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

TagContent
EnhancerAtlas ID
HS040-01508 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr1:43413390-43414300 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MYCMA0147.3chr1:43414028-43414040GGGCACGTGGCT-6.18
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_01795chr1:43413274-43414277Aorta
SE_04284chr1:43412074-43414391Brain_Anterior_Caudate
SE_06192chr1:43411423-43414448Brain_Hippocampus_Middle
SE_08269chr1:43411549-43414442Brain_Inferior_Temporal_Lobe
SE_11009chr1:43387831-43425728CD20
SE_14471chr1:43395753-43414527CD4_Memory_Primary_7pool
SE_26580chr1:43413263-43414486Esophagus
SE_33837chr1:43413180-43413869HCC1954
SE_34353chr1:43413256-43414398HCT-116
SE_37191chr1:43404622-43414101HSMMtube
SE_41038chr1:43405665-43414583Left_Ventricle
SE_41620chr1:43413406-43414406LNCaP
SE_42796chr1:43411152-43414315Lung
SE_49782chr1:43413434-43414224Right_Ventricle
SE_58561chr1:43388242-43430420Ly1
SE_60624chr1:43388552-43428820DHL6
SE_62392chr1:43388423-43425814Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr14341372843413805
chr14341412643414217
Number: 1             
IDChromosomeStartEnd
GH01I042929chr14339554143414526
Enhancer Sequence
AAGGAATGGA ACCTGGGTCA TACCGTGTCT GCAGCCAGAG TGACGAGAGT AGGGAACAGC 60
ACATGCTAAT TGCCAAACAA AGAAACCTGC CACTTTTCAA TTTGGCTTTT GGGCAAAGCT 120
GGCTCTGTGA GTATCTGTTG TGCCAGACCA GTGTTCATCC TTAGCCATTT ATCAAACCCC 180
TGACGAGTGC TGGAACATCA GAGCTCTGAG AGGTAAATAC AGCACCCCAC AAAACCCTCC 240
ACTCCAAGCC CACAGGGCTG TCAAGGAAGG ACCTCTGAAG TCAGGCAGAC TGAGTTCAAA 300
TCCTGACTCT CCTAGGAGAG TCATGGCCTC CCAGCTTGGC CAGCAACTGG GCTCAGGGTC 360
CAGCACAGAG AAGCATTTCT CATGTCCCCA CCCCTCACCC TCCCTATCCC ACCGCTGGGG 420
GTCTCACGAC CCACAAGAGC CCTCCCTCTC CCAGGAAGCC ATGGATGAGG TGTTAAGATT 480
CAGGACCTCT CCCCCAACGC TCGGATGCCA GATGGCCCTG GCCACATTGT ATAACTTGCC 540
AAACACTGTG GCCTTTTGAC CCATGTCAGT GTGTCAGCAT TGCGCTCCAG CCCCAGGGTT 600
GGCCTGCAGC AGGTTCTCAA TCTATATTGG CACAGGAAGG GCACGTGGCT ACTGCTACTC 660
AGAGGCAGGG TATTCCTGGC AAGAGGAGGG TCCCAGGGCT GGCAGACTCC AGATGTTGCT 720
CCATCTTGTC CTCTTCCCAC AGCATCCCAC ATGGGTTCCC CAGGTGCAGG GAAGCAGGGG 780
ACGCAGGGCT TTCCAACTGC TTAGTCCACG GCTCAAAGGA GTGGGGGAGG GGTTTACCTG 840
AATCCATGAC AGCTCCCTTT TAATTTGTTT TGTTGTGTTT CTTACTCATT TAAATGAACT 900
TCTGGGCATT 910