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

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EnhancerAtlas ID
HS076-00658 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr1:15714390-15715610 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:15714777-15714795CCCTCCCTCCCTCCTTCC-7.12
ZNF263MA0528.1chr1:15714777-15714798CCCTCCCTCCCTCCTTCCCTT-6.05
ZNF263MA0528.1chr1:15714769-15714790CCCCTCGTCCCTCCCTCCCTC-6.18
ZNF263MA0528.1chr1:15714741-15714762CCTCCTTCCCTTCCCTCCCCA-6.41
ZNF263MA0528.1chr1:15714786-15714807CCTCCTTCCCTTCCCTCCCCA-6.41
ZNF263MA0528.1chr1:15714737-15714758CCTCCCTCCTTCCCTTCCCTC-6.61
ZNF263MA0528.1chr1:15714782-15714803CCTCCCTCCTTCCCTTCCCTC-6.61
ZNF263MA0528.1chr1:15714773-15714794TCGTCCCTCCCTCCCTCCTTC-6.76
ZNF263MA0528.1chr1:15714819-15714840CCTCCCTCCCTCCCCTCCCCA-7.06
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11571483815715400
Enhancer Sequence
GAAAAAGACT CTCCCGCAGT GATCCCTTAT CTTCTGCCCA CCTATCTCAG TGAGTCCCAG 60
CGTCTCCTAG AAACCTCAGA GGCCTGTCCC AGATTGGAAC GGGTAAGGAC ACACTAAGGT 120
TAGCACTCTC TTGCTAACCT GATACTTTTC ACTCAGGAAA GTGTAGAGGA GCACGAACTG 180
AGAAACGCAA AAGAATCGAC ACCTTGCAAC TGTGCCTTCA AAGAGAAAGA CAGGCAGGTA 240
TGGGAGGTGT TCTGATGTTG CAGACACAGA GTAGAGACAG TCTCAACTGG GGGTAAGAGC 300
TCATGGCATG CAAATGCCTG CACGCGCTGC CCAAGGAGCA CTGCACACCT CCCTCCTTCC 360
CTTCCCTCCC CAGCCTCTGC CCCTCGTCCC TCCCTCCCTC CTTCCCTTCC CTCCCCAGGC 420
CCTGCCCCAC CTCCCTCCCT CCCCTCCCCA GGCCCTGCCC CACCTGCCTG CAGTTTGAAC 480
GGATGACCTA AGAGACAAGC ACGCGTCCAG CCCCGTCTGT CCATTAAGGT GAGAAGGCAG 540
AGGGGATATT CCAGCACAGC TTCAGCTCAT GGAGCAGCCA TCCTAGGCCA CTAAGTAACT 600
TGGGGACTTG GAGGCAAGGT CCTAAGAGAA GAAAGAAGGG AGGAGTGAGG AGCTTCAGGA 660
ATCCCTGTCC TAAGAATGAA ATGAGGGGGG TGAAAGAAGG TGGGAGTGGC TACAAAACAG 720
AGCCAGGAAT GAGGATGAAA GTGCCTCGCA TAAGCACTTC TACCCCCGCC AAGGGGAGCC 780
CTGTTTTACT CCGACCTTCC TGGCAGCCAA CGAGAAATGG GAAACCAACT TGGTCACAGT 840
TCACAGTGTC CATGAGATAC AATGGATGGA TGCTCGTAAG TGCTCTTAGA ACAAAGACCT 900
TGCTGGACTT TCCCCCTAGA GGGGACGGTG TGTGACGTAA AGAGCAGCAT CTTTAAGAAC 960
AGCCTTCGTG GGGTGACATG GGCTGAGCCG TGGCTGAGAA CAGCTCTTGA GACAGATCGA 1020
TGTCATCACA TCCCACTGAA TCCAGTAAAG TTCAGTAAAG CAGATCTGTA CGGGGCTGGG 1080
CTCTGCTCTC CAGTGCTCAG GTGTCCACTG AGCAGACTTA ATCCAGGGAT GGATTGTGGA 1140
GCAGTGTTCC ACCTGGGATT CCTGGAGCCC TTGTGCCCCG TGGAAGGGTA TGAGTCCCAA 1200
CATCCTCACA TCTTGTTTCC 1220