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

TagContent
EnhancerAtlas ID
HS133-02361 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr1:151537530-151538630 
Target genes
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:151538456-151538474CCTTTCTTCATTCCTTCC-7.88
RREB1MA0073.1chr1:151537593-151537613CCCCACCCCACCCCACCTCG+6.42
ZNF263MA0528.1chr1:151538509-151538530CCCTCCCTTTCACCTTCCTCT-6.16
ZNF263MA0528.1chr1:151538440-151538461TCCTTCTTCCTCTTCTCCTTT-6.21
ZNF263MA0528.1chr1:151538444-151538465TCTTCCTCTTCTCCTTTCTTC-6.32
ZNF263MA0528.1chr1:151538491-151538512CTTTTTCTCTCTCCCTCCCCC-6.38
ZNF263MA0528.1chr1:151538497-151538518CTCTCTCCCTCCCCCTCCCTT-6.66
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1151537867151538409
chr1151537982151538216
Number: 1             
IDChromosomeStartEnd
GH01I151565chr1151537512151538763
Enhancer Sequence
TATTAATCTT GTATATAGTT ATGTCTAACC TGGGATGGGA AGTTCCTCAA GGTTAGGAGT 60
TCACCCCACC CCACCCCACC TCGTGTCTGT ATCCTCACCC TCCCATTCCC CCCAGGTCTG 120
GGATGTAGAA GGCATCAGTA AATGTTTGTT AGACTGAACA GATTGGGTAA GTCTTTCCTG 180
GGAGGGATAA TCCTGGGATC CTGCTTTTCA GTTTTTCCAA AACTCGAGGA CAGAAATGTC 240
CTCAGGAGAG CAGAGCTGTC TCTTTGTGAC TTCGCCCTCA TCCTTTAGAT TCTGAGTTGT 300
ATCCTTGATT TGCATTTTGG TTCAGGCAGA GTCTTGCTCC AGCAGCAGCC CCTGCCTTCA 360
TTCCCTTGAG GGGAACAGTG GCCCAGCAGC TGGTGCAAGG AAAGTTCTTT GTCTTGGGCA 420
TGCACTTGTG TGGTGGAAAT TACCTAATTT TTGCTTTGGC TGAAGGTAGG TCTTTCAGTG 480
CTTGAGCTCA CATCTGGCTG GTGGGAGCTA CTTTGTCAGG TATCAGAAGA ACCTAATGTG 540
TGCAGAGACT GGCCCAAAGT CCAGCCCCCT TGTTTGCACA AACCGGCTGT CATATGATGA 600
ATAATCAGGC TTTGGGTCAG AAATAATTGA AAAAGATCTT CCCTTTGTAA TTTTTGCTTT 660
GTCAAACTTT ATCAGGATCC CTGGGGGCAA GGGAAGCTCT TTGTTTGTGG CAGGCAGCTG 720
CATGTATTCC CTGGCTAAGA AGAATGGGCT ACACATACTT TTCCATCTGC TGAAAGATTT 780
TAGCCTGAGG TTTTTTTCAT CCTCCCTACA AGACTTTCAA GGCCCTTTCA AGGCCGCATA 840
ACATCTCTCC ACCCCCTCTT GTTTCTATTT TCTCATGGAA CGCTAGAAAT CTTTTCTTCT 900
TTCGCTTCGT TCCTTCTTCC TCTTCTCCTT TCTTCATTCC TTCCTTTTTC TCCCTCCCTT 960
TCTTTTTCTC TCTCCCTCCC CCTCCCTTTC ACCTTCCTCT CCCTCTCCCT GTCCTTCTCT 1020
TTCTAAGATT TGAGTGTTAG GAGAATAATG TTTCAAAGTT GGTTGCTTTC ATCTGTTTTA 1080
ACTACCAATT TTATTTTTCT 1100