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

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EnhancerAtlas ID
HS177-02060 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr1:229546400-229547190 
Target genes
Number: 4             
NameEnsembl ID
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MyogMA0500.1chr1:229547042-229547053GACAGCTGCAG+6.62
Tcf12MA0521.1chr1:229547042-229547053GACAGCTGCAG+6.14
ZNF263MA0528.1chr1:229547098-229547119CCTCTCCCTGTCCCCTCCTCC-6.24
ZNF263MA0528.1chr1:229547161-229547182CTTCCTTCCCTTTCCTCCCCT-6.39
ZNF263MA0528.1chr1:229547125-229547146CCCCCTCCTCCTCTCTCCTCT-6.51
ZNF263MA0528.1chr1:229547101-229547122CTCCCTGTCCCCTCCTCCCCC-6.7
ZNF263MA0528.1chr1:229547121-229547142CCCTCCCCCTCCTCCTCTCTC-6.86
ZNF263MA0528.1chr1:229547065-229547086CCCTCCCCCTCGGCCTCCTCT-7.1
ZNF263MA0528.1chr1:229547109-229547130CCCCTCCTCCCCCCCTCCCCC-7.68
ZNF263MA0528.1chr1:229547115-229547136CTCCCCCCCTCCCCCTCCTCC-9.53
ZNF263MA0528.1chr1:229547118-229547139CCCCCCTCCCCCTCCTCCTCT-9.77
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1229546837229547142
Number: 1             
IDChromosomeStartEnd
GH01I229406chr1229542447229548197
Enhancer Sequence
AAGATTCTCC TCTTCCACCC AGCACGCAGC TTCAGGAGAG ATCCACATGG AGCAGTGAGG 60
GAGGAAAGGG ATGCCTGCCT AAGCCAGCAG GTGTCAACCC ATTCGAATCA ACCCTCTGCA 120
GAATGGTAGC CCCAGGCGGC GTGCCTGTCA TTTGCTCTGA TCATCTATTA TGCGCACCGC 180
ATGATAGCAG CAGCCCCCCA CCATCTGTTT AGGATCCTTA TTATGTGGGT GTCACATTTA 240
AGTGCCTATT AGCACAGCTT CCCTGAGCCC CTCCTGCAGC TGCTACCACC CTTTGGTGCC 300
AAAGCCCAGG CGGTTGTTCT TGTTGACTCT GTTCTCCTTC CCAGAACACT GATTACTGCT 360
GGGAGGGCTG GCAACTCCCC ACAGCCCTCT AGAGCAGCAG CTGAAAGCGC CTGGTTATTA 420
AAAAGGCTTA GAGCTCCTGA TAAGAGAGAA GGATCGCTTT ATAATTCCTA TGTAGACTTC 480
TAAATTATTC CCTCGGCCCT CATCCTCTGC CACCAGATTC CCCTCCACCA GTTGGAAGGC 540
TTAGTTAACG AGTCAGATAT GAGCAGGCGC TGATATAAAA ATAGAGGCAG GCAGTGGGAG 600
CTGGCACTGT GACTCACCGT GTGGCAGGCG TGGGGCTCTG CAGACAGCTG CAGGCAGGCC 660
TTATGCCCTC CCCCTCGGCC TCCTCTTCCC CTCCCCTACC TCTCCCTGTC CCCTCCTCCC 720
CCCCTCCCCC TCCTCCTCTC TCCTCTCCTA GTTCCCTCTC CCTTCCTTCC CTTTCCTCCC 780
CTTTCCGTCT 790