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

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EnhancerAtlas ID
HS177-18998 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr6:3247290-3248480 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr6:3248079-3248090GGTGACTCATG+6.62
JUNDMA0491.1chr6:3248079-3248090GGTGACTCATG+6.02
RESTMA0138.2chr6:3247715-3247736CCCAGCACTCAGGACAGTGCC+6.6
TEAD1MA0090.2chr6:3247563-3247573CACATTCCAT+6.02
ZEB1MA0103.3chr6:3248162-3248173CCCACCTGCCC+6.14
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr632480623248427
Number: 1             
IDChromosomeStartEnd
GH06I003246chr632468563249920
Enhancer Sequence
GTAGTGAGCT ATGATCACAC CACTGCACTC TAGCCTGGAC AACAGAGTGA GACCCTGTCT 60
CAATTTGGAA AAAAAAAAGG TGCACTGACC ACGGGTGTCC AGCATTCCAG AAGCCCACTT 120
GGTGTTCTCC TCATCTCCTA CCCCAACAAG CAGCTACTGC CTTGCCCTCC AGCAGTAGGT 180
GTTAGCTCTG CAGGCTTCAG GAGTTGATAG AAATGGAATC CGACAGTATG TACTCCGTGT 240
ACATTCTTTT TGTGAGACTC ACCCGTGTTC TCGCACATTC CATAAGCATC CCATGCATTC 300
CTAGCTCCTT TAGATGCTGT GAACTGGGGA CGGTTGACTG TGTCGTATTT ATGTGTGTGT 360
CTGCCTCCCG GTTCCAGCGG AGGGCGAGGC GGGGGTCATC GTTCTGAAGG GCATCTTTGT 420
GTCTTCCCAG CACTCAGGAC AGTGCCTGGC ACACAGATGC TTCAGTAAAT GTTTGCCGAG 480
TGAACCCGAT GAATGGGCAT TTTGTCACTG GGTCTTTTCA TTTATTCCTT GGCTTGCTCC 540
CTGTCTCCCC TTGAAACACA GCTGCTTTCA TTGACCGCGT CTTTATTTGT TGGGTGGATG 600
TGCTTGTTTT CAGTGCCAGG AAGGAAAAAC AAGCACAGAA GTCGCCCCTC CCGGGCAGCC 660
ATATTCCCGG CTAAGAAGCC CTCCTTTGTG CCAAGAGCAG AACCGTCTAT GGCTGGGTGG 720
AGGGTCACAG CCTGTGGGAC GGTGCGGAGA GGCAGGGGGG TGCGGCGAGC TCTGGGCTTG 780
CAGGCAGGCG GTGACTCATG CAGAGTCCGG CCACCGGTGC GGGAAAAGGG CTTTGACGTT 840
CTCAGCAAAA CCCCAAGGCG AGCTCCGAGC AGCCCACCTG CCCCTCCCAC CCACGCAGGG 900
CCTTGCAGAT GAATCTGCTT CTGTATCACA TGATCCGTTT CAGCAGGAGA GAGACGGAGA 960
GAAACAGCCT TTTGTTCTGC CAGCCTCCAT GATTGCGTAT CTTAGGCACA ACGCTCTGAA 1020
GTCAGGCTGA GGATTCTAAT AAAACTTGGG AAGCTTTACC CGGAAGACAA GGTGCTCTTT 1080
CACTAGGCAT GATTTGGACC CAGGATATAA ATTCTCTTTC GTGGGACGGG AGAGTTGTGT 1140
CTTTGCTTAT CCTCGGGGAG TCTCACTGTG CCCCACTGAT CATGCGTGCC 1190