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

TagContent
EnhancerAtlas ID
HS073-09487 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr21:34785160-34786190 
Target genes
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF1AMA0046.2chr21:34785339-34785354GGTTAATTATTAGCT-6.19
HNF1BMA0153.2chr21:34785340-34785353GTTAATTATTAGC-6.12
MecomMA0029.1chr21:34785170-34785184TTCTATCTTGTCTC-6
RARA(var.2)MA0730.1chr21:34785649-34785666AGGTCACCCAGAGCTCA+6.66
TCF7L2MA0523.1chr21:34785307-34785321TGGCTTTGATGTCT-6.05
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_00219chr21:34785232-34786512Adipose_Nuclei
SE_10924chr21:34771599-34789021CD20
SE_53174chr21:34783007-34786227Small_Intestine
SE_53413chr21:34785125-34786015Spleen
SE_58466chr21:34731200-34786233Ly1
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr213478524034786016
Number: 1             
IDChromosomeStartEnd
GH21I033410chr213478269634787496
Enhancer Sequence
AGGAGTTTAT TTCTATCTTG TCTCATTTAC AGTTTGGTCC GGAGAGCTGC CTTAGACTCT 60
CCAATAAATC TATTCAAACA GCTGCCTCTG TTATCTTGAC TTGCTCCAGG TTTGGAAGAA 120
GCCTGTGTAG GATCTGTGTT TCATTTCTGG CTTTGATGTC TGGGCGTCAG TTTCCCTGGG 180
GTTAATTATT AGCTTAATGT GAAGGCAGCA TTGTGGAAAT TTCTCTGCAT AGTTCGGATG 240
CTATTCAGAT CTGTCTGTGT GACTGTCATG CAGGCCTCTC TGTGTGACTG TGAGGGAGCA 300
TTGACCTGCC ACCACCCCCC TCTGGAAGCA TCCAGTCCCC AACTGGCTTT GGGCATTGCT 360
AGGTCATAGC AGCCACAGCA CACCTGGTGG GCCTGCCTCT TGCCACGCAG CTTTACCTGT 420
CTGCCTTCGG CCCAGGATGT CATGAGGCCT GCTGTGTGTC AGGAGAAGTG TTGTTAGCTG 480
GTTGGGTGAA GGTCACCCAG AGCTCATAGG TGTGGAGGGG AGGGGCATCC TATAACTAAA 540
CAAATGGCCG CAGACTTGGC AATTCATCTT TCAGAAGAAG AGCCAGTGGT CAGGCTGTCA 600
GCTGATCTCT TTGAGGTTGA GCGCATTTAC CGAAAATGTG TGGCTTGAAT TTCCTGCTTT 660
GAATTTTGGA ACAGCATGTT TTTCAAACCT TTCTTCCACC TTCTGGGCAT TTCTTATTAA 720
TCTTTTTGGT CAAAAGCCTT ATCTTGATTA TGTTTTCTTT CTAAGACAAA GGGCTCCCTG 780
TGAAGTACCT GCTTGGGAAA GGGAGGAGTT GTGGCAGTTT CTTCTAGGTC CCCGAAGGCT 840
CCCTGTGAAG TACCTGCTTG GGGAAGGGAG AGGTTGTGGT TGTTTCTTCC AGGTCACCCC 900
AAAGAGAGGG ATTCTGATAT TGGTGGTGTT TCCGGGGGAG TATATTCTTT CTCTGTTTAT 960
TGCCCCCTAA CCTTTTTTTT TTTTTTTTTT TTTTTGGAGA CAGAGTCTCT CTCTGTCGCC 1020
CAGACTGGAG 1030