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

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EnhancerAtlas ID
HS105-07659 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr1:232278130-232279600 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SREBF2MA0596.1chr1:232278681-232278691ATCACCCCAT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1232278296232278454
Number: 1             
IDChromosomeStartEnd
GH01I232142chr1232277824232279897
Enhancer Sequence
ACCATGAAGA AAGGATCCCA TCCAGACTAC AGGGAACAGA CTGAGAGACC TCAGTGGCTT 60
CCAGTTGCTA ATGTGTGTGA TTCCCACACT GGGTAACACA GGAGTGTTTG ACCAACAATC 120
AACTGAATAC TGGTTCTTGT TTCTCATTGT CATGGAATTT GCCGAATCTC ACTTTTGGCT 180
TCACAGAGGA CTTTGTGAGC TCCAAGCATG AAAAGTGGCA TTTATAACTC CCCCTGGAAT 240
TTCCATGTAC CCAGGACACT GCCAGGCCAA AGGATGAATC ACAGCTTCTT AGAATTGTGG 300
AAGCCATTTT GGAAACAGCT GCCAAGTAAC TAATGCTATT AAAAATAGCT CCCTAAAAAA 360
TGAATTGCTT ATTTTAAGAA GACAAGAGTG GCTTGAATCT GTGCTGCTCA CATTTTTCAT 420
CTACTGGGCA CAGTGCCCGT GGATCCAAGA AAGCCCTGCT TGTCAGATGG GAATACCATC 480
TGTACAGATG ATGCCCCGCA CATGCAAGAG CCTGGCATTT TTGGGCCAGG GCTAACCAGG 540
GTAAAGTCTG AATCACCCCA TGTGGAATCC GTCTCCTACG GGGTGTGGAC TGTGGGGCAT 600
GAATTCCAAT TGCGCTTTCC TTACATAACT TTGCTCTTCA GATCCCTGGT TCCGAATGTG 660
GGGTGTATGC AGTATGGCCC ACTGGAAGTA CATGAAAATG CTAGAAGGTG AATCTACATG 720
TATTTTTTGA TCTAATGAAA ACAAGCAGGA AAATAAGTTG TACTGACAGG TAATGTGCAG 780
ACTGATACTG CTGTCTTGAC TCAGACTGTG TTGGGCAATT GTCTTTCCCT GTGAATTCCG 840
TGAAGAAATG AACCCATCCA GACCCATCCC ATGGCAATAG GATTGATGGT GCCAACCTCC 900
CATGTTTGTT TTATGCCCCC TGTGTTGTGA CGTGGGGCAG TTAACCTATT TCTGGCTTAA 960
ACAGTGTCAA AAATAAACAA AGCCAGGCAC TAGTTAAAGT GGTAAGAAGA GACTTCAATC 1020
AGCACTTTGA TTTGTGCAGC AGTGACTAGG CATTTTAAAG GAAGAATAAG GGAATGAGGA 1080
GAGGTGTGAG TGGGGACTCA GGAGAGTCAG GGAAGTGAAA AATCATCAAA GGCGGGAGGG 1140
AGGAAGCTTG GTCCATGTGG AAACTATCTG GATTTTCTAA GTGCTCCTTC TCAAAGCGCT 1200
GCCCTTCTGG AGGCTGGGAG ACAGGGTACT TATCTTCAGG TTTTGGCTGA AACAAACAGT 1260
AAATTCCTTG GGCAGCCCTG CATTTCTCAG GCAGGCACTT TAAGGAGATT AGGGGCATGC 1320
TAAGGATGTG GCCTTGAGCT GCTAGAAACT GTGTTTGTGT TTGTTCAAGC CTTTATAGGC 1380
CAAGGATGAG GCCTAGTGGA GAAGGGGGCT CAGTGGAGCC TGACTAGAAT TTGGTCAAGA 1440
AGAGAGTCTT TGTCAGTAGC CCTGCAGATA 1470