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

TagContent
EnhancerAtlas ID
HS120-00042 
Organism
Homo sapiens 
Tissue/cell
LNCaP-abl 
Coordinate
chr1:8229670-8230780 
Target genes
Number: 4             
NameEnsembl ID
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE40MA0464.2chr1:8229987-8229997ATCACGTGAC+6.02
LMX1BMA0703.2chr1:8230084-8230095AATTTAATTAA+6.32
MITFMA0620.2chr1:8229983-8230001AAAGATCACGTGACCACA+6.84
MITFMA0620.2chr1:8229983-8230001AAAGATCACGTGACCACA-6.84
TFEBMA0692.1chr1:8229987-8229997ATCACGTGAC+6.02
USF2MA0526.2chr1:8229985-8230001AGATCACGTGACCACA-6.53
ZNF263MA0528.1chr1:8229867-8229888AAAGGAGAGGGAAGAGAGAGA+6.14
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_33918chr1:8229333-8230616HCC1954
SE_34231chr1:8224429-8231079HCT-116
SE_47106chr1:8229101-8231021Panc1
SE_55963chr1:8229122-8230767u87
SE_65889chr1:8229106-8231055Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr182303708230423
Number: 1             
IDChromosomeStartEnd
GH01I008168chr182289158230994
Enhancer Sequence
TTTCCCCACC CCGACCCTGA AATTTCCCCC ATTTGTCTGA GCTATGGCCA CCTTACTGGC 60
TCAGAAGTCA GGCTACAATA CTGCAATGGA ACCGGGTGAT GAAGTGTCAT AAATAGTTAA 120
TACAAATTCT GCCAACAAGT TTGGGGTTAA TAGCCGATCT TAAAATGGGT AAGGGAAAGA 180
AAGGGAGAGG GAGGGAAAAA GGAGAGGGAA GAGAGAGAGA GACAAAGAAA AAGAGAGAGA 240
TTTTCTGGCA TTCATCCTAA GCATTTCAGC CGTAAACTGG TTTAGGCCAG TGAGACAGGA 300
TGTTCTGCAG AGCAAAGATC ACGTGACCAC ACAGTGCGAA CAAACAGATG GTGTATCATT 360
AACAAACTGC AACGCTGCAT TTCCTAGTCT CTCCAGGGTG TCAGTGACCC AGGCAATTTA 420
ATTAAAAACA TTAAAAAAAA AAAAAAAAGT GACAAGGGCC AAAGTTTCAT CCTGTTTAAA 480
TTCAACTTCA TCAAAAAAGT GGAGGGGCTA TCCCTTCCAT GAAACGTCCA CATATGAGCC 540
CCTCAGGGAA GTGGCACCAA CGTGTAGGTC AGTGGCACAG TCAGGCCTCT GGTCAGTGGC 600
CATTGATCCA GAAATGCGGC CAGGGCATGG CCAGGGCAGG GGCAGCTCCA GGACAGAGAC 660
CAGCTCGCCT CCCATTAGCC TCCTGGGGAG ACAGGACAGG TAAACAGCAG GGAGCTCAGG 720
GGGTTTTATG GACCAGGCCG TGTACACAGT TTGTCCCGAG TACAAACAAG CAGGTGGCCA 780
GTCTCACCTT TGTTCTAAGA AGCGGGATCC AGGCAGGCCA GGAGGCCCAG AGGGTAGCTG 840
TCAGGAGACA CTGGGGCCCA ACCAGGGCTT CCCACTGCAG GAGCGGGTCA GGAGCTTGGA 900
CACTCTCGGA CACTCAGCAC TGTCCTCGCT TGAACCTCCC CGGTAATGGC AGCATAAAGT 960
GATGGTCAAG GGGCATCCGG TTGGGACTCA AGAAGCTTAA TCCCAAATCC CTGCCCCACA 1020
GTCTACCAGT GACAGACACT GTGCTGAAGT CAGCCTCCAC ATGCTCACCT GTAGAATTGT 1080
GACAACATGG CAAGGGCAGG TGAAGGCCCC 1110