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

TagContent
EnhancerAtlas ID
HS028-03251 
Organism
Homo sapiens 
Tissue/cell
Colo829 
Coordinate
chr6:3247310-3248630 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr6:3248079-3248090GGTGACTCATG+6.62
JUNDMA0491.1chr6:3248079-3248090GGTGACTCATG+6.02
RESTMA0138.2chr6:3247715-3247736CCCAGCACTCAGGACAGTGCC+6.6
TBXTMA0009.2chr6:3248510-3248526TCACACATATGTGCAA-6.48
TBXTMA0009.2chr6:3248510-3248526TCACACATATGTGCAA+6.49
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
CACTGCACTC TAGCCTGGAC AACAGAGTGA GACCCTGTCT CAATTTGGAA AAAAAAAAGG 60
TGCACTGACC ACGGGTGTCC AGCATTCCAG AAGCCCACTT GGTGTTCTCC TCATCTCCTA 120
CCCCAACAAG CAGCTACTGC CTTGCCCTCC AGCAGTAGGT GTTAGCTCTG CAGGCTTCAG 180
GAGTTGATAG AAATGGAATC CGACAGTATG TACTCCGTGT ACATTCTTTT TGTGAGACTC 240
ACCCGTGTTC TCGCACATTC CATAAGCATC CCATGCATTC CTAGCTCCTT TAGATGCTGT 300
GAACTGGGGA CGGTTGACTG TGTCGTATTT ATGTGTGTGT CTGCCTCCCG GTTCCAGCGG 360
AGGGCGAGGC GGGGGTCATC GTTCTGAAGG GCATCTTTGT GTCTTCCCAG CACTCAGGAC 420
AGTGCCTGGC ACACAGATGC TTCAGTAAAT GTTTGCCGAG TGAACCCGAT GAATGGGCAT 480
TTTGTCACTG GGTCTTTTCA TTTATTCCTT GGCTTGCTCC CTGTCTCCCC TTGAAACACA 540
GCTGCTTTCA TTGACCGCGT CTTTATTTGT TGGGTGGATG TGCTTGTTTT CAGTGCCAGG 600
AAGGAAAAAC AAGCACAGAA GTCGCCCCTC CCGGGCAGCC ATATTCCCGG CTAAGAAGCC 660
CTCCTTTGTG CCAAGAGCAG AACCGTCTAT GGCTGGGTGG AGGGTCACAG CCTGTGGGAC 720
GGTGCGGAGA GGCAGGGGGG TGCGGCGAGC TCTGGGCTTG CAGGCAGGCG GTGACTCATG 780
CAGAGTCCGG CCACCGGTGC GGGAAAAGGG CTTTGACGTT CTCAGCAAAA CCCCAAGGCG 840
AGCTCCGAGC AGCCCACCTG CCCCTCCCAC CCACGCAGGG CCTTGCAGAT GAATCTGCTT 900
CTGTATCACA TGATCCGTTT CAGCAGGAGA GAGACGGAGA GAAACAGCCT TTTGTTCTGC 960
CAGCCTCCAT GATTGCGTAT CTTAGGCACA ACGCTCTGAA GTCAGGCTGA GGATTCTAAT 1020
AAAACTTGGG AAGCTTTACC CGGAAGACAA GGTGCTCTTT CACTAGGCAT GATTTGGACC 1080
CAGGATATAA ATTCTCTTTC GTGGGACGGG AGAGTTGTGT CTTTGCTTAT CCTCGGGGAG 1140
TCTCACTGTG CCCCACTGAT CATGCGTGCC TTCCAAAGCT GTCAGGTAGC CCCTCCACAA 1200
TCACACATAT GTGCAACCAC ATATTTTCCA ACCCAAACGA GGGTACACAC CATCTGGGGA 1260
GGGATTCCCC CTTCCCATAT GCGTGAATTC GTTTAGCTAA AAAGCATTAA CAGTCACAAA 1320