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

TagContent
EnhancerAtlas ID
HS101-03596 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr1:201237520-201238550 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr1:201238177-201238191ATTCCCCAGGGACC+6.84
GSCMA0648.1chr1:201237869-201237879GCTAATCCCC+6.02
Nr5a2MA0505.1chr1:201237750-201237765GCTGGCCTTGGACCC-6.24
ZIC1MA0696.1chr1:201237692-201237706CACAGCAGGGGGCT-6.01
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_26526chr1:201237453-201239549Esophagus
SE_35843chr1:201234594-201238839HMEC
SE_37062chr1:201234857-201239624HSMMtube
SE_64243chr1:201234398-201239013NHEK
SE_68514chr1:201210031-201254923TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1201237679201238422
chr1201237729201238000
Number: 1             
IDChromosomeStartEnd
GH01I201265chr1201234755201239296
Enhancer Sequence
ATTCCTGAGC CCCAGCCCAG ACCTGGGTGG GCTCCTGAAA TGTCCCTTTT AAAAGAAGTA 60
ATGCCAGATG ATTCTCACGC TCTGTAGTTT GAGAATCATT GGCTGGAACG AAGAGGGCTG 120
ACTAGTGACA AGAAACTGGT CTGGAGGAGT ATGCGGACAT GGCCAGTCTT CTCACAGCAG 180
GGGGCTGTGT CCAGCAGCCT GCAGGGACCC TGCACCACTC CACTCTGTCT GCTGGCCTTG 240
GACCCTCGAC GTGGCAGCCT GCCTTATCTG GGATAAGCTC GTCCTCATCG CAGAATCCTG 300
ATCCAGCTGC CTCAGCAGCA GCTGCTGCAG GGAGGGAGGG CGGTGGAGAG CTAATCCCCT 360
CTGCTTTGGC CCAACACCGA GGCAGAGCCA TCCCCCAGAA CCAGATCCTA CTACGGGAAG 420
AGCCTGACAG GCCATCTGGC TCTTCTTCCC ATCACTGCCA GACTCCCTTG TACCATGGCA 480
CTCCCACGTC TGGGTCCAGG ATGATTCATT CTTCACAGAG GCTTCGTCCA CAGGGAAGTG 540
TCCACATGCA GCGTCTGGGA GAGGGTGGAC ACTGGCTGGT GGCCAGGAGG CCATGTCTGA 600
TCTTGAGAGC CAGGCTGCAT GGAATTATCT GGTAAACGGG GTGCTGTCAT TGTTTTTATT 660
CCCCAGGGAC CAGGCCCCTC CCTTGCTCAA AAGAGTCTAC TATTAGTTAC CTTGGGTCCC 720
AAACACCAGG ATTCTGCGAG TCTACCTGAG TGAGAATCAG GGGCTGGATG TCTGCCAAGA 780
CTCACTTGTC TCTTCTTTTC TCTCTGTGAC TCTGCTTCAT TCTCTCTTTC TCTCTCTCTG 840
AAGCAGGGTT CTCTGTATGC CAGACAACAT GTTAGACAAA TAGGCTCCCC GCTACCCAGA 900
GAGGCTCATT CCCACAGAGT CCCGATTCCA TATTCAGGGT TACTGTTTGG AGCAGTTCAG 960
GTCAGCTGGA CCCCTAAAGG TCCATGTCAC CGTCATGGCT CCTGAATACC AGGGCACGCG 1020
CTTTCTGAAA 1030