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

TagContent
EnhancerAtlas ID
HS101-00638 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr1:21645480-21646900 
Target genes
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXP1MA0481.2chr1:21646407-21646419TTCTGTTTACAC-6.22
Sox3MA0514.1chr1:21646519-21646529AAAACAAAGG-6.02
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00105chr1:21640019-21654616Adipose_Nuclei
SE_00854chr1:21642962-21648227Adrenal_Gland
SE_01643chr1:21642185-21648218Aorta
SE_02944chr1:21645843-21646528Bladder
SE_02944chr1:21646569-21647990Bladder
SE_04518chr1:21643279-21645748Brain_Anterior_Caudate
SE_04518chr1:21645844-21646711Brain_Anterior_Caudate
SE_05944chr1:21639044-21646536Brain_Hippocampus_Middle
SE_05944chr1:21646700-21650133Brain_Hippocampus_Middle
SE_08398chr1:21643228-21645720Brain_Inferior_Temporal_Lobe
SE_26127chr1:21642960-21646679Duodenum_Smooth_Muscle
SE_26770chr1:21642974-21647847Esophagus
SE_28486chr1:21644573-21646764Fetal_Intestine
SE_29337chr1:21644662-21646709Fetal_Intestine_Large
SE_31433chr1:21643029-21648183Gastric
SE_42174chr1:21642958-21646742Lung
SE_44380chr1:21642937-21647054NHDF-Ad
SE_45045chr1:21643168-21646698NHLF
SE_46660chr1:21643459-21645622Ovary
SE_46660chr1:21645855-21646940Ovary
SE_47592chr1:21643574-21645731Pancreas
SE_47592chr1:21645786-21646790Pancreas
SE_48583chr1:21642944-21648219Right_Atrium
SE_50108chr1:21643010-21645670Sigmoid_Colon
SE_50108chr1:21645842-21646761Sigmoid_Colon
SE_52633chr1:21642919-21645734Small_Intestine
SE_52633chr1:21645749-21646973Small_Intestine
SE_53334chr1:21642938-21645903Spleen
SE_54639chr1:21639148-21648300Stomach_Smooth_Muscle
SE_56171chr1:21645755-21646598u87
SE_65263chr1:21643359-21649820Pancreatic_islets
SE_67931chr1:21645755-21646598u87
SE_68932chr1:21643728-21645709H9
SE_68932chr1:21645866-21648182H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr12164572921645787
chr12164594921646849
chr12164592921646735
Number: 1             
IDChromosomeStartEnd
GH01I021312chr12163897321657659
Enhancer Sequence
GTTTTCAGTG GAGCTGGGTC TGTACAATCT CCCGGGCTCC GTTTTCTCAT CAGCTAAGTC 60
AAAATAATAA AGTGAGGCCA GGCACGGTGG CTCAAGCTCG TAATCCAAGC ACTTTGGGAA 120
GCCAAGGTGG GTGGATTGCC TGAGCTTAGG AGTTCGAGAC CAGCTTGGGC AACATGGTGA 180
AACCCCGTCT CCACTAAAAT ACAAAAAAGT AGCCAGGCGT GGTGGTGTGC GTCTATAATC 240
CCAGCTACTT GGGAGGCTGA GGTGGGACAA TCGCTTGAAC CCGGGAAGTG GAGGTTGCAG 300
TGAGCCGAGA TCGCATCACT GCTTTCCAGC CTGGGAGACA GAGCGAGACT CCGTCTCAAA 360
ATAATAATAA TCATAATCAT AATCATAATC ATAATCATAA AGTGGACTAC GCAGGGCTTT 420
TCTAGAGACA TGATAAGACC TCGTGTCTAA ATGGCCTGGT ACATACTAGG GCCTCCATAA 480
ATGCCGGCTC CATGCTGCCC CCACCTCTGT CCACCAGGGC ACCCCCGGCA CCAAGGGCCA 540
GACTCCCTCT GCTGCCCCCA ATCTGCTTCT CAGACTTTCT GCTCCTGGCC TTCCTGGGAG 600
CCCTCCAAGC CAGCAGCTGT GCCCTCCCCT CTGTGAACTG GGCAGGAAAG CCAGGCTCCA 660
TCCCTGTCCA ACTCTCCTCA GCCTCTCCTG AGACCTGGCT CCTCATTCTC GCCACTCCCT 720
ACCAGGCACC GGGAGGCACG GCTCACTGTT CCCTAGTTTG TCTTGGTCCC CCAGAGGGCC 780
AACAAGCAGT CTGGGTGTTT ACATTAGTTC AGCTGAGACA GGCTGAACAA ACACACGCGG 840
TCCCATGGCT TCTAGTGCCA GCCCCCACAC ACCACTCGCC ACCCAGGCTG TCTTGAGTCC 900
ACAGGTGTCC CCACCCCACT CCAGATCTTC TGTTTACACT CGGCAGCAGC GTCCCATCTT 960
TTGACTTCCC TGGGCCACAA TGTAAGAAAT ATTGTCTTGG GTCACACATA AAATACACCA 1020
ACGATAGCCG ATCAGCTAAA AAACAAAGGT GCATGCATAA ATCTCAGAAT GTTTTAAGAA 1080
AGTTTATGAA TCTGTGGTGA GCCGCATTCA AAGCCATCCC AGGTCACATG CGGCCCACGG 1140
GCCGCAGGTT GGACAAGCTC ATTCACAGAT TCTCCCCATG GATTCTGTTT GAGGTTTGCT 1200
GCGTCCAGCT GATACCTGGT GAGACACTAA CCCCGCCCAC GACTATCTCC AGGCTCCAGC 1260
CGTCAACAGC TGTATGGGCT CAAACAGGTC ACCGGACTTC TCATTTATAA AATGGGGATG 1320
GTGACAGGGC CAACCCCACA GAGGACTGCT ACGATCAAAT GGGATAATGA GAGGTAGGCG 1380
CTAAGCACGT TGCCTGCAGG GCTCATGGAA GGTGCTGGAG 1420