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

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EnhancerAtlas ID
HS129-03498 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr1:222719580-222721060 
Target genes
Number: 7             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr1:222719935-222719947AAATAAACATTC-6.74
RREB1MA0073.1chr1:222720358-222720378CCCCCAAACACCCTCTTCCT+6.05
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1222720670222720836
Enhancer Sequence
AACTATACTT TAGCACGGTG TGATCAAAAG GCACAAAACT TGGAGCCTGA GCATCTGGCT 60
CTGTGCCCCA GGATTGTTTT ACCTTGGGTA AGTCATCTAA ACTCTTGAGC CCTCATCAGT 120
AAAATGAGGA TCATAACAAC TGCCTGCAGA ATCATTGCTG GGTACACACT ACATACGTTG 180
GGGAAGAAAG AGGACCTTAT AAATGTGAAT AAATAAACAC GTGTAGGACT GTTTGGCTGA 240
AATTGTTCTT ATTCCTCAAA TCCCTAAAAC AACAGAGCTG CTGACTTTGA CTTTCTGAAA 300
CCTCATGCAA GAGGGAAGGG TCAGGGGTAT AAATTTTTAC CAGGGATGAT CTCAGAAATA 360
AACATTCTCA GTGCTGCTTG TAAAAGCTCA GCTTCTACCC TAATGGGAAT CCTAGAGTTA 420
ATTCTCCAGG AAACAGCTGT GGAGTGGTGT CTAAGAGGAC AGCCCCAGGC GGTGCCACCC 480
AGGTGGCTGA CTTTCTGGGC CAGGCTCAGC TGTAATTCTC TCCTGGACTC TGGGAAGCTC 540
GGTTAACCAC TTCACGCCCT ATGTGGGAGT TACAGTGGTC TGCAGGCTCA GGAACAGTGG 600
CGCCAGGAGT CATGAACAGA TGCCTGTGGA TAGCCAAGTC ATTGTGCTGA CAAGCCCAGG 660
GGGTCTCAGT TCAAAAGGCT GCCTGGACTT CTTGCCTCTC CTCCCCAACA TCATTAGAGG 720
GGTCCTCCCC AGGCAGCCTC TTTTATCAGC TTTCCAAATG CTGACCTCTC CCCATTAACC 780
CCCAAACACC CTCTTCCTAC AAAGTCTGTG TGTGCAGCCT ACACCCGTCT TGTTTTCAGG 840
CTGAGCTCAA TCAAAACGAT GCCTCCCAGG CATGTGGATT TTGGCTGTTG GGCAACCAGG 900
AGAAGCAGAA ACTCTGTGAG TCACTGCTAC TCAGCAGCTT GCATCTCTCT CTTCCAGCTC 960
TGGAGTGCTG GGCAGACAGA ACTCTGGAGA GAGTCTCCAA CCCCTGCCAC CGCCAGGGTG 1020
ACGCCAGAGA TGCCCTGGCA CAAATCACCC AGATGAAAAG GACTGGACCC CAGCAGATGC 1080
CACCACTCCC TCCCTTAACG CGCTCGGTAA ATTCCACGGG TTTAAGTGCC TAGCTCTCTG 1140
AGCACCGCAG AGGATGCAAA TAATTATTTG CCATGCACCA CAGAGGGAGT GTGGCAAATA 1200
ATGGCTGCTC TGAGAGCTCC AGGAAGAGTG TCCCTCTCAT TCTCCTGGAG CCTGGAGAAG 1260
AATCAGGGCC AGCAGAATCC CAGAGGGAGA GCTTTGGGGA ACCCATGGAG ACCAAATTCA 1320
GCACACACTC ATGTCAGTGT GCGTGTCCAA AGCCGGCAGC TCCAAGATGA GGCACCCGGC 1380
ACATGAACTT CTAAAGGGCT GGGCTCCCAA AGCACCCTCC GCTCAGGACC CACACCATGC 1440
AGCCCAGCAC CCAAACCCCT GGGGCTGGAA GGCACTTTTC 1480