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

TagContent
EnhancerAtlas ID
HS141-05338 
Organism
Homo sapiens 
Tissue/cell
NB4 
Coordinate
chr13:76081350-76082730 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MyogMA0500.1chr13:76082656-76082667GACAGCTGCTG+6.14
NFYBMA0502.1chr13:76082003-76082018CTGATTGGCTCATGG-6.71
Tcf12MA0521.1chr13:76082656-76082667GACAGCTGCTG+6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr137608144776081497
chr137608214076082255
Enhancer Sequence
CCACACCTGC CCAGGGTGAG CCAGGCGTGG AGCAGCAAGG GGTGTGTGGG TGAGCAAATG 60
CAGGGTCCAG CCACTGCACA CAGCCAGGCA TGCCAGCTGC TGTGTTGGGG CAGGCAGCTC 120
CAGATGCTGG CACAGGTGCT GGCTCCAAGC AAGGCTGCAG TTGGGCCAGA TACACTGCAC 180
ACAGTTTCTG CTGTGGGCAC CCGCATCTGG ACAAGGGGGA TGTGGTGGCA TCCAGAAGCT 240
TGGAGACAGC AGGGACTGCA GAGACCCAAA GAGGGTGTCA CAGCTCTGGC TTGGTGAGCC 300
CCTAGGTCTG GGATCCCGGA AGGGCCACAG CTCTTCTCTC CTTGTCTCCT TCTCATCACC 360
CACAATGTGG CAAGCGGTGG GGGCTGGGGG GTGTGTTTCA GCCCTGTTTA TGTTATAACT 420
CTTTCAGTCC CACTATTCAG TGAGTCTCAA GTTCTTTTCC CAAGTCCAGG AAGAATGAGG 480
TATGGGGACA GCTGTAGGGT GAGCAAGGTG GAGAGGAGCT TCATTGAGCA ACAGAACAGC 540
TCCCAGGAGA CCTAAAGTGG GTAGTTCCTT CTGGCAGTTG GTAGTCCTGA TGTCTGTGTG 600
AGTCTGGCTG AGTCTCTGGG GTTTTTATGG GTTCCGAAGA GAGGAAGTGC ATACTGATTG 660
GCTCATGGGC GGCCACGGGC AGGCTGGGAA AAGCACCATA AGTTGTCACT CTGGGCTGCA 720
AACTCCACCC TGAACTAGTA GCCTGGTCCC CCAGGCTTCA GGCCATCCCT GGCTTGAAAG 780
TGGAGTTTCA CTGGGGACCC ACCAATAACC TGTCTGCCTC CTGCCATCAA CATGCCATCC 840
AAGGTGCCCA AGCTGTTCAT GCCAAAGGGT GCCTGCAAGC CTGTGCTGAG CTGCCCTCAG 900
CTCCCCTTCT GGCTTCCCTC TTGCACTCAT TGGCATCCAA AGTCTGGAGG TGGCAGGGGG 960
CTGGCATGTT AGCATAGCCC TGAGTGCATG CACACCCAGC CAGGTAGCAA CAGCACCCAG 1020
GCTTGGCCAC AACTTTGCTC TGCACCAGAG TGGGTGCCGG GAGCAGGGAG AGGCCAAACA 1080
GTGGGAGCAG GCACTTCCAA GCCTGCAGGG GCAGGGGCTT CCCAGGCCCC TGAGAGCACA 1140
GGAATGCCTG GGTCCAGAGC CGTGGCCAGG CGGCTACAGC TGTATCCAGG AGCACAGGCC 1200
TCCAGTCTTG CCAACTTGGT AGGGGTAGGG CTCCTGCCCC CTACAGAGGT GCAACCCCAG 1260
CTGCACCTCC CACGCTGCAG CCAGCATCTT CGCAGCGGCC ACTCCAGACA GCTGCTGCTG 1320
CCATCATTGG GACACTGGCA AAAACTGAAT AAGAATTGAA GATTAGGTGA CATCAGTGTT 1380