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

TagContent
EnhancerAtlas ID
HS054-02158 
Organism
Homo sapiens 
Tissue/cell
FT246 
Coordinate
chr13:114301180-114302590 
Target genes
Number: 4             
NameEnsembl ID
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr13:114302067-114302078CTTTCCCGCCC-6.32
NR2C2MA0504.1chr13:114301751-114301766TCACCTCTGACCTCT-6.88
NR2C2MA0504.1chr13:114301758-114301773TGACCTCTGACCTTC-7.33
Nr2f6MA0677.1chr13:114301758-114301772TGACCTCTGACCTT-7.28
RxraMA0512.2chr13:114301758-114301772TGACCTCTGACCTT-6.62
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_41872chr13:114301246-114302949LNCaP
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr13114301674114302571
chr13114301802114302224
Number: 1             
IDChromosomeStartEnd
GH13I113647chr13114301216114302896
Enhancer Sequence
TCACTGAAAA TTCCAATAGA AGACTAGTTT TAGAAGAATC ATTTTTTCCT AATCTTGAAT 60
TACCATAAGC ATATCGAGGG TTGTGGAACT TACATAAAAC TACGGGCAGT CGTGCCTCAG 120
AGGGCTCTGT GTGGGTGCAT GTGCAGCCAG CACCTGCGGG TGCACCGTGG CTTCCCGTGG 180
CGAGCTTCCT GTGCCTGTGT TTCTTCCAGG CCTTGGGGGT TGAAACTCAG GGCTGGTGAT 240
TCTGAAGGGT GGGGCAGGAG CAGCCCCCGG CTTTATCAGG AAGGGGCTCT GATCGGGCAC 300
GGGGGTGCCC CTGTGGGTGG GATTGCTGGA GCCCAGGACA TCAAGGCCAG CCTGGGCAGC 360
ATAGAGAGAC CCTGCCTCTG AAGAAAGAGT GGGGCTCTGG TGTCCATGGA GAGTCTGGGG 420
AGGGAGGAAG AGGCTAGGGT TCTGAGGGCC TGGAGATGGG GGCTCTGGGT GGCCATGGGA 480
CACGTGGCAG GCGTGTTGGG TTCCAGCTGG GTTGGCTTTG AGAGTCTGGT GGGATGAACC 540
CTCATGGCTC CACCGTCACT TTGAGGTGGT GTCACCTCTG ACCTCTGACC TTCAGCATGG 600
CATGACCTCG CTGAGGTGAC CCTGGTGTCC CACATATCAC CCTGAGTGTT CTTAATACAC 660
AGTCGAGGGC TGTGTTCATT GGACTATTCT GGTGTCACCG CCCACTTCAT TTCTGTGCCT 720
GGCAGCACTT TTACTCCTGG TTGGGAGCAT GACCGCCTCC CAGTTCAGCT TCCTCCTGCG 780
TCCCAAGTGA GCGGGGCGGC TGTCCTCGAG GACTCCGGGC TCACAGCCAA CCTGCTGGCA 840
CGGCTCGAGG ACTCCGGGCT CACAGCCAAC CTGCTGGCAC GGCCGCCCTT TCCCGCCCTG 900
CCTCGGGTGA GCCAAGGACT TGTCTTCTGC TTCCTGGGTT CCTGAAAGAG CTCTCCTCTG 960
ATTTCTCAAA GGCAAAATAA AACTCAGATT TAAGTCTTTG GTGCGTAGCC CCTAATTTCC 1020
TTCCCTTTCT CTGAATCCTC ACTGCCCAGC ATGATGGACC GGCCTGGGCT CAGGACCTGA 1080
TTCCACAGGC TCCCAGCCCT CCCACAGGTA CCGTGTCTTC TGTGCTGGTG TCGCACCCGC 1140
CGGCCACCGC CACCCTGCGT CTTAGACGTC CCGCCGCAGC TGTGTTTCCA CCTCATCTCC 1200
AGCTTGAGTG GCAGCCAGCG GCGCCACCTG CACACGAGCC CCCTCCATTC GAGAAGCACA 1260
GACTATGAGT GTGGCCACGC GTCCCATGAC GTGAACTCAC GTCTGCGCCG AGACCTTTGC 1320
CGGCGGTTTT TTACTGACGG AGTAAGCACT GGAGATGCTT GGTACAGCGT CTTCCATCGG 1380
TAAATTGATT TAGTTAACCT TACAACATAT 1410