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

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EnhancerAtlas ID
HS048-14813 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr16:81437040-81437910 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CDX2MA0465.1chr16:81437292-81437303AGGCCATAAAA+6.02
CTCFMA0139.1chr16:81437304-81437323CGTCCAGCAGAGGGCGCCC+7.3
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr168143707281437212
Number: 1             
IDChromosomeStartEnd
GH16I081403chr168143677481441457
Enhancer Sequence
TATTGTGGGA TCAATGAATT CTAAATAAAA AATGCACTAA AAGTCTGTAG TGGGTGATGG 60
GGTGGGGGAT TTAGGGGTGC CGACGGGGTA GACCCCTATT GAAAGAGGCA CGAAAACTGG 120
GAGATGAAAA GCATAGGCTC GTTTGCCCTG TGTCTTCCTT CTCACGGCAG GGGATCGGCC 180
GGCCACCTTC TCCCTGTGAC TTCCTCCCAG TCCCGTCACC AAACCCCTGA GGCCGTCCTG 240
GCATCAGACC GCAGGCCATA AAAGCGTCCA GCAGAGGGCG CCCCAAACCC ACGAGGGCCG 300
CGGCGAAGAA GAAGGTAGCG GCCGCTGTCC TCTCCCCTCC CAGGCAGGTC CGGTGCGGAA 360
GGGATCGCTG GACACTGGCG ATGGTGGAGA GGCATGGTGG GCCGGGTCCC CCGCACCCTT 420
CATGGCCCTG ACTCGGGGCT GCCCATGACC TTCAGCGTCA GAGCTCGGTC TGGTCCATGC 480
CTGCCTTGGG GAAGCTGCGC CGCCTCTGCA CCCACCCAGG TCAGGGCCAC CTTCCCTCCA 540
TTTGCAGCAT GAGCAGGTCT GAGGTGGCGG CTCCGGGCTG AACAGCAGGA ACTGAGTTCT 600
TTGTCCACAT GTGAGGGTGG GCAGCCCATG AACAGTCCAC CCAGACACAA GTTACCCTGC 660
CCCCGAGCCG GAATCCAGCC CTGAGACCCC ACAGTGCTGC CTCTGAAACA GTGCTGGGAC 720
GTCTCTCTGA GCCTGAGCTC AGACTTTGGT GTCCCGCTGC TGAGGCCGGG GTCCCGCCGC 780
TGTGACCGTG GCAAGGGTAA GCCCTTTGTG CACCTGTGCC GTTGCCTGTA AAATGCTGGC 840
AGTAATCACA GTGGAGCTAC CCTAGAGGTT 870