EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-06755 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr10:134261830-134263610 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PLAG1MA0163.1chr10:134263102-134263116GGGGCCCAAAGGGA+6.17
SP1MA0079.4chr10:134262092-134262107CTGGCCCCGCCCACC+6.51
SP3MA0746.2chr10:134262094-134262107GGCCCCGCCCACC+6.14
SP4MA0685.1chr10:134262092-134262109CTGGCCCCGCCCACCCT+6.67
ZNF263MA0528.1chr10:134262986-134263007GGAGGTGGAGGAAGGAGGTGG+6.01
ZNF263MA0528.1chr10:134262989-134263010GGTGGAGGAAGGAGGTGGAAG+6.32
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_09804chr10:134257271-134262186CD14
SE_09804chr10:134262886-134263621CD14
SE_12419chr10:134259518-134262324CD3
SE_20503chr10:134259305-134262317CD56
SE_20503chr10:134262606-134263523CD56
SE_23106chr10:134259138-134262223Colon_Crypt_1
SE_23106chr10:134262639-134263760Colon_Crypt_1
SE_23746chr10:134259695-134262253Colon_Crypt_2
SE_23746chr10:134262738-134263756Colon_Crypt_2
SE_24681chr10:134257175-134262451Colon_Crypt_3
SE_24681chr10:134262520-134263865Colon_Crypt_3
SE_27260chr10:134259879-134262285Esophagus
SE_27260chr10:134262486-134263511Esophagus
SE_32166chr10:134259274-134262295Gastric
SE_32166chr10:134262577-134263727Gastric
SE_34405chr10:134257518-134262215HCT-116
SE_34405chr10:134262859-134263631HCT-116
SE_41567chr10:134257195-134262212LNCaP
SE_41567chr10:134262912-134263679LNCaP
SE_47867chr10:134259977-134262132Pancreas
SE_47867chr10:134262749-134263307Pancreas
SE_50630chr10:134259441-134262281Sigmoid_Colon
SE_50630chr10:134262790-134263718Sigmoid_Colon
SE_52741chr10:134259687-134262225Small_Intestine
SE_52741chr10:134262747-134263550Small_Intestine
SE_53287chr10:134259455-134262313Spleen
SE_53287chr10:134262620-134263343Spleen
SE_57559chr10:134260530-134262070VACO_503
SE_60105chr10:134230766-134267420Ly4
SE_61428chr10:134196155-134334764Toledo
SE_65264chr10:134257981-134262203Pancreatic_islets
SE_65264chr10:134262621-134263604Pancreatic_islets
SE_68705chr10:134257192-134262075H9
SE_68705chr10:134262810-134263538H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10134262000134262158
chr10134262744134263336
Number: 2             
IDChromosomeStartEnd
GH10I132443chr10134257221134262630
GH10I132449chr10134262768134263397
Enhancer Sequence
TAAGGGAAAA TCAGCCCCGA CAGCCAGGGC TAACAAGACG GTTAATTACA GCCCGAGAAG 60
AACGTTAACA GTATTAATTC TAACCACAAA GGAGGAAAAG AGAAGACCGC CTAAGAAGGA 120
GAAGGAGGGT CCCTTTCCCA GATGAGGCTG CCCTAACCAC TGGGACCTCG GCCCCTCCCA 180
GGCCTGAGGG AGCCCAGCTC TGCCTGGCCC CACCCATCTC ACACCAGCCC TGCCTGACCC 240
GCCCACCTCA CCCCAACCCT GGCTGGCCCC GCCCACCCTT GCCTCAGCCC TGCCCGGCCC 300
CTCCCACCCT TGCCCAGCCC CTGCTTGGCC CCTCCCACTC GTCCCAACCC TTCGTGTCAC 360
CGCCAACCCT TGCCCCAGTC CGGCCCGGCC CCTCCCACCC TTGCCCCAGC CCTGCCTGGC 420
CCCTCCCACC CTTGCCCCAG TCCGGCCCGG CCCCTCCCAC CCTTGCCCCA GTCCTGCCCG 480
GCCCCTCCCA CCCTTGCCCC AGTCCTGCCC GGCCCCTCCC ACCCTTGCCC CAGCCCTGCC 540
CGGCCCCTCC CACCCTTGCC CCAGTCCTGC CCGGCCCCTC CCACCCTTGC CCCAGTCCTG 600
CCCGGCCCCT CCCACCCTTG CCCCAGTCCT GCCCGGCCCC TCCCACCCTT GCCCCAGTCC 660
TGCCCGGCCC CTCCCACCCT TGCCCCAGTC CGGCCTGGCC CCTCCCACCC TTGCCCCAGT 720
CCGGCCTGGC CCCTCCCACC CTTGCCCCAG TCCGGCCTGG CCCCTCCCAC CCTTGCCCAG 780
CCCCTGCTTG GCCCCTCCCA CTCGTCCCAA CCCTTCGTGT CACCGCCAAC CCTTGCCCCA 840
GTCCTGCCCG GCCCCTCCCA CCCTTGCCCC AGTCCTGCCC GGCCCCTCCC ACCCTTGCCC 900
CAGTCCGGCC TGGCCCCTCC CACCCTTGCC CCAGTCCGGC CTGGCCCCTC CCACCCTTGC 960
CCCAGCCCCT GCCTGGTCCT GCCCACCTCA CCCCAGCACT TCCTATGGGA CTCACGCCTT 1020
TGTCTCGGGC TTTTGGTTTT CAAAATAAAT TATAAGTTTT AATAAAATAA AGTACTAGAA 1080
AAGCTATTCA TTACGGAAGA TGTAAAAATC CGAAAAGAAA CTTCCATTTG GGAGGAGAAA 1140
TGGAGAACGG AGCCCAGGAG GTGGAGGAAG GAGGTGGAAG GCCCTGGGCC CTGGAAGGTT 1200
CTGTCTGTTC TCCAGGAACC CAGCTTCCAT TTACTCCCCT AAAGCAGAGG GATGCTCTGG 1260
GAAGGCAGGT GTGGGGCCCA AAGGGACCCT GATGAGGACA CGTGGGGTCA GCGGGGGTGG 1320
GGGCTGCAGC CGGAGCCGGT ACCAGGTGTG CCCCCCCATG CCACTCTGGA GCCGGTACCA 1380
GGTGTGCCCC CCCGTGCCAC TCTGGCCTTC AGCACGTGGA CGAGAAAACC AGCCCCTCAT 1440
GATGTGGATC CCCTCTTTAA ACTGGGCTGC ACTTCGGTCT ATAAAATATT CAGTGTCTTT 1500
CTAAATAATT GCATTATTTA TGATGCCGCT CGTGAAATAT TCATGTCTGA CTTTGACACG 1560
GAGCCAGTAT GCCCATGCAG GTCTGTGGCG ACGGGCTGGC CTTTCCCAGG TAATGGGAGG 1620
AAGTAGGGCT GCTGGGGTGG GGGGTGCTCG GGGAGTCGGT GGAGCCCCCT GGCAGGTGGA 1680
TCTCACCCGG GAGCCAGGGA TCTCCCCACT GGCAGCCTTG GGGCCTGCCT CCTCTGCTGG 1740
GGAGCTCATG AGTGGGTGGG TGGGCACCGG CTCCCCAATG 1780