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

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EnhancerAtlas ID
HS139-07567 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr10:100153680-100154950 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr10:100154564-100154585AGAAGAGGGAAGGGAAGAGGA+6.16
ZNF263MA0528.1chr10:100154576-100154597GGAAGAGGAGAGAAAAGAAGA+6.24
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10100153852100154861
Number: 1             
IDChromosomeStartEnd
GH10I098394chr10100153834100154965
Enhancer Sequence
CATTTCCCCT GCTGTTCTGT CGGCCTGAAG CCCCTCCCTC CCTCATCTTA TGTTTTGTTA 60
ACTCCTCTTT GTCCTTTGGG TCTCAGATCA AACACCTCTT CCATGTAGAG GCTTCTCTGA 120
CCCTAGACCA GGCTGTGTCC CGGCTGCTCC TCCTAGCATC ACACTCACGC CACTTCATCA 180
TCATCACTCG CTCTGTGTCT CTCACCCATC AGGACATCTG CTCCGCTCAC TACCGTATCC 240
CCAGCACCTA GCACAGGCAA GCGCTCATCC ATATTTGTTG GAAGAATTAA TGATGGAACA 300
GATTACTTAA AGATCACAAA CGGAGCACTG GTTAAGCCTC CCAGGGATCC GAAGAGAAAA 360
GGGCAGGAGG CCCCAGCTGG AAGATCCAGA TTGGCTGGTA GATCACAGCT TGGCCAATGT 420
GTGGCAACTG CTGCCAAGCC CCCATCTCCA TCGCCCTGGG GGAATTTGGG GCCGGCTTAA 480
TATGTGTTGA AAAACCACTT CCGAGGGTGT GCTCATCCCT TGAGAGAAAA GCCACGTCGA 540
CGCCTTCTAG CTTCTAGCTT CTAGCTGTAT CTTCTGGTGC ACTGGAAACG GCCCAACCCT 600
TGGCTGCATT CTCCATCCCA ACACACACAC ACACACACAC ACACACACAC ACACACAGCC 660
TTCCATTCCT GCTTCTGCGG GGGCTCATTA AGTCAGACCA CACTGCAGGC TTTGCTGTGT 720
CTGACTGCCA CCTCTCGGAT TGGGCTGTCA GCACAAACCC TCACTCATAA AGAAAAAGGC 780
AGCTTCCTGT CCATCCTGAG GTGTCTGTGT GAGTGTGTAC CAGAGCCCAG GGGAAGGAAC 840
AGTGAGAGAG AAGGGAGAAT GGGCGTTTGC GGGAGTGGAG AGGTAGAAGA GGGAAGGGAA 900
GAGGAGAGAA AAGAAGATAT TAATTTTGAG CTATCAAGCG GGAGGTGGGA GAGAGGCTTT 960
TCTTAGTGAA GCAGTAGGGC ACAGTCACTA AAAAGGAAGA TTTTGGGGAG TCAGACACCT 1020
CAAGCTGGAA ATCAGCCTTG CCACTTACCA GCTGAGTGGC TTTGGGCAAG ACACTCCCTT 1080
CTCTGAACCG CAGTTCTCAG ATGTTGCTCT GAGGGTTAAG TGGATCGTGT GTGATGTGCC 1140
TGGCTCGGTT CCTGGCTCAC TGGGTGAGCT CTGTTAAGTG GCAGCTGTTG TTGCTGCCAC 1200
TGCCACTGTT GTCCTCACTC CTGTTGGGGA ACATGCCCCA CTCCTGTGTC CCACCTCACC 1260
CCCCTCACTC 1270