTCACAGTG AGGAAGTGGT GGGGCTGGAA TTCAAACCCA 1500
GATTTGCACA ACTTCGAGTC TATCCTCTGA ATGAGAGTAT TATACTTGTC ATCCTGCATG 1560
TCATTACTGA AGACGGCCCT GGAGTCAGTC TGCTCCAGCC ATGTCATTTC ACAGATGGGA 1620
AGACTGAGGC CCACGAAGGA AGACCGTGGT TCAGGAGGAC AAGGATTAGT GGCAGAGCCT 1680
GGGCTGGAAG CCACCCTGGC CTTGCTTTCA ATGACCAGAT CAGAGCCTGG GAGCGGGCCA 1740
TGTGCAGCTG GATGGGCAGC TGGAGGGAGT CAGGCAGGGA GGTGGGAGGC TCTGCTTCCA 1800
GGCAGAGGTA AATATTGACA TGACTGTGTT TACGCTGTAA CCTAACTCTG CCTGGCTGCT 1860
GCCCCAGGCC CACCCTCCTG CCTTCCCAGC CAAGGAGGGA AGGGAGCTGT GGGAGGAGGA 1920
TGGGGAGAGG AGGCTTCTGG GCCAGGGGCT GCTCCTCCTG CTTAGAGGGC TATGTGGTCA 1980
GAAAGGCTGG GACATCAGGT GTTAGGGGTG GGGGTTAGTG GAGACCCAGG CCAGGGGACC 2040
AGGTGGTGCC AGACAGGGAG GGGCTGTTAT CTGAGCTGGG GAGCTGGGGA TCTCAGGGCG 2100
GGGGACTGGG CTGGGAGTCA CAAGGCCTGA GTTCAAGTTC TAGTTCTGCT ACTGATTGGC 2160
AGTGGGAATC CAAGAACAGT CGGTGAATGG GGAAGAAAAG GTCTAACTGT CAAGTGCGGT 2220
GCAAAGGTGA ACAATAAATA ACCAGCATTT GAGCCTGGCC AGTGTCCAGC CCCAGTGAGC 2280
TCTCAACGCC TCTGGCTACC GGCTCAACAG TCCTATCCCT GTCCCAGTGG GCTTTCCCAG 2340
GAAGGCCAAG TTTCTGCCAA ACTGAGTGGC AGCTTGGGAC TGAAGCCATA ATAATCTAGA 2400
GGAATCGGGG AGCCACTGTC TAGCTCCCGT CCCTAATTCC CTAAGTGACC TTTGAGCCTC 2460
AGCTTTTACA ACTCTGAAAT AAGGCTCACC CTCCTCCCTG GGGTTGGTGT GAAGAGCAGA 2520
GATTACATTT AAGTGCCAGG CACATAGTAG ATGCTCATTT TGTCTCTCAG 2570