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

TagContent
EnhancerAtlas ID
HS108-12356 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr14:75700770-75701700 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4899554chr1475701221hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr14:75700959-75700980AAAAAAAAAAAGAAAGAAAGA-6.25
IRF1MA0050.2chr14:75700969-75700990AGAAAGAAAGAGAAAGTCAAG-6.96
RREB1MA0073.1chr14:75701313-75701333CCCCACCCCACCCGCCACAG+6.18
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_25845chr14:75700606-75701838Duodenum_Smooth_Muscle
SE_26738chr14:75700953-75701671Esophagus
SE_28748chr14:75700247-75701790Fetal_Intestine_Large
SE_37398chr14:75700795-75702224HSMMtube
SE_50151chr14:75700862-75701786Sigmoid_Colon
SE_52363chr14:75700038-75701856Small_Intestine
SE_53348chr14:75700993-75701872Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr147570090275701698
chr147570137975701456
Number: 1             
IDChromosomeStartEnd
GH14I075233chr147570042075702502
Enhancer Sequence
AAACCCTGTC TCTACTAAAA ATACAAAAAT TAGCTGGGCA TGGTGGTGTG CACCTGTAAT 60
CCCAGCTACT AGGGAGGCTG AGGCAGGAGA ACTGCTTGAA CCCGGGAAGC GGAGGTTGCA 120
GTGAGCAGAG ATTGTGCCAC TGCACTTCAG CCTGGGTGAC AGGGAGAGAT TCCATCTCAA 180
AAAAACAGAA AAAAAAAAAA GAAAGAAAGA GAAAGTCAAG AACAAAGTTT CTTCATGAAC 240
AAAGGGCATG AAGAAACCTG TTCAGTAGCA GCGGGGCTGT TCAGTGGGGC CAATGTTCAG 300
TGGGGATAGT GAGACCAGAG GTTGAAAGCC GGTAGAGAGT ACAGAAAAGG TGGACAGAAT 360
ACTAAGACAA AGTACCGTGT ACTTTCAATA AGCTCTTGGT CTCAACTCTT GGTGACTGTA 420
CAAGGTAGGC CAAAGACAAA AACTGTCCAA CGACAGAAAT TTCACTTTGA AGTTCCCTCC 480
ACTCCATTTC TCCACCCCCT TCCTTCCTAT CTCCTTTAGC AAAGTCCTTT CCTCAGAGAT 540
CTCCCCCACC CCACCCGCCA CAGCCCCACA GCCCTGTCGG TCTAGCAGGG TGAGTAGCCG 600
CACTGTCTCT GAACCCTTAC GCCTGGACTT TGAAGGGGGA ACAGATTCTT GCTTACTGAG 660
TCAGCCTCGG CTGCTTCCTT TTTGTGCTTG AAGAAGCCAA AGAGTGAGCA GATTGGAGAG 720
GACTAAAAGA AGCCAGAGAT GCTGGTCAAT TGACACAAAA ATAAAGAGCT AAGGGAGAGG 780
TTGAGAGAGG GAGAGCAATA TCTATGGGTG TCTGGAATTT TTAAAGGGCT CAGAGGAGGA 840
GGGGGCCGGG CGTGGTGGCT CACGCCTGTT ATCCGAGCAC TTTGGGAGGC CAAGGTGGGC 900
AAATCACGAG GTCAGGAGTT TGAGAGCAGC 930