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

TagContent
EnhancerAtlas ID
HS101-16382 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr16:4997130-4998310 
Target genes
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr16:4997847-4997865GGAAGGGAGGAGGGACAG+6.04
ZNF263MA0528.1chr16:4997252-4997273CCCTCCCTTCCTCCATCCATC-6.06
ZNF263MA0528.1chr16:4997244-4997265CCCTCTCTCCCTCCCTTCCTC-6.08
ZNF263MA0528.1chr16:4997240-4997261TCTTCCCTCTCTCCCTCCCTT-6.84
ZNF263MA0528.1chr16:4997245-4997266CCTCTCTCCCTCCCTTCCTCC-7.13
ZNF263MA0528.1chr16:4997248-4997269CTCTCCCTCCCTTCCTCCATC-7.21
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_26593chr16:4997107-4998746Esophagus
SE_65358chr16:4991965-4999969Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1649973134997379
Number: 1             
IDChromosomeStartEnd
GH16I004947chr1649975504998710
Enhancer Sequence
CTCCATCCAT CCATCCATCC ATCCATCCAT CTCTTCATCC CTCCATTCCT CCATCCATCT 60
CTTCATCCCT CCATTCCTGC ATCCATCCAT CCATATCTTC ATCCCTCCAT TCTTCCCTCT 120
CTCCCTCCCT TCCTCCATCC ATCCATCCAT CCATCTATCC ATCCATCCAT CCATCCCTTC 180
ATTTGTCAAA TATTTACTAA GCACCTGCTA CGTGACAAGT CCTGTTCTAG GCACTCAGGA 240
TTCAAGATCA AGTACAATAG ACTCAGGTTC CTGCTCCCAG GGAGCTTGCT GTGGGAGACA 300
GGAGTGGGAA TGGACAAACA ATGTAAGTTT GAGGTCCCCT TGGGTGGATC ATGGCGCCTC 360
TTCTGTGTGC CCCAGGAGAC AAAGTCTGCA GTCGGCACAG AGTCACCGTC AGGTGGGGGC 420
CCAGGGACAC TATGAGGAAA GTGGCCAGAC TCCAGTCTGA GGGTGGTTGA GGACCCGGTG 480
AGGAAGGGGA GGCCTTAGCT TGCAGGGCGT CAGGTTCCCT CATCGTGTTT TCTGCATCAC 540
TGACATTTCC CAGGAGCCAG GCTCCTCCCC AACCCCCGTG GAGGATCTCG ACCTCTTGCC 600
CCCACAATAC CTCCCACAAG TCACTCATCC ATTTATTGAG CACCTACTGT GTACCCGGCT 660
CTGGGGATAT AGTAGCAAAC ACGATACATC CCTCACATCC TGGGGGCCCC CTGTCTTGGA 720
AGGGAGGAGG GACAGAAAAG CAAACAGATA ACCACATTTT TTACAAATGA AATAACCTAA 780
GTGCCCATCA GTGGGGGAAG CGGTGGTAAA TTACAAAACT GCCCTAGTCT GGGAGGAATT 840
CGGGGAGGCC TGTGGGCCTC ACAGGGAAGC TGAGGGTGTA GCAAGTGAAA AAAGGAAGCT 900
GCCTGCTATT AGGTGTCGTG TTTTGCCATT TCCGCTTCAG AACGGAGCTG CCCTGTGTCT 960
CCGTGAGCTC GTCCTCCACC TGCCTGCCTG CCTGGCTCTG CCTCCACTCT TTGTTCACGC 1020
TCTCTGCTGA GCTCAAACAT TCCTGCTGGG CCCAGGCAGC CAAGCCCCCA TCAGCCGCCT 1080
CCCAGGCCAT TCTCTAATCA CAAGCTCAGG CTTAATCCCC ACACACGCCC AGGACTCCGC 1140
TCTGGGCAAA TACTCCTCCT TTCAGCCCTG GAGTCCCTGA 1180