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

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EnhancerAtlas ID
HS187-16917 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr3:35337130-35338480 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE40MA0464.2chr3:35337580-35337590ATCACGTGAC+6.02
Foxq1MA0040.1chr3:35337841-35337852AATTGTTTATT+6.02
MITFMA0620.2chr3:35337576-35337594TTTGATCACGTGACCCTA+6.38
MITFMA0620.2chr3:35337576-35337594TTTGATCACGTGACCCTA-6.38
MNX1MA0707.1chr3:35337475-35337485TTTAATTACC-6.02
TFEBMA0692.1chr3:35337580-35337590ATCACGTGAC+6.02
USF2MA0526.2chr3:35337578-35337594TGATCACGTGACCCTA-6.52
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr33533803535338359
Number: 1             
IDChromosomeStartEnd
GH03I035296chr33533803535338359
Enhancer Sequence
TTTGAACATA CATTAGTTGG TCTTGAGCCC TATACTTCTT TTCTCACATT TCTGGGAGTC 60
GCTTACTGGC ATTCCCCTGA GGCCTGATCT CACTGGGCAG GTATTGCTGA TAATAATAAA 120
TGATGACAGG GCCATGCTTT GCAGCTTGGA GTAGTCCCGT TTGTATTCGA TTTCTGCACT 180
ATCCTAGGAA TTTAGATAAC TAAGGCAGAG TTCCCTTTTT TTCCCACTTT CCCCATTACC 240
AAAAAGTTCT TATGCTCAGG TTCTTTTGAT CCTGGCATCT TCATTGCCAT CAAAATTAGT 300
TATTCTGTGA CTCTTGTCAT CTTGGAACTG TCTAGGAATA TCATATTTAA TTACCACTTT 360
GCCAAGCTGT GAGTCCTTGC ATCAGTCACC CACCCTCTTT GATTCTATTT CCTCATCTGT 420
TTAATCAGAC AAGATGATCT CGAACCTTTG ATCACGTGAC CCTAAATCAG TCTTTCTCAA 480
CCCCAGCACT ACTGACATTT TGAGCAAAAT AACTCATTGT TGTGAGGAGC TGTCCTGTGT 540
GTAATAGAAT ATTTAGCAGC ACCTCTGACC TCTATACAAG ATACCAGTAG TAAATAAGAC 600
CCCTTCCTAG TTATGACCAT CAAAGATATC TCTAGACATT GCTGAATATT CCCTGGGTAG 660
GGGCAAAATC ACCCACAGTG GTGAACCATC ATTCTAGACC CATATCAAGA AAATTGTTTA 720
TTTTTACAAA ATACTAAGAT AGGTGCCATG CAGTTGTCTA AAAAAAATTT TTAAGCATAG 780
ACTATCCTAA AATATAAATC TCATATTCAG TAGAATTCCA CTGTCTCCCT TACCATTCCC 840
ACAAAATTAC ATGTTCTTTT TCTTCTCTTT CTGCCCTGTT TAAATGCTGG TTCTGCACCA 900
CCAGATGTGG TCTGATCAAG GCTCTCCTGA CAGTGTGCCT CTGACCCATG CAATCTACCA 960
CAGCTGGTGC TGCTACGTTC AGTTACATCA CTTTTTCTGT TATTGCAAGT GGGCCTGTTT 1020
CAGTCTCAGT CTTTGTGACA TCTGGTTGTT CTCTCCTTTC TAAAATCCTG TTTGCACAGC 1080
CACTTTCATC CCACTCTGTT CCCACAAGAG AAAGAGGTTC ACACTTTCTT TTTTGTGGTT 1140
GACCCTATTG TGAGAACTGG TGACTGTTGC GGTGAGCCAT ATCAACGAAG AACTGTTTCT 1200
TCATGTGGGC TTGTCTGAAA GCAACTACAG TGTTGTCTTC TCTCAATGTG CACGTCTCTG 1260
CACTGGGCTA GTTAAAGAAG TTGTAGAAAT AATAATCAAT TTATATGCAT TCTGATGCAA 1320
TGAAATTAGT ATTTGAAAAT TTATGTTTTG 1350