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

TagContent
EnhancerAtlas ID
HS048-00028 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:1306930-1308110 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PLAG1MA0163.1chr1:1307190-1307204GGGGCCAAGGGGGG+6.93
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_32069chr1:1307023-1307693Gastric
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr113078841307984
Number: 1             
IDChromosomeStartEnd
GH01I001370chr113063491308210
Enhancer Sequence
GGACAGCTGA GGCACCGCCT CGCCGGGATG GTGACGTCTG GAGCAGGGGT ACCCACCGCT 60
GCTGACGTGA GCTGATGGGT TCGTCGTGGG GATGTCCTCA TGGTGCAGGG TGTGTGGCAG 120
CATCCCTGGC CTCCACCCAC CCATGCCAGT AGCACCTCCC ACTGACAACC ACAGATGTCT 180
CCAGATGCGG CTCAAAGCCA TGGTTGACCT GCCTCCCAGG AGCACCCCAA GCCGGCCCCC 240
ACGCAGGGGT GGAGGAGGCC GGGGCCAAGG GGGGTCCCAG GGCTGTGCCT GAGCTGGGTA 300
GGGCTGCTCC CCACCACGGG CTGCCCAGCT GAGCTCTGCA GGCTAGGACT CTGGACAGGT 360
CCACTCAGCT TCCCACATCT CCTCCCTCAT ACAGGGAAGG GGGAGGTGAG CCCGGGATGG 420
AAGGAAACGC GGGGGGGCAG CAGCACTACA GAGGGTGCCA GTGGTGGCCA AGAGCACCGG 480
GAGGCTGGGG CAGGGCCAGG CTTGGCACTG AGCGGGCTCC ACTTCACCTG GGAGAGTTTC 540
GGCCCTGGGA GCCCTGCCCC ACTCACAGCT GGGAAAACAG ACCCAGGAAT GATGCCTGTG 600
ACCCCAGCTG GGGCCCCACA AGACGCTTCC TGCCACCTGT CCTGGTCCCC AGCCCTGGAC 660
CCAGGAGCCC GGCTGCTGCC CCCCTGTGGT GGTCTGGGGA AGCGCACTTC CACCCGCTAC 720
AGCCTCCAGA CCCCTCCGTG CACTCAGGGA CCCACAGCCA AGGCCTACTG ACCTCGCTGG 780
CTGGCACGTC CAGGGCCCAA CTCCCAGGAC AATGTGTGAC CCACAAGTTC GTCCTGTTCT 840
AGAGAAACTG CTGGGAATAG CGCTCAAGTC CTCCCCAAGG TCTGATGGGC AAGGAACTCA 900
AGCTTGAGTC TCAGACACAT TTCTGTGACA AAAGACAAGA GGCCCCCACG TCTCTGGTGA 960
GAGGCAGCCC AGCCTTCAGC CTTCACACAC GGTGGGGGAG AGGCTGCGGC TCCAGAGCCT 1020
CCACTCAACC GCCTGGGGCG GACGCAAAGG CCCCTCTCCT GTCGCTGAGC TGTTGGGGGC 1080
AGCAGCTTCC CAGTGCCCAC CCATGCCCTG CTACCCAAGT CCAAGGGCCC CTGCACATCC 1140
CTGCTCTTAG GAATACCATG TTCCAGCCAG GCGCAGGGGC 1180