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

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EnhancerAtlas ID
HS147-04910 
Organism
Homo sapiens 
Tissue/cell
NHEK 
Coordinate
chr1:231913230-231914410 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr1:231914002-231914012GCCCCGCCCC+6.02
MEF2AMA0052.3chr1:231913891-231913903TCTAAAAATAGA+7.22
MEF2CMA0497.1chr1:231913889-231913904TATCTAAAAATAGAC+6.68
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1231913684231914345
Number: 1             
IDChromosomeStartEnd
GH01I231775chr1231911245231915153
Enhancer Sequence
CACTGGGATT ACAGGGTTTT CTTTTCCCCC TACTCCCCTT TTTAAGTAAA GTAGACATCT 60
TGCTTTTCTC AGGAATTCAT GAGGCAGAAA AATATTTGCC AAGACAGCAA ATGCAGTGAG 120
ACAGAAGTGT GTGAGCAATG CTGGCCAGAT GGGTGCCCGG AGTGAGGCTT CCCTGCATAG 180
GCGACATCTG CAGCATTCAG GACCTCCCTG CAGGTGTGCC CTCTCCACTC AAATTTATCC 240
TGTCTGTCCT TCTTAGTTAG ACTGGTGTTG ATACTCATAC ACTAATTTTA ATATCTCTGT 300
TATTTACAAA CTGTCATACT TGCTTACAAT AACCCTATAA GGTTTGTTGG GCAATATATT 360
GTTTTTATGC CCATTTTGCA GATGAGGCTG CTGAGGGTCC AAGTTCACAC AGCCGTAAAA 420
GCAGTGCCCT CACGTCTTTG GCGAATTTTT AATGCAGAGG GAATCCAGAG ATGGTTCACA 480
CTGATGGCCT GGGAGAGACC AGGCCTTGGA CAGAGTGCTT AGTCCAGCAA TGGAAAGAAG 540
TCCAGCCCAG CAGAGCCGTG GGTCTGTGGG CCCAAGGAAA AGAGAATGGA TGTCCCTCCA 600
GGCCAGGGAT GGTTGTCTCT GTGTGCCTAG TGTTGCCTGA TTGGATTGGA GCCAAGGTGT 660
ATCTAAAAAT AGACAGCCTG GGAAGACCAA ACAGGCAACT GTCTCAAGTC AGAGAGGTCT 720
GTCAGACGTT CCAAAGAAAG AAATGTGAGA GGAAGAGAAA CTGGAAAGCA AGGCCCCGCC 780
CCAGGGCTAG AGGAACTGGT ATTACTTGTC TGTGAAAAGA GGGTTTGAAC TGGGTGGCGT 840
GGAAGGTCTT TTCTGGTTCT ACAATACTTT GCACTTTAGT ATTTTATGAA ATAAGTTAAA 900
ATAAGCTGCC TAAAAACCCC TCATAATTCT ATTCCTAGGA GCTCTATGTT AAGTTCCTCC 960
TTAAAGTTCC CTGGGCAGGC TGTGACCATC CACAGGCCAC GGTGCTCCAG CTGGCACTTT 1020
CCTTAGGGCT GGTCCCTAGA GCATGGACCT GAGCAAAGCC TGCTTTCCAA GCACTGCTGC 1080
TGCAGCTCAG AGCTTAGACC TCGCCTCACC ATTGTATATC CTCCCGTTTT CTTCTGGAAA 1140
GTCGTCATTA CAGGCAACGT GGAAAAGTTT ACCAGACTAT 1180