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

TagContent
EnhancerAtlas ID
HS003-30972 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr22:29260560-29261710 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF1AMA0046.2chr22:29261141-29261156GGTAAATCATTAACT-6.71
HNF1AMA0046.2chr22:29261141-29261156GGTAAATCATTAACT+6.82
HNF1BMA0153.2chr22:29261142-29261155GTAAATCATTAAC-6.46
HNF1BMA0153.2chr22:29261142-29261155GTAAATCATTAAC+6.82
SPICMA0687.1chr22:29261598-29261612AGAAAGGGGAAGAA+6.03
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr222926108829261244
chr222926100429261197
Number: 1             
IDChromosomeStartEnd
GH22I028865chr222926100429261197
Enhancer Sequence
AGCCACCAAG TTTGTGGTAA TTTGCTACAG CAGCCCTGGG AAAATACTAA TAGGCAGGAA 60
GCTGGAGCGG GGAGCAGCAA AGTCAGGGGA CAGGGAGCCC AGACTAGAGG CTGGAGAAGA 120
CCAGGCATGT AGCAGGATGA GGCGTGCTCA CCTCCCACAC GCACCAGGAG CAGGGCAGTC 180
CTCTTACTCA TAGGCAGGTC CATTCCCCCA GGGCTAGGAG GATGGGGTCT CTACCTTCAC 240
TATTTTCTTT AGAAAGAAGA AAGAAAGAAG AAAGATAGTG ATGGCGGTAA GGACAACAGG 300
GCCCTCGGGG GCACATGGCT ATGCTGTGGC CTGGAGAGAG GCAGACTCTT CTCAGAGGAG 360
GCTAAGGGCC TCTGGCTAGA GCATGGCTAC AAGCAAGGTG GCTAACATGA AGAGACCATG 420
GTGCAGAGGC AGATGCCAGC AGGCTAAAGG ACAATTCTGG AATGGGGCAG TGGGAGGGGT 480
CCTGTGTCTT TGGGCTTCTT TGATCCCTGA GACACTTTGG ACGGGACAGA GCCTTGGCCA 540
CCAACGGGGT CATGTCTGTT TAAACAAAAT TTAACACAGG AGGTAAATCA TTAACTCACT 600
GAAGAAACAA ACAGGAGTGC AGGCCATATC TCTAGCACCA GGATTCAAGA GCCACGGGGA 660
TGTTAAGAAC TCCTGAATAT CAGAAGTGGC TGCCACTCAT GGCTTCTGTA AGTGAGTGAA 720
AGCATTTGGT GAGCACCTTC TATAAGCAAG TCTTCGTGCC AGGTGCTGTG GGAACAGATG 780
CATGAAGAGG CTCAGAGTCT GACCTGAGCT TGGAGCTGGG GGAATACGAG CTCACAGCCA 840
TTGTGAGCAT GCCCATGCCT GTCTCCAGGC CCACCACGGC CCATCCATCA TCTCATGTAA 900
TTCTCATGCC TCTGAGGTAG GGCAAGGATT GCCTGCATTT CATAGACAAG GAAACCCAAG 960
CTCAGAGAGG GAGAGCAACT TGCCTCGGCC ACACAGCTTG TCAGTGGTGG AGAAAAATAA 1020
ACAGGAGCTG GCTTTTGCAG AAAGGGGAAG AAATTGTTAG GGTTCAAGGA TGTGTTTAGG 1080
AACTTAAGGG CAGGAAGCAC AACTTCCTGA AAGACAGGAG CCAGGTCCAG CAAAGCCATC 1140
AGGAGGCAAG 1150